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QA Automation Team Lead Pay from $121,000 to $150,000 per year Corporate Headquarters 12575 Uline Drive, Pleasant Prairie, WI 53158 Drive quality and innovation as Uline’s Quality Assurance Automation Team Lead. Guide and support your team to implement automated testing solutions and deliver top-tier applications for our growing company! Careers Packed with Potential. Backed by 45+ years of success, Uline offers opportunities to grow your career with stability you can count on. Position Responsibilities Manage a team of QA analysts, fostering strong collaboration and driving high performance. Represent Test Automation to QA and IT leadership, ensuring alignment with organizational goals. Prioritize and assign QA work and assignments. Balance strategic oversight with hands-on testing to ensure quality and efficiency. Implement best practices, policies and procedures to optimize QA processes. Track and report quality metrics, ensuring continuous improvement and accountability. Minimum Requirements Bachelor's Degree in Information Technology, Computer Science or a related field. 8+ years of experience in QA automation, with 3+ years in a leadership or mentoring capacity. Strong expertise in automated test frameworks such as Playwright, Cypress, Selenium, REST-assured, etc. Experience programming with a modern language such as JavaScript, Typescript or Python. Strong understanding of SQL, API testing and Agile. Benefits Complete health insurance coverage and 401(k) with 6% employer match that starts day one ! Multiple bonus programs. Paid holidays and generous paid time off. Tuition Assistance Program that covers professional continuing education. Employee Perks On-site café and first-class fitness center with complimentary personal trainers. Over four miles of beautifully maintained walking trails. About Uline Uline, a family-owned company, is North America’s leading distributor of shipping, industrial, and packaging materials with over 9,000 employees across 14 locations. Uline is a drug-free workplace . All positions are on-site. EEO/AA Employer/Vet/Disabled #LI-MT1 #CORP (#IN-PPITL1) Our employees make the difference and we are committed to offering exceptional benefits and perks! Explore Uline.jobs to learn more!

Job Description Responsibilities: Responsible for organizing, reviewing, and maintaining quality assurance (QA) documentation across departments. Ensure documentation is accurate, complete, and aligned with company policies and regulatory requirements. Support audits, inspections, and compliance reviews by retrieving and preparing necessary documents. Assist with the creation, revision, and tracking of standard operating procedures (SOPs), work instructions, and QA forms. Work closely with warehouse, maintenance, and operations teams to ensure proper recordkeeping and traceability. Job Functions: Display strong work ethic and honesty; adhere to all company guidelines, policies, