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Arthrex, Inc. logo
Arthrex, Inc.Ave Maria, FL
Requisition ID: 64180 Title: QA Specialist II - Sterilization Division: Arthrex Manufacturing Inc (US02) Location: Ave Maria, FL Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a QA Specialist II, Sterilization for our manufacturing site in Ave Maria, FL. The QA Specialist II maintains Arthrex Manufacturing Inc (AMI) Sterilization Facility's quality assurance program in accordance with Quality Systems Requirements. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better. Duties and Responsibilities: Ensure proper and timely accurate completion of sterile load files of AMI products; Maintain the Sterile Release program for loads produced by AMI and ensure timely and safe product release to meet customer requests; Report and act by opening, disposition, evaluating, and closing on Non Conformances observed during sterilization processes for AMI to provide a resolution for the disposition of affected loads; Support the AMI Sterilization Facility Personnel to investigate Non Conformances related to sterilization processes in order to determine the root cause and prevent re-occurring issues; Support the AMI Sterilization Facility program to identify and encourage process improvement; Maintain procedures related to the Quality Assurance - Sterilization department activities and review procedures / records related to the AMI Sterilization Facility processes; Function as lead auditor and/or subject matter expert for quality management system audits of Arthrex's sterilization service providers in accordance with applicable standards, e.g., ISO 13485, ISO 11135, ISO 11137 parts 1 and 2, and international regulatory directives; Generate and execute protocols for sterilization processes (i.e. EO, Gamma, X-Ray etc.) and equipment validation and re-validations, along with reports and conclusions; Manage all activities related to sterilization validations and/or testing, and directly interact with external and corporate laboratories, and sterilizers personnel to accomplish the assigned tasks; Assess devices for compatibility to proper sterilization modalities, e.g., radiation and ethylene oxide, by validating and/or adopting Arthrex manufactured products to established or new families using microbiological and sterilization theory and practice according to applicable ISO requirements; Effectively work within a cross functional team environment as both a champion and team member; Support Arthrex business and expansion goals; Must be able to travel domestically and internationally up to 10% of the time Education and Experience: BS in STEM discipline 2+ years relevant experience Skills and Knowledge: Knowledgeable of FDA and ISO guidelines for the sterilization modalities of medical devices required. Manufacturing process knowledge preferred. Project management and communication skills training preferred. Working knowledge of sterilization test systems requirements. Hands on experience managing sterilization product assessments and validations. Test protocol and report writing experience. Knowledge of ISO 13485 guidelines and principles of quality requirements Experience with CAPA processes and non-conformance investigation techniques to determine root-cause Knowledge and Skill Requirements/Specialized Courses and/or Training: Experience in project management, risk management (such as FMEA, FTA, FMECA) tools are highly desirable. Experience in working in Medical Device industry, CAPA, Complaint Management, and Nonconformance Reporting required. Machine, Tools, and/or Equipment Skills: Proficiency in the use of Personal Computers and computer programs, particularly the Microsoft Office Suite; Excel, Word, PowerPoint (or equivalents if changed by the Company). SAP and / or Pilgrim Quality Data experience desirable. Reasoning Ability: Ability to identify opportunities, collect data, analyze established facts, draw valid conclusions, and implement change. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Mathematical Skills Ability to comprehend and apply mathematical principles to the degree required to perform the job based upon job requirements. Language and Communication Skills: Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required sit; use hands and fingers, to handle, or feel; and reach with hands and arms. The employee must occasionally lift and/or move up to 20 pounds. Arthrex Benefits Medical, Dental and Vision Insurance Company-Provided Life Insurance Voluntary Life Insurance Flexible Spending Account (FSA) Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness) Matching 401(k) Retirement Plan Annual Bonus Wellness Incentive Program Free Onsite Medical Clinics Free Onsite Lunch Tuition Reimbursement Program Trip of a Lifetime Paid Parental Leave Paid Time Off Volunteer PTO Employee Assistance Provider (EAP) All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law. Making People Better at Arthrex Lorem ipsum dolor sit amet consectetur. Cras fringilla elementum odio velit. Job Details Date: Dec 7, 2025 Requisition ID: 64180 Salary Range: Job title: QA Specialist II - Sterilization Arthrex Location: Ave Maria, FL, US, 34142 Nearest Major Market: Naples Job Segment: QA, Quality Assurance, Medical Device, Orthopedic, Business Process, Technology, Quality, Healthcare, Management

Posted 30+ days ago

Lonza, Inc. logo
Lonza, Inc.Portsmouth, NH
Location: Portsmouth, NH Join our Quality Assurance team and play a key role in ensuring GMP compliance and operational excellence. You'll be part of a collaborative environment where your expertise helps deliver life-changing therapies. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Competitive compensation programs that recognize high performance. Medical, dental, and vision insurance. Access to our global benefits: https://www.lonza.com/careers/benefits . What you will do: Provide real-time Quality Assurance support on the manufacturing floor. Review GMP documentation and observe operational practices. Offer guidance on routine and non-routine GMP issues. Respond to QA hotline calls and escalate complex issues. Authorize equipment release and manage quality tag-outs. Apply data integrity principles in all aspects of work. Represent QA in meetings and project teams. What we are looking for: Bachelor's degree in a science-related field or equivalent experience. 5-10 years of cGMP experience in a regulated environment. Strong understanding of GMP and ICH guidelines. Familiarity with systems such as TrackWise, SAP, LIMS, and Microsoft Office. Ability to identify and escalate quality issues promptly. Collaborative mindset and commitment to continuous improvement. Excellent communication and problem-solving skills. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Posted 30+ days ago

Global Payments Inc. logo
Global Payments Inc.Georgia, AL
Every day, Global Payments makes it possible for millions of people to move money between buyers and sellers using our payments solutions for credit, debit, prepaid and merchant services. Our worldwide team helps over 3 million companies, more than 1,300 financial institutions and over 600 million cardholders grow with confidence and achieve amazing results. We are driven by our passion for success and we are proud to deliver best-in-class payment technology and software solutions. Join our dynamic team and make your mark on the payments technology landscape of tomorrow. At this time, we are unable to offer visa sponsorship for this position(H1b/OPT). Candidates must be legally authorized to work for any employer in the United States (or (applicable country) on a full-time basis without the need for current or future immigration sponsorship QA Engineer (AI/ML) (Exempt) Enterprise AI/ML Organization Reports to Leader of ML Engineering Group OVERVIEW This QA Engineer position is for a hands-on professional with experience in testing and automating AI/ML pipelines. The ideal candidate is someone who has worked closely with machine learning engineers and data scientists to ensure the quality and reliability of AI/ML models and systems. You will join a dynamic team passionate about innovation, learning, and applying cutting-edge technologies to deliver high-quality AI solutions. RESPONSIBILITIES Develop and implement QA strategies tailored for AI/ML solutions, including models, APIs, pipelines, and agent-based architectures. Create and maintain automated and manual test cases for model validation (accuracy, bias, robustness, explainability, drift). Collaborate with AI engineers, data scientists, and product teams to define success criteria, acceptance standards, and performance metrics. Validate model outputs and system behaviors against business and ethical guidelines. Perform regression, integration, stress, and adversarial testing of AI models and systems. Identify, log, and track bugs and anomalies, ensuring timely resolutions. Support monitoring production AI systems to detect model performance degradation (concept drift, data drift, hallucinations). Ensure compliance with internal AI governance standards, responsible AI principles, and regulatory requirements. Contribute to building automated AI testing frameworks, pipelines, and synthetic data generation systems. Document testing procedures, results, and quality assessments clearly and effectively. Must Haves: Bachelor's degree in Computer Science, Engineering, or a related field. Minimum 6 years of experience in quality assurance, specifically testing AI/ML applications. Experience with the following: Hands-on skills with Python and relevant AI/QA libraries (Pytest, Unittest, Great Expectations, MLflow, Deepchecks, etc.). Familiarity with machine learning frameworks (TensorFlow, PyTorch, or scikit-learn). Experience with test automation tools and frameworks. Knowledge of CI/CD tools (Jenkins, GitLab CI, or similar). Experience with containerization technologies like Docker and orchestration systems like Kubernetes. Familiarity with version control systems like Git. Strong understanding of software testing methodologies and best practices. Excellent analytical and problem-solving skills. Excellent communication and collaboration skills. Global Payments Inc. is an equal opportunity employer. Global Payments provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex (including pregnancy), national origin, ancestry, age, marital status, sexual orientation, gender identity or expression, disability, veteran status, genetic information or any other basis protected by law. If you wish to request reasonable accommodations related to applying for employment or provide feedback about the accessibility of this website, please contact jobs@globalpay.com.

Posted 2 weeks ago

Alo Yoga logo
Alo YogaCommerce, CA
Back to jobs Manager - QA Lab Commerce, California, United States Apply WHY JOIN ALO? Mindful movement. It's at the core of why we do what we do at ALO-it's our calling. Because mindful movement in the studio leads to better living. It changes who yogis are off the mat, making their lives and their communities better. That's the real meaning of studio-to-street: taking the consciousness from practice on the mat and putting it into practice in life. Overview: This role leads the daily operations of the in-house textile testing laboratories. The manager ensures all testing is completed accurately, on time, and in line with corporate, regulatory, and customer standards. The role also oversees technician training, equipment management, test method alignment, and documentation for both locations. Responsibilities: Laboratory Operations Manage day-to-day workflow for all textile and apparel test requests, including AATCC, ASTM, ISO, and internal methods. Review and release test reports with clear, data-driven conclusions. Set turnaround expectations and ensure on-time delivery of results for development, production, and quality teams. Maintain sample traceability and follow established lab SOPs. Technical Leadership Ensure testing methods are followed consistently across both U.S. and Nicaragua labs. Validate and update standard operating procedures as methods evolve. Train lab technicians on new test methods, equipment handling, safety practices, and documentation. Support troubleshooting and root-cause analysis for test failures and product issues. Equipment and Calibration Oversee all lab equipment, including installation, calibration, and preventive maintenance. Maintain calibration and maintenance records to support audits and customer requirements. Recommend new equipment based on business needs and testing capability gaps. Quality and Compliance Make sure the lab meets internal quality system standards and external requirements such as AATCC, ASTM, ISO 17025 principles (if applicable). Prepare labs for internal and external audits. Maintain proper sample handling, recordkeeping, and data integrity practices. Cross-Functional Support Partner with Product Development, Production, QA, Compliance, and Sourcing teams on testing needs and timelines. Provide technical guidance during material selection, mill evaluations, vendor approvals, and performance claim validation. Support global quality programs by generating testing data and trend analysis. Team Management Lead, coach, and schedule technicians in both locations. Define performance expectations and support growth and development. Coordinate staffing, training, and workload balancing between the two labs. Safety and Housekeeping Ensure labs follow all safety protocols, including chemical handling, PPE, and emergency procedures. Keep lab areas organized, clean, and audit-ready. Required Qualifications Bachelor's degree in textiles, textile chemistry, materials science, chemistry, or a related field. 5-8 years of lab experience in apparel, textiles, or materials testing. Hands-on experience with AATCC and ASTM methods (washability, color fastness, pilling, bursting strength, dimensional stability, etc.). Strong understanding of global regulatory requirements and performance standards. Experience managing technicians and daily lab operations. Solid analytical and problem-solving skills. Experience managing multi-site labs or offshore teams. Familiarity with ISO 17025 or other quality management systems. Knowledge of equipment such as Launder-O-Meter, pilling box, Martindale, tensile/tear testers, spectrophotometers, environmental chambers, and standard laundry equipment. Bilingual English/Spanish is helpful. The base salary range for this position is $80,000-$110,000 per year which represents the current range for the base salary for this exempt position. Please note that actual salaries will vary based on factors including but not limited to location, experience, and performance. As such, on occasion and when applicable, there is the possibility that the final, agreed-upon base salary may be outside of the upper end of the range. Please also note the range listed is just one component of the company's total rewards package for exempt employees. Other rewards may include performance bonuses, long term incentives, a PTO policy, and many other progressive benefits. #LI-ONSITE For CA residents, Job Applicant Privacy Policy HERE. Create a Job Alert Interested in building your career at ALO? Get future opportunities sent straight to your email. Create alert Apply for this job indicates a required field Autofill with MyGreenhouse First Name* Last Name* Preferred First Name Email* Phone Country Phone Resume/CV AttachAttach Dropbox Google Drive Enter manuallyEnter manually Accepted file types: pdf, doc, docx, txt, rtf Cover Letter AttachAttach Dropbox Google Drive Enter manuallyEnter manually Accepted file types: pdf, doc, docx, txt, rtf LinkedIn Profile Are you legally authorized to work in the United States without employer support or sponsorship? * Select... Will you require sponsorship to work in the United States at any time in the future? * Select... Are you currently based in the greater LA area and are you comfortable working onsite full-time? * Select... Submit application

Posted 1 week ago

KBI Biopharma logo
KBI BiopharmaDurham, NC
At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact. Position Summary: The Quality Systems team is responsible for establishing and continuously improving the Quality Management System (QMS) that supports the site and Global Compliance activities ensuring systems and business processes are robust, effective, and efficient to comply with required regulations, policies, and guidelines governing the manufacture and holding of materials for our company. The Quality Systems departments goal is support of the site teams to achieve a culture of ongoing regulatory readiness and sustained compliance that delivers safe, pure and effect materials to our clinical and commercial clients. The Senior Quality Assurance Specialist- Client Support is a key Individual Contributor and client projects leader on the Quality Systems team, serving as the Quality-to-Quality client liaison. The incumbent collaborates closely with counterparts throughout the Quality team, supporting processes required to ensure compliance with internal quality documents, regulatory requirements, and cGMP for early and late phase clinical and commercial manufacturing. The incumbent will be responsible for providing support for such activities as product release, deviation, complaint and supplier investigation and closure and facilitating associated collaborations. Additionally, the incumbent will support the compilation, analyzing and reporting of associated metrics. The role requires routine interactions with all functions supporting the external network, including interaction with functions across the company's global network. This role is an onsite hybrid role, working a schedule Monday through Friday between the hours of 8:00 am- 5:00 pm. Responsibilities: Serves as QA facilitator for the Quality aspect of client projects: accountable as the Quality lead, actions coordinator and delegate for the site client project team, joint QA and related meetings. Provides interface between KBI Quality and client regarding batch status, Quality metrics, and Quality issues impacting batch disposition and disposition timeline. Communicates client concerns to KBI teams; facilitates discussions as necessary to resolve client issues. Escalates issues to leadership as needed. Interfaces with the PMO team to ensure Quality topics are addressed. Supports Batch disposition, fully executing the disposition process as needed. Supports audit / inspection readiness of the site. Participates in regulatory and other quality/compliance report-outs; reviews client audit outcomes to ensure appropriate corrective actions are implemented as assigned. Works with Global Compliance to support Client Audits Supports Deviation Management activities by participating in investigational meetings, activities, writing and approving investigation as needed. Assists with compiling, reviewing/ approving Quality Systems and Compliance documentation and reports. Demonstrates knowledge of Quality Systems and functions supporting drug or related FDA governed manufacturing obtained from professional Quality roles. Includes a balance of, from such areas as Supplier Quality Assurance, Compliance, Audits/Inspections, Shop Floor Support, Batch / Material release, Quality document control, review and approval, Validation, QC, Deviations, audit support. Demonstrated ability to keep Project Leads, such as PMs and team members, informed of the status of assigned work. Ability to determine where escalation is necessary. Capability of being flexible as required tasks change and maintain productivity. Requirements: BS/BA Degree in Science or Engineering relevant to the pharmaceutical / Life Science or related industries AS/AA acceptable with 5-7 years of relevant experience as described below. Minimum 5 years prior experience in the Pharmaceutical/Biotechnology industry with a thorough knowledge of Quality Systems, Quality Assurance, and Quality Operations including solid knowledge of global GMP Quality and Regulatory requirements. Minimum of 2 years of previous experience in QA and in a Client-Facing QA or Project Management role Ability to communicate in customer-facing forums to progress issues and obtain positive results. Ability to work professionally with others and facilitate positive interdepartmental interactions with a diverse group of people. Includes ability to navigate conflict to achieve deliverables and drive to targeted outcomes, as well as to resolve differing perspectives with effective negotiation. Listens and is attentive to others' ideas and contributions. Demonstrated ability to be a strong, dependable team-player, yet effective at advancing assignments and projects independently. Voluntarily communicates needs and suggestions clearly and effectively. Demonstrated strong attention to detail and effective investigation, problem solving, and organizational skills. Ability to properly prioritize tasks and manage time effectively. Proactive approach to drive tasks to completion. Excellent written and verbal communication skills. Ability to read, write, and proofread technical documents, investigations, regulatory documents, etc. Ability to compile and analyze data and information from multiple sources Ability to perform basic calculations and data assessment, simple statistics, graphing, plotting data Minimum intermediate proficiency with of Microsoft Office Excel, Word, PowerPoint (Microsoft365). Intermediate proficiency with ERP and QMS systems required, such as SAP, TrackWise, and LIMS p Ability to sit for extended periods of time. Ability to work on site in a manufacturing environment periodically. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Posted 30+ days ago

Lonza, Inc. logo
Lonza, Inc.Portsmouth, NH
QA Specialist III-Operations Onsite in Portsmouth, NH Join Lonza and help us shape the future of life sciences. As a Quality Assurance Specialist III, you will play a key role in reviewing and approving GMP documentation to support our operations and ensure compliance. What you will get: Competitive salary and comprehensive benefits package Opportunities for professional growth and development Collaborative and inclusive work environment Access to cutting-edge technologies and global projects Support for work-life balance Employee recognition programs Health and wellness initiatives What you will do: Review and approve GMP documentation for site operations Serve as QA Subject Matter Expert for equipment and validation documents Ensure compliance with Lonza documentation standards and procedures Collaborate with internal teams to resolve documentation issues Participate in interdepartmental projects and routine meetings Apply data integrity principles in all aspects of work Provide training and mentorship to junior team members What we are looking for: Bachelor's degree in a scientific field 5-10 years of experience in Quality Assurance and GMP environments Strong understanding of GMP regulations and documentation processes Excellent communication and collaboration skills Ability to manage multiple priorities effectively Proficiency in enterprise systems and Microsoft Office tools Business fluent in English About Lonza: Lonza is a global leader in life sciences, dedicated to enabling a healthier world. Our work impacts millions of lives every day. Lonza is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Ready to shape the future of life sciences? Apply now.

Posted 3 weeks ago

Wolters Kluwer logo
Wolters KluwerMadison, WI
Wolters Kluwer's ftwilliam.com platform empowers professionals to streamline Defined Benefit (DB) plan compliance testing, valuation, and proposal generation. As an Industry Solutions Consultant- DB Compliance QA, you'll play a critical role in ensuring our solutions meet the highest standards of accuracy and functionality. In this position, you'll leverage your expertise in ERISA regulations and plan design-covering DB plans, DB/DC combo plans, and cash balance plans-to influence feature design and perform rigorous testing. Working within an agile team, you'll help deliver enhancements that make a real impact for our customers, ensuring every release is reliable, compliant, and user-focused. You will report to the Manager, Consulting- Industry Solutions and work a hybrid schedule (2 days in office, 3 days from home) from one of our local offices. Responsibilities: Collaborate with the product owner and development team to refine user stories before development begins Create sample plans, expected results, and acceptance criteria for new features Perform comprehensive testing of new features and document all tests conducted, including manual and automated tests Ensure software functionality aligns with ERISA laws and regulations Stay current with ERISA laws, regulations, and industry standards Maintain detailed documentation for future testing of similar features and enhancements Identify and suggest software improvements during the testing process Keep up to date with best practices in testing methodologies and tools Work closely with other Industry Solutions Consultants to develop consistent testing policies and procedures Qualifications: ASPPA Credential, such as QPA, or NIPA Credential At least 3 years of experience working with peer review in retirement services 1 years of experience working in a development QA environment Experience with customer support is a plus Familiarity with various project management and workflow tools Experience with ftwilliam.com DB Compliance software is a plus Detail oriented Quick learner and self-starter Ability to multi-task Ability to work well in a team Ability to perform well under pressure Ability to perform well with minimal supervision #LI-Hybrid Benefits: A comprehensive benefits package that begins your first day of employment. Additional Information: Wolters Kluwer offers great benefits and programs to help meet your needs and balance your work and personal life, including Medical, Dental, & Vision Plans, 401(k), FSA/HSA, Commuter Benefits, Tuition Assistance Plan, Vacation and Sick Time, and Paid Parental Leave. Full details of our benefits are available - https://www.mywolterskluwerbenefits.com/index.html Diversity Matters: Wolters Kluwer strives for an inclusive company culture in which we attract, develop, and retain diverse talent to achieve our strategy. As a global company, having a diverse workforce is of the utmost importance. We've been recognized by employees as a European Diversity Leader in the Financial Times, as one of Forbes America's Best Employers for Diversity in 2022, 2021 and 2020 and as one of Forbes America's Best Employers for Women in 2021, 2020, 2019 and 2018. In 2020, we placed third in the Female Board Index, and were recognized by the European Women on Boards Gender Diversity Index. Wolters Kluwer and all of our subsidiaries, divisions and customer/departments is an Equal Opportunity / Affirmative Action employer. Applicants may be required to appear onsite at a Wolters Kluwer office as part of the recruitment process.

Posted 2 weeks ago

Unilock logo
UnilockBrewster, NY

$23+ / hour

Unilock is North America's leader in premium concrete paving stones and retaining walls. We're a family-owned company with over 50 years of success-and we're growing! We're seeking a Quality Assurance Technician to ensure our products meet the highest quality standards. This is a great opportunity for a detail-oriented team player looking to build a long-term career in manufacturing. Responsibilities: Inspect and test products to ensure they meet quality specifications. Perform quality checks, color verification, and sieve analysis of aggregates. Identify and report defects or irregularities in real time. Work closely with production teams to support continuous improvement. Lead daily quality discussions and report on prior-day performance. Conduct 5S audits and support housekeeping standards. Lift up to 50 lbs. and perform standing, bending, and reaching tasks. Support additional duties and special projects as assigned. Qualifications: High school diploma or GED required (manufacturing experience a plus). Strong attention to detail and commitment to quality. Basic mechanical aptitude. Reliable attendance and safety-focused mindset. Ability to rotate to night shift as needed. English proficiency required. Benefits: Competitive pay at $23/hour Health benefits starting the first of the month after hire Paid time off, paid holiday shutdown (Christmas-New Year's) 401(k) with company match and profit sharing Semi-annual and year-end bonuses Career growth in a family-oriented workplace Apply today and build your future with Unilock!

Posted 1 week ago

ICF International, Inc logo
ICF International, IncColumbia, MD

$55,388 - $94,160 / year

QA/QC Inspection Specialist, Energy Efficiency (Field) Utilities Programs and Services Location: Maryland (Remote- Home Office with Local Travel) Ready to make a Difference? ICF is seeking a Quality Assurance Specialist, based in Maryland to assist in the delivery of residential energy efficiency programs. We are seeking a Quality Assurance Specialist to conduct comprehensive energy efficiency quality assessments in accordance with utility program standards in Maryland. We place a premium on the ability to work independently when necessary but to function as part of a team, a drive to succeed, and a commitment to client satisfaction. Why you will love working here: Quality of life: Flexible workplace arrangements, work-life balance Investment of community: Donation matching, volunteer opportunities Investment in you: Tuition reimbursement, access to professional development resources, 401k matching, Employee Stock Purchase Plan And many, many more(Ask your recruiter for more details!) What you will be doing: Conduct QA/QC assessments in residential homes in accordance with program guidelines Complete detailed and accurate field inspections verifying quantities and technologies aligning with utility rebate applications Interact with contractors and homeowners answering questions regarding energy efficiency and additional energy savings opportunities Contribute to the evolution of program strategies and the design of program features and services Contribute to the deployment of program marketing and outreach campaigns Coordinate with or schedule QA/QC activities such as field inspections Prepare summary reports identifying additional opportunities found during QC visits Must have a reliable vehicle for local travel. Requirements are between 60% to 80% of the time. (reimbursement for mileage provided) What we need you to have (minimum qualifications): Bachelor's Degree in (business, energy, communication or related studies preferred) (candidates can substitute one year of experience for each year of education) 1+ Years of professional work experience; preferably in energy efficiency with an understanding of residential construction Must have a clear and clean driving record and pass drug and background check Basic mechanical skills and able to lift boxes no heavier than 30 pounds, climbing stairs and ladders, driving, walking, standing, above head arm movements What we would like you to have: Experience working with MHIC licensed companies Great interpersonal skills Ability to promote energy efficiency practices in the residential sector preferred Experience performing residential inspections Experience with energy efficiency technologies and practices is highly desirable Experience working on successful energy efficiency programs Proficient with suite of Microsoft Office tools such as Excel, PowerPoint, Outlook, etc Customer service and/or sales conversion experience. Working at ICF ICF is a global advisory and technology services provider, but we're not your typical consultants. We combine unmatched expertise with cutting-edge technology to help clients solve their most complex challenges, navigate change, and shape the future. We can only solve the world's toughest challenges by building a workplace that allows everyone to thrive. We are an equal opportunity employer. Together, our employees are empowered to share their expertise and collaborate with others to achieve personal and professional goals. For more information, please read our EEO policy. We will consider for employment qualified applicants with arrest and conviction records. Reasonable Accommodations are available, including, but not limited to, for disabled veterans, individuals with disabilities, and individuals with sincerely held religious beliefs, in all phases of the application and employment process. To request an accommodation, please email Candidateaccommodation@icf.com and we will be happy to assist. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations. Read more about workplace discrimination rights or our benefit offerings which are included in the Transparency in (Benefits) Coverage Act. Candidate AI Usage Policy At ICF, we are committed to ensuring a fair interview process for all candidates based on their own skills and knowledge. As part of this commitment, the use of artificial intelligence (AI) tools to generate or assist with responses during interviews (whether in-person or virtual) is not permitted. This policy is in place to maintain the integrity and authenticity of the interview process. However, we understand that some candidates may require accommodation that involves the use of AI. If such an accommodation is needed, candidates are instructed to contact us in advance at candidateaccommodation@icf.com. We are dedicated to providing the necessary support to ensure that all candidates have an equal opportunity to succeed. Pay Range- There are multiple factors that are considered in determining final pay for a position, including, but not limited to, relevant work experience, skills, certifications and competencies that align to the specified role, geographic location, education and certifications as well as contract provisions regarding labor categories that are specific to the position. The pay range for this position based on full-time employment is: $55,388.00 - $94,160.00 Maryland Remote Office (MD99)

Posted 3 weeks ago

Lonza, Inc. logo
Lonza, Inc.Portsmouth, NH
Location: Portsmouth, NH (On-site) Join Lonza's Quality Operations team and play a key role in ensuring compliance and excellence for our customers. As a QA Project Manager II, you will act as the primary liaison for quality-related matters, driving collaboration and delivering solutions that make a real impact. What you will get: An agile career and dynamic working culture An inclusive and ethical workplace Competitive compensation programs that recognize high performance Medical, dental, and vision insurance Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits What you will do: Serve as the primary QA liaison for assigned external customers Manage quality processes including change controls, deviations, investigations, and CAPAs Lead Joint Quality Team meetings and track action items Review and approve investigation reports and root cause analyses Collaborate with internal teams such as MSAT, Manufacturing, Engineering, and QC Support customer audits and maintain compliance with data integrity principles Prepare and present customer metrics and KPIs What we are looking for: Bachelor's degree in a scientific field or equivalent experience Experience in GMP environments and Quality Assurance (5+ years preferred) Strong understanding of biotechnology manufacturing and project management Ability to analyze data, make sound decisions, and prioritize tasks Excellent communication and relationship-building skills Familiarity with cGMPs and regulatory requirements A proactive, detail-oriented approach with a commitment to quality About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Posted 30+ days ago

Lonza, Inc. logo
Lonza, Inc.Tampa, FL
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of . Key Responsibilities: Execute and document validation activities (IQ, OQ, PQ, PPQ), including risk assessments and periodic reviews. Support the full Validation Life Cycle-from design through revalidation and continuous improvement. Collaborate with internal and external teams to ensure new systems meet cGMP and validation requirements. Maintain and update validation-related documentation (SOPs, Change Controls, CAPAs, Deviations). Assist in investigations and resolution of deviations involving equipment, systems, and processes. Provide validation support during audits and ensure inspection readiness Key Qualifications: Bachelor's degree in engineering, life sciences, or related field 2-5 years of validation experience in a GMP-regulated environment. Cross- Functional Communication Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Posted 30+ days ago

Huntington Bancshares Inc logo
Huntington Bancshares IncColumbus, OH
Description Description Huntington Bank is looking for a QA Test Automation Lead in our Data Lake and Data Warehouse team. In this role you will be part of a team working to develop solutions enabling the business to leverage data as an asset at the bank. As a QA Test Automation Lead, you will work to develop automation test strategies and frameworks ensuring all IT SDLC processes are documented and practiced, working closely with multiple technologies teams across the enterprise. Key technologies include Azure DevOps, Python, AWS S3, Snowflake, Zena, and DataStage. If you consider data as a strategic asset, evangelize the value of good data and insights, have a passion for learning and continuous improvement, this role is for you. Key Responsibilities Lead quality assurance efforts for multiple concurrent projects focused on data ingestion and integration, ensuring alignment with banking regulatory standards. Design, implement, and maintain automated testing frameworks and CI/CD pipelines to support scalable and secure data operations. Develop and execute comprehensive test strategies covering System Integration Testing (SIT) and closely partner with the team for User Acceptance Testing (UAT). Collaborate with data engineers, developers, project managers, and compliance teams to ensure data quality, integrity, and traceability throughout the ingestion lifecycle. Drive continuous improvement in QA processes Design and implement a scalable test automation framework and strategy. Create daily/weekly test execution metrics and status reporting. Assist the Project Managers/Scrum Masters to drive project team to defect resolution. Leverage existing tools/techniques to streamline and automate wherever possible. Actively participate in walk-through, inspection, review and user group meetings for quality assurance. Actively participate in the review of project requirements, data mappings and technical design specifications. Analyze data, troubleshoot data issues, and create action plans to address data quality issues. Collaborate with project team on defect analysis and triage. Participate in production implementation verification and being accountable for validating system quality Basic Qualifications Bachelor's degree 5+ years of ETL testing experience in data warehouse environment 3+ years of test automation experience 2+ years of experience with Snowflake and AWS 2+ Experience leading QA Analysts on a project team Preferred Qualifications Experience in financial services (banking) industry. Strong experience with SQL, ETL testing, and data warehouse concepts (e.g., star/snowflake schema, OLAP) Proficiency in test automation tools such as Cucumber, Selenium, PyTest, or DBT tests. Experience with cloud data platforms (Snowflake, AWS). Familiarity with CI/CD tools (Azure DevOps). Excellent verbal and written communications skills. Ability to effectively prioritize and execute tasks. Detail oriented and highly motivated with strong organizational, analytical and problem-solving skills. Exempt Status: (Yes = not eligible for overtime pay) (No = eligible for overtime pay) Yes Workplace Type: Office Our Approach to Office Workplace Type Certain positions outside our branch network may be eligible for a flexible work arrangement. We're combining the best of both worlds: in-office and work from home. Our approach enables our teams to deepen connections, maintain a strong community, and do their best work. Remote roles will also have the opportunity to come together in our offices for moments that matter. Specific work arrangements will be provided by the hiring team. Huntington is an Equal Opportunity Employer. Tobacco-Free Hiring Practice: Visit Huntington's Career Web Site for more details. Note to Agency Recruiters: Huntington Bank will not pay a fee for any placement resulting from the receipt of an unsolicited resume. All unsolicited resumes sent to any Huntington Bank colleagues, directly or indirectly, will be considered Huntington Bank property. Recruiting agencies must have a valid, written and fully executed Master Service Agreement and Statement of Work for consideration.

Posted 30+ days ago

True Anomaly logo
True AnomalyDenver, CO

$80,000 - $110,000 / year

YOUR MISSION We are seeking a motivated and detail-driven Software QA Engineer to support testing efforts against our Mosaic product. The ideal candidate has foundational experience in QA, can work independently on well-defined tasks, and is ready to take ownership of test planning and execution. Candidate should be comfortable utilizing automation, and wanting to gain more experience in their automation skills. This role is perfect for someone who has progressed beyond junior-level responsibilities and is ready to contribute more directly to process, automaton coverage and cross team collaboration. RESPONSIBILITIES Develop and execute manual and automated test cases across full-stack Participate in refining requirements and acceptance criteria Understand and perform basic QA testing methodologies Regression Testing Integration Testing / System Testing Exploratory Testing Responsible for defect triage and resolution Contributing to writing test cases manual and automated scripts in playwright Collaborate with developers, product and design for a full software lifecycle deliveries QUALIFICATIONS 2-4 years of experience in software QA Bachelors degree in computer science or related field/equivalent education Solid understanding of QA methodologies and Agile practices Experience with test case management and tooling Proficiency in defect resolution and ticket tooling such as JIRA/Azure Devops/etc. Experience testing APIs utilizing tools like postman or insomnia Proficiency in coding (preferred Javascript) Ability to analyze requirements and convert them to test plans/cases Strong communication skills and ability to work independently with minimal oversight Proficient utilizing github and version control for repositories U.S. Citizen and eligible for DoD Secret or TS/SCI clearance PREFERRED SKILLS AND EXPERIENCE Hands on experience with Playwright Familiarity with CICD pipeline tooling (github actions ) Specifically GRPC API testing Exposure to performance and load testing tooling Experience testing elixir or a similar backend system Motivated to learn and grow within QA industry Team player with a proactive, problem-solving mindset Ability to manage time and tasks effectively in a fast paced environment Flexible mindset/Startup mentality Detail oriented COMPENSATION Base Salary: Denver: $80,000 - $105,000 | Long Beach: $85,000 - $110,000 Equity + Benefits including Health, Dental, Vision, HRA/HSA options, PTO and paid holidays, 401K, Parental Leave Your actual level and base salary will be determined on a case-by-case basis and may vary based on the following considerations: job-related knowledge and skills, education, location, and experience. ADDITIONAL REQUIREMENTS Work Location-Successful candidates will be located near Long Beach, Denver or Colorado Springs. While we observe a hybrid work environment, some work must be done on site. Work environment-the work environment; temperature, noise level, inside or outside, or other factors that will affect the person's working conditions while performing the job. Physical demands-the physical demands of the job, including bending, sitting, lifting and driving. This position will be open until it is successfully filled. To submit your application, please follow the directions below. #LI-Hybrid

Posted 30+ days ago

Blitt & Gaines P.C. logo
Blitt & Gaines P.C.South Phoenix, AZ
Description Job Title: Software QA Analyst Job Summary: We are seeking a motivated and detail-oriented Software Quality Assurance Analyst to join our development team. The ideal candidate has a strong understanding of QA fundamentals, experience translating requirements into effective test coverage, and a willingness to learn and grow within a fast-paced software environment. You will work closely with product owners, developers, and other team members to ensure the delivery of high-quality software solutions. This is an experienced level position. You will report to the Director of Development and work to test a variety of applications and processes for our firm. Key Responsibilities: Review acceptance criteria and requirements to create comprehensive, well-structured test cases. Execute manual and/or automated tests across various applications and environments. Perform comparisons and validations of large datasets to ensure accuracy and data integrity. Assist with the setup, configuration, and maintenance of applications within test environments. Document test results, defects, and reproducible steps using standard ALM tools (e.g., Azure DevOps, Jira). Collaborate with developers and product owners to clarify requirements and ensure alignment with SDLC processes. Participate in test planning, requirement reviews, and release readiness activities. Minimum Requirements: 1+ years of experience in a manual or automated QA role. Demonstrated ability to create test cases from acceptance criteria or requirements. Solid understanding of Software Development Lifecycle (SDLC) concepts. Familiarity with ALM or defect-tracking tools such as Azure DevOps, Jira or similar. Experience comparing and analyzing large datasets using tools such as Microsoft Excel, SQL, or similar technologies. Experience with application setup and configuration within test environments. Preferred Qualifications: Proficiency with Azure DevOps for managing test plans, executing test cases, tracking defects, and collaborating across development teams. Experience using Visual Studio to execute tests, debug issues, analyze logs, and support development workflows. Hands-on experience testing Python applications, including working with virtual environments, dependency management, and common testing tools (e.g., pytest, unittest). Ability to write or maintain automated tests using recognized testing frameworks such as Selenium, Playwright, pytest, NUnit, or xUnit, depending on application stack. Familiarity with version control systems such as Git, including branching strategies and review workflows. Nice to Haves: Experience with QA automation, including scripting or working with testing frameworks such as Selenium, Playwright, NUnit, xUnit, or similar. Exposure to CI/CD pipelines and their role in QA processes. Familiarity with the litigation and/or collections industry, including common workflows and data structures. Exposure to scripting or automation tools (e.g., Python, PowerShell, Bash) Benefits: Blitt and Gaines, P.C. offers PTO, Paid Holidays, Medical Benefits, Competitive Salary and 401k and profit sharing plans! Medical Benefits include - Medical, Dental, Vision, Life Insurance and Short Term Disability.

Posted 3 weeks ago

G logo
Government Technology AgencyNon, OK
[What the role is] Software engineer to support the development of CaseCentral 2nd phase [What you will be working on] We are seeking a talented and experienced Quality Engineer with a passion for automating testing processes to join our dynamic team, focusing on testing Saas-based (e.g. Salesforce) applications for enterprise and government solutions. The ideal candidate will have a strong foundation in SaaS testing methodologies and experience with enterprise platforms and DevOps. You will ensure the quality and reliability of government Saas-based (e.g. Salesforce) applications through comprehensive testing strategies and automation. You will be developing automated testing frameworks, conducting performance testing, and maintaining security compliance as well as integrating testing into CI/CD pipelines and collaborating with engineering teams to optimize test coverage and identify automation opportunities. You will work within an agile development team at the Ministry of Social and Family Development (MSF) to modernise and develop CaseCentral, a case management platform. Your responsibilities include: Test Automation: Develop and maintain robust test automation frameworks (e.g. Playwright) for Saas-based (e.g. Salesforce) applications. Create and execute automated test scripts for web-based SaaS (e.g. Salesforce) applications Collaborate with engineering teams to optimise test coverage and identify automation opportunities Analyse test results and provide detailed defect reports Ensure test compatibility with Saas-based (e.g. Salesforce) platform updates Quality Assurance: Design and implement comprehensive test strategies for enterprise and government SaaS applications Conduct end-to-end testing of Saas-based (e.g. Salesforce) integrations Validate application functionality across different Salesforce environments Ensure compliance with government and enterprise security standards Performance Testing: Conduct performance testing to identify and address bottlenecks for Salesforce-based SaaS applications Analyse performance metrics and provide optimization recommendations Test application behaviour under various load conditions Monitor and report on application performance in enterprise environments DevOps Integration: Integrate test automation into CI/CD pipelines Implement continuous testing practices Implement continuous testing practices to ensure timely feedback and improve product quality. Contribute to the development and maintenance of infrastructure as code (IaC) solutions. Test Planning and Execution: Participate in test planning and estimation activities (includes security testing e.g. penetration testing, vulnerability assessments, compliance verification) Execute manual tests as needed to supplement automated testing. Collaborate with development team members to ensure effective test coverage across functional and security requirements [What we are looking for] Qualifications and Experience Required: A strong background in Computer Science, Computer Engineering, Information Systems Management, Information Technology, or related disciplines. Minimum 3 years of experience in Saas-based (e.g. Salesforce) application testing. Proven experience in test automation development and execution with SaaS, enterprise or government solutions. Experience with DevOps principles and practices. Experience with agile development methodologies and experience working in Agile teams. Strong programming skills in languages i.e. Java, Python. Hands-on experience with test automation frameworks i.e. Playwright, Katalon, Selenium, JUnit Familiarity with CI/CD tools (i.e. GitLab CI/CD) and cloud platforms (AWS) Understanding of CRM systems, preferably Salesforce platform architecture and solutions Knowledge of performance testing tools (JMeter, Gatling).

Posted 30+ days ago

SS&C Technologies logo
SS&C TechnologiesDenver, CO
As a leading financial services and healthcare technology company based on revenue, SS&C is headquartered in Windsor, Connecticut, and has 27,000+ employees in 35 countries. Some 20,000 financial services and healthcare organizations, from the world's largest companies to small and mid-market firms, rely on SS&C for expertise, scale, and technology. Job Description Position Title: Lead Software QA Engineer (Hybrid) Denver CO Get To Know Us: SS&C is leading the way. We continue to look for todays and tomorrow's brightest talent, those that embody a spirit to improve not only their lives, but those around them. From college students to seasoned and experienced professionals, we encourage you to apply. SS&C prides itself on hiring diverse, honest, dynamic individuals, who value collaboration, accountability, and innovation to name a few. Why You Will Love It Here! Flexibility: Hybrid Work Model and Business Casual Dress Code, including jeans Your Future: 401k Matching Program, Professional Development Reimbursement Work/Life Balance: Flexible Personal/Vacation Time Off, Sick Leave, Paid Holidays Your Wellbeing: Medical, Dental, Vision, Employee Assistance Program, Parental Leave Wide Ranging Perspectives: Committed to Celebrating the Variety of Backgrounds, Talents and Experiences of Our Employees Training: Hands-On, Team-Customized, including SS&C University Extra Perks: Discounts on fitness clubs, travel and more! What you'll get to do: Reporting to the QA Director, the QA Lead Engineer will oversee QA testing within an agile project for one of Calastone's products or functional areas. They'll manage all QA activities, providing regular progress updates to stakeholders and highlighting risks or blockers. The role involves close collaboration with Engineering, Product, Operations, and DevOps teams to deliver high-quality applications supported by automated regression tests built in C# using a Behaviour Driven Development (BDD) approach. As the QA Lead, the individual will plan and coordinate testing activities, delegate tasks, and mentor QA Engineers, ensuring industry-standard testing practices are applied. They will also contribute to the QA team's development by sharing knowledge, running learning sessions, and maintaining the QA knowledge base. Success in this role requires a strong grasp of Calastone's technical and functional landscape and a deep understanding of automated testing strategies. What you will get to do: Oversee QA activities and serve as the primary QA contact for the assigned project. Report to the QA Director and ensure the QA Strategy is consistently applied across all relevant projects. Lead the design, development, and maintenance of automated test frameworks built on .NET Core with C# and BDD. Drive the integration of automated testing solutions into the engineering build pipeline (Continuous Integration) using GitHub Actions. Facilitate integration testing between products, using stubs and drivers where appropriate. Mentor, support, and coach QA Engineers and Senior QA Engineers in their professional growth. Monitor and report on automated test coverage, ensuring visibility for key stakeholders. Develop and maintain a Test Plan and Approach for the project, aligned with Calastone's QA Strategy. Prepare QA release documentation in line with Calastone's QA standards. Maintain clear, open, and transparent communication with stakeholders on QA progress, highlighting risks or potential impacts. Conduct exploratory testing to support Calastone's agile delivery approach and align with QA best practices. Build a strong understanding of Calastone's products and functionality. Follow recognised best practices in test automation and quality assurance. What you will bring: Proven experience leading QA teams and managing people, including delivery of high-profile, time-sensitive projects. Strong background in financial technology, with hands-on experience testing financial data, systems, and messaging formats (XML, JSON, FIX, SFTP, Swift). Understanding of the European Mutual Funds and/or Exchange-Traded Funds (ETF) markets (advantageous). Proficiency in object-oriented programming, ideally C# (preferred) or Java, and developing .NET-based automated testing frameworks using BDD tools such as SpecFlow or Reqnroll. Expertise in automating REST API and UI testing with Selenium WebDriver and Playwright (preferred). Experience testing event-driven services, including those using Azure Service Bus and Azure Kubernetes Services (AKS). Skilled in configuring CI/CD pipelines with GitHub Actions workflows (YAML). Strong understanding of QA automation methodologies, tools, and agile processes. Knowledge of testing techniques such as equivalence partitioning and boundary value analysis. Experience with non-functional testing (performance, load, stress), ideally using NeoLoad. Proficiency in writing SQL queries and analysing relational databases. Familiarity with AI tools such as Copilot, LLMs, or MCPs to enhance test automation (advantageous). Competent in Microsoft technologies including Visual Studio, Azure, Word, Excel, and Windows environments. Clear, confident communicator able to engage effectively with both technical and business stakeholders. ISTQB Software Testing certification (or equivalent). Additional attributes we are seeking: Driven, proactive, and committed to delivering results. Adaptable and resilient in a fast-changing, agile environment. Collaborative team member who leads by example and supports others' growth. Passionate about quality, coding best practices, and continuous improvement. Calm, focused, and effective under pressure, with strong problem-solving and analytical skills. Communicates clearly and confidently, both in writing and verbally. Professional, honest, and accountable in all interactions. Takes ownership, follows issues through to root cause, and delivers without micromanagement. Priorities effectively to meet deadlines and achieve outcomes. Open to learning, innovation, and new ways of working. #Digital Worker Enabled# # Initials: &DWRK # # Keywords: LEAD QA Engineer, MS Playwright REST API GitHub Actions Selenium BDD # #Digital Worker Enabled LinkedIn# # Initials: &DWRK # # Keywords: LEAD QA Engineer, MS Playwright REST API GitHub Actions Selenium BDD# Unless explicitly requested or approached by SS&C Technologies, Inc. or any of its affiliated companies, the company will not accept unsolicited resumes from headhunters, recruitment agencies, or fee-based recruitment services. SS&C offers excellent benefits including health, dental, 401k plan, tuition and professional development reimbursement plan. SS&C Technologies is an Equal Employment Opportunity employer and does not discriminate against any applicant for employment or employee on the basis of race, color, religious creed, gender, age, marital status, sexual orientation, national origin, disability, veteran status or any other classification protected by applicable discrimination laws.

Posted 30+ days ago

C logo
Core & Main Inc.Saint Louis, MO
Based in St. Louis, Core & Main is a leader in advancing reliable infrastructure with local service, nationwide. As a specialty distributor with a focus on water, wastewater, storm drainage and fire protection products and related services, Core & Main provides solutions to municipalities, private water companies and professional contractors across municipal, non-residential and residential end markets, nationwide. With over 370 locations across the U.S., the company provides its customers local expertise backed by a national supply chain. Core & Main's 5,700 associates are committed to helping their communities thrive with safe and reliable infrastructure. Visit coreandmain.com to learn more. Job Summary We are seeking a highly skilled and detail-oriented Data and Integrations QA Engineer to join our dynamic Data Engineering team. As a key member of our team, you will play a crucial role in ensuring the quality and reliability of our data pipelines and integrations. Your primary focus will be on testing the end-to-end data flow, identifying, and resolving data quality issues, and ensuring seamless integration between various systems. Major Tasks, Responsibilities and Key Accountabilities Data Quality Assurance: Conduct comprehensive testing of data pipelines to ensure accuracy, completeness, and consistency of data. Develop and execute test plans for data validation, transformation, and loading processes. Collaborate with Data Engineers to understand data models and business rules, ensuring adherence to quality standards. Integration Testing: Validate and verify data integrations between different systems and applications. Perform end-to-end testing of integrated data flows to identify and address potential issues. Work closely with cross-functional teams to understand integration requirements and implement effective testing strategies. Automation: Design, implement, and maintain automated testing scripts for data pipelines and integrations. Continuously enhance and optimize automated test frameworks to improve efficiency and coverage. Issue Identification and Resolution: Investigate and troubleshoot data discrepancies, integration failures, and performance issues. Collaborate with Data Engineers and developers to resolve identified issues and ensure data quality standards are met. Documentation: Document test cases, test results, and testing processes to facilitate knowledge transfer and future reference. Contribute to the development and maintenance of QA documentation, including best practices and guidelines. Preferred Qualifications: Bachelor's degree in Computer Science, Information Technology, or a related field 3+ years experience in data management, data integration, and data lake management 3+ years experience in Microsoft SQL development using T-SQL code to design, implement and optimize database objects, including tables, views, stored procedures, indexes and functions. Experience with Master Data Management Platforms such as Enterworks, Profisee, or Informatica Exposure with Azure data architecture and solid understanding of tools for building data pipelines of cloud-based data platforms including delta lake architecture and data warehousing Understanding of HTTP APIs, testing tools like Postman/JMeter (doc already has API integration) Familiarity with data security, data privacy regulations, and compliance standards. Excellent analytical and problem-solving skills, with the ability to drive data-driven decision-making Experience with testing tools and frameworks, and a strong understanding of automation principles Core & Main is an Equal Employment Opportunity employer. Employment at Core & Main is based solely on a person's merit and qualifications directly related to professional competence. Core & Main does not discriminate against any employee or applicant on the basis of race, creed, color, religion, national origin, nationality, ancestry, age, disability, veteran status, pregnancy or related condition (including breastfeeding), affectional or sexual orientation, gender identity or expression, marital status, status with regard to public assistance, citizenship, or any other basis protected by law. None of the questions in this application are intended to elicit information regarding any protected characteristics, nor imply any limitation, illegal preferences or discrimination based upon non-job-related information or protected characteristics. For more information, please click here or visit https://www.eeoc.gov

Posted 2 weeks ago

August Bioservices logo
August BioservicesNashville, TN
Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! We are seeking a proactive QA Specialist to provide real-time quality oversight across manufacturing, packaging, inspection, and warehouse operations. The role ensures cGMP compliance, supports production activities, and promotes a strong quality culture. The ideal candidate is detail-oriented, hands-on, and able to provide guidance to operators while maintaining inspection readiness. Responsibilities Maintain a daily presence on the production floor to provide real-time QA support and guidance. Ensure adherence to batch records, SOPs, and validated procedures during manufacturing, packaging, and inspection activities. Perform QA line clearances, in-process checks, and AQL inspections, and support visual inspection and automated inspection processes. Act as a Designated Observer for controlled substance handling, ensuring compliance with internal and regulatory requirements. Routinely walk through production, lab, and warehouse areas to assess GMP compliance and escalate issues as needed. Verify labeling issuance, reconciliation, and documentation to ensure proper handling of materials and finished products. Provide on-the-floor coaching and guidance to operators, reinforcing GMP compliance and best practices. Collaborate with Manufacturing and Planning teams to prioritize lot disposition, minimize downtime, and support operational flow. Monitor cleaning, sanitization, and environmental controls prior to critical operations. Promote a quality-focused culture by sharing lessons learned and encouraging proactive issue identification. Maintain knowledge of deviation, OOS/OOT, and CAPA processes to support investigations if required. Assist in gathering facts, reviewing documentation, and providing QA input when deviations occur on the floor. Understand root cause analysis tools (5 Whys, Fishbone, FMEA) to support quality discussions. Review, revise, and proofread GMP documentation, including batch records, SOPs, and logbooks. Support document control processes and ensure training documentation is correctly linked to controlled systems. Ensure compliance with regulatory standards (FDA, ICH, DEA) and Good Documentation Practices. Conduct routine walk-throughs to maintain inspection readiness. Support internal audits and regulatory inspections by providing floor-level guidance and documentation as needed. Qualifications Bachelor's degree in a scientific discipline or equivalent experience. 2-5 years in a GMP-regulated environment, with experience in on-the-floor QA support. Knowledge of cGMPs, FDA/ICH regulations, and QA documentation practices. Familiarity with Master Control or electronic quality systems preferred. Strong communication, problem-solving, and interpersonal skills. Ability to work flexible shifts, including evenings or weekends as required.Preferred Qualifications: Experience with automated visual inspection processes.Knowledge of controlled substance handling.Prior involvement in regulatory inspections. Work Environment & Physical Demands Regular presence in GMP manufacturing and cleanroom environments with proper gowning. Occasional off-shift, weekend, or extended coverage may be necessary. At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule - from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment. We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team! August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Posted 30+ days ago

PwC logo
PwCMontpelier, VT

$99,000 - $232,000 / year

Industry/Sector Not Applicable Specialism Managed Services Management Level Manager Job Description & Summary At PwC, our people in risk and compliance focus on maintaining regulatory compliance and managing risks for clients, providing advice, and solutions. They help organisations navigate complex regulatory landscapes and enhance their internal controls to mitigate risks effectively. As a risk management generalist at PwC, you will provide advisory and practical support to teams across a wide range of specialist risk and compliance areas. Enhancing your leadership style, you motivate, develop and inspire others to deliver quality. You are responsible for coaching, leveraging team member's unique strengths, and managing performance to deliver on client expectations. With your growing knowledge of how business works, you play an important role in identifying opportunities that contribute to the success of our Firm. You are expected to lead with integrity and authenticity, articulating our purpose and values in a meaningful way. You embrace technology and innovation to enhance your delivery and encourage others to do the same. Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to: Analyse and identify the linkages and interactions between the component parts of an entire system. Take ownership of projects, ensuring their successful planning, budgeting, execution, and completion. Partner with team leadership to ensure collective ownership of quality, timelines, and deliverables. Develop skills outside your comfort zone, and encourage others to do the same. Effectively mentor others. Use the review of work as an opportunity to deepen the expertise of team members. Address conflicts or issues, engaging in difficult conversations with clients, team members and other stakeholders, escalating where appropriate. Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements. Minimum Degree Required Bachelor's Degree Minimum Year(s) of Experience 5 year(s) Demonstrates extensive knowledge and/or a proven record of success in the following areas: Quickly and agilely learn client HCP and HCO engagement processes and ways of working, analyzing for opportunities to optimize, develop, update, and govern team playbooks, SOPs, and process documentation to ensure operational consistency and compliance; Develop and maintain training plans for both new and existing team members; Designing and delivering training curricula for new hires and ongoing development for existing team members; Keeping training materials current with process changes, client requirements, and industry/regulatory updates; Managing and delivering structured onboarding programs for new hires to ensure smooth integration and readiness; Providing coaching and skills development opportunities to build functional expertise across the team; Partnering with leadership to identify training gaps and address them proactively; Designing and executing quality monitoring frameworks to evaluate managed services team delivery accuracy, compliance, and timeliness of deliverables; Conducting regular quality reviews of outputs (e.g., tiering assessments, contracting, payment processing); Tracking and reporting quality performance metrics; identify root causes of recurring errors and define corrective actions; Partnering with leadership to implement corrective training and process refinements; Leading process improvement and optimization; Serving as a key SME in continuous improvement initiatives, contributing to best practices across global operations; Mentoring junior team members; Supporting the process design and implementation of new client or new markets ensuring a high-level of customer engagement, quality, timeliness, and service-readiness across all regions; Managing deliverables on or ahead of deadlines and reporting any issues/risks beforehand; Experience in life science meetings & events, pharmaceutical device or healthcare setting working with HCPs, HCOs or Patients; Identifying opportunities for efficiency, automation, and standardization within the managed services delivery model; Working closely with the client-dedicated operations team to streamline processes while maintaining quality and compliance; Communicating with senior leadership and senior client stakeholders; Delivering "white glove" customer service; Ability to work in a fast-paced environment, with a strong emphasis on quality and accuracy; Monitoring and managing other responsibilities not necessarily listed but logically inherent to the role; Leading teams of individuals with a positive attitude; Strong English language reading comprehension and writing skills. Travel Requirements Up to 40% Job Posting End Date Learn more about how we work: https://pwc.to/how-we-work PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy . As PwC is an equal opportunity employer, all qualified applicants will receive consideration for employment at PwC without regard to race; color; religion; national origin; sex (including pregnancy, sexual orientation, and gender identity); age; disability; genetic information (including family medical history); veteran, marital, or citizenship status; or, any other status protected by law. For only those qualified applicants that are impacted by the Los Angeles County Fair Chance Ordinance for Employers, the Los Angeles' Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, San Diego County Fair Chance Ordinance, and the California Fair Chance Act, where applicable, arrest or conviction records will be considered for Employment in accordance with these laws. At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship to responsibilities such as accessing sensitive company or customer information, handling proprietary assets, or collaborating closely with team members. We evaluate these factors thoughtfully to establish a secure and trusted workplace for all. Applications will be accepted until the position is filled or the posting is removed, unless otherwise set forth on the following webpage. Please visit this link for information about anticipated application deadlines: https://pwc.to/us-application-deadlines The salary range for this position is: $99,000 - $232,000. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. All hired individuals are eligible for an annual discretionary bonus. PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation, personal and family sick leave, and more. To view our benefits at a glance, please visit the following link: https://pwc.to/benefits-at-a-glance

Posted 2 weeks ago

PwC logo
PwCSan Antonio, TX
Industry/Sector Not Applicable Specialism Managed Services Management Level Manager Job Description & Summary At PwC, our people in risk and compliance focus on maintaining regulatory compliance and managing risks for clients, providing advice, and solutions. They help organisations navigate complex regulatory landscapes and enhance their internal controls to mitigate risks effectively. As a risk management generalist at PwC, you will provide advisory and practical support to teams across a wide range of specialist risk and compliance areas. Enhancing your leadership style, you motivate, develop and inspire others to deliver quality. You are responsible for coaching, leveraging team member's unique strengths, and managing performance to deliver on client expectations. With your growing knowledge of how business works, you play an important role in identifying opportunities that contribute to the success of our Firm. You are expected to lead with integrity and authenticity, articulating our purpose and values in a meaningful way. You embrace technology and innovation to enhance your delivery and encourage others to do the same. Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to: Analyse and identify the linkages and interactions between the component parts of an entire system. Take ownership of projects, ensuring their successful planning, budgeting, execution, and completion. Partner with team leadership to ensure collective ownership of quality, timelines, and deliverables. Develop skills outside your comfort zone, and encourage others to do the same. Effectively mentor others. Use the review of work as an opportunity to deepen the expertise of team members. Address conflicts or issues, engaging in difficult conversations with clients, team members and other stakeholders, escalating where appropriate. Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements. Minimum Degree Required Bachelor's Degree Minimum Year(s) of Experience 5 year(s) Demonstrates extensive knowledge and/or a proven record of success in the following areas: Quickly and agilely learn client HCP and HCO engagement processes and ways of working, analyzing for opportunities to optimize, develop, update, and govern team playbooks, SOPs, and process documentation to ensure operational consistency and compliance; Develop and maintain training plans for both new and existing team members; Designing and delivering training curricula for new hires and ongoing development for existing team members; Keeping training materials current with process changes, client requirements, and industry/regulatory updates; Managing and delivering structured onboarding programs for new hires to ensure smooth integration and readiness; Providing coaching and skills development opportunities to build functional expertise across the team; Partnering with leadership to identify training gaps and address them proactively; Designing and executing quality monitoring frameworks to evaluate managed services team delivery accuracy, compliance, and timeliness of deliverables; Conducting regular quality reviews of outputs (e.g., tiering assessments, contracting, payment processing); Tracking and reporting quality performance metrics; identify root causes of recurring errors and define corrective actions; Partnering with leadership to implement corrective training and process refinements; Leading process improvement and optimization; Serving as a key SME in continuous improvement initiatives, contributing to best practices across global operations; Mentoring junior team members; Supporting the process design and implementation of new client or new markets ensuring a high-level of customer engagement, quality, timeliness, and service-readiness across all regions; Managing deliverables on or ahead of deadlines and reporting any issues/risks beforehand; Experience in life science meetings & events, pharmaceutical device or healthcare setting working with HCPs, HCOs or Patients; Identifying opportunities for efficiency, automation, and standardization within the managed services delivery model; Working closely with the client-dedicated operations team to streamline processes while maintaining quality and compliance; Communicating with senior leadership and senior client stakeholders; Delivering "white glove" customer service; Ability to work in a fast-paced environment, with a strong emphasis on quality and accuracy; Monitoring and managing other responsibilities not necessarily listed but logically inherent to the role; Leading teams of individuals with a positive attitude; Strong English language reading comprehension and writing skills. Travel Requirements Up to 40% Job Posting End Date Learn more about how we work: https://pwc.to/how-we-work PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy . As PwC is an equal opportunity employer, all qualified applicants will receive consideration for employment at PwC without regard to race; color; religion; national origin; sex (including pregnancy, sexual orientation, and gender identity); age; disability; genetic information (including family medical history); veteran, marital, or citizenship status; or, any other status protected by law. For only those qualified applicants that are impacted by the Los Angeles County Fair Chance Ordinance for Employers, the Los Angeles' Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, San Diego County Fair Chance Ordinance, and the California Fair Chance Act, where applicable, arrest or conviction records will be considered for Employment in accordance with these laws. At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship to responsibilities such as accessing sensitive company or customer information, handling proprietary assets, or collaborating closely with team members. We evaluate these factors thoughtfully to establish a secure and trusted workplace for all. Applications will be accepted until the position is filled or the posting is removed, unless otherwise set forth on the following webpage. Please visit this link for information about anticipated application deadlines: https://pwc.to/us-application-deadlines The salary range for this position is: $99,000 - $232,000. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. All hired individuals are eligible for an annual discretionary bonus. PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation, personal and family sick leave, and more. To view our benefits at a glance, please visit the following link: https://pwc.to/benefits-at-a-glance

Posted 2 weeks ago

Arthrex, Inc. logo

QA Specialist II - Sterilization

Arthrex, Inc.Ave Maria, FL

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Job Description

Requisition ID: 64180 Title: QA Specialist II - Sterilization Division: Arthrex Manufacturing Inc (US02) Location: Ave Maria, FL

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a QA Specialist II, Sterilization for our manufacturing site in Ave Maria, FL. The QA Specialist II maintains Arthrex Manufacturing Inc (AMI) Sterilization Facility's quality assurance program in accordance with Quality Systems Requirements. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better.

Duties and Responsibilities:

  • Ensure proper and timely accurate completion of sterile load files of AMI products;
  • Maintain the Sterile Release program for loads produced by AMI and ensure timely and safe product release to meet customer requests;
  • Report and act by opening, disposition, evaluating, and closing on Non Conformances observed during sterilization processes for AMI to provide a resolution for the disposition of affected loads;
  • Support the AMI Sterilization Facility Personnel to investigate Non Conformances related to sterilization processes in order to determine the root cause and prevent re-occurring issues;
  • Support the AMI Sterilization Facility program to identify and encourage process improvement;
  • Maintain procedures related to the Quality Assurance - Sterilization department activities and review procedures / records related to the AMI Sterilization Facility processes;
  • Function as lead auditor and/or subject matter expert for quality management system audits of
  • Arthrex's sterilization service providers in accordance with applicable standards, e.g., ISO 13485, ISO 11135, ISO 11137 parts 1 and 2, and international regulatory directives;
  • Generate and execute protocols for sterilization processes (i.e. EO, Gamma, X-Ray etc.) and equipment validation and re-validations, along with reports and conclusions;
  • Manage all activities related to sterilization validations and/or testing, and directly interact with external and corporate laboratories, and sterilizers personnel to accomplish the assigned tasks;
  • Assess devices for compatibility to proper sterilization modalities, e.g., radiation and ethylene oxide, by validating and/or adopting Arthrex manufactured products to established or new families using microbiological and sterilization theory and practice according to applicable ISO requirements;
  • Effectively work within a cross functional team environment as both a champion and team member;
  • Support Arthrex business and expansion goals;
  • Must be able to travel domestically and internationally up to 10% of the time

Education and Experience:

  • BS in STEM discipline
  • 2+ years relevant experience

Skills and Knowledge:

  • Knowledgeable of FDA and ISO guidelines for the sterilization modalities of medical devices required.
  • Manufacturing process knowledge preferred.
  • Project management and communication skills training preferred.
  • Working knowledge of sterilization test systems requirements.
  • Hands on experience managing sterilization product assessments and validations.
  • Test protocol and report writing experience.
  • Knowledge of ISO 13485 guidelines and principles of quality requirements
  • Experience with CAPA processes and non-conformance investigation techniques to determine root-cause
  • Knowledge and Skill Requirements/Specialized Courses and/or Training:
  • Experience in project management, risk management (such as FMEA, FTA, FMECA) tools are highly desirable. Experience in working in Medical Device industry, CAPA, Complaint Management, and Nonconformance Reporting required.

Machine, Tools, and/or Equipment Skills:

Proficiency in the use of Personal Computers and computer programs, particularly the Microsoft Office Suite; Excel, Word, PowerPoint (or equivalents if changed by the Company). SAP and / or Pilgrim Quality Data experience desirable.

Reasoning Ability:

Ability to identify opportunities, collect data, analyze established facts, draw valid conclusions, and implement change. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

Mathematical Skills

Ability to comprehend and apply mathematical principles to the degree required to perform the job based upon job requirements.

Language and Communication Skills:

Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures.

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required sit; use hands and fingers, to handle, or feel; and reach with hands and arms. The employee must occasionally lift and/or move up to 20 pounds.

Arthrex Benefits

  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Free Onsite Medical Clinics
  • Free Onsite Lunch
  • Tuition Reimbursement Program
  • Trip of a Lifetime
  • Paid Parental Leave
  • Paid Time Off
  • Volunteer PTO
  • Employee Assistance Provider (EAP)

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.

Making People Better at Arthrex

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Job Details

Date: Dec 7, 2025

Requisition ID: 64180

Salary Range:

Job title: QA Specialist II - Sterilization

Arthrex

Location:

Ave Maria, FL, US, 34142

Nearest Major Market: Naples

Job Segment: QA, Quality Assurance, Medical Device, Orthopedic, Business Process, Technology, Quality, Healthcare, Management

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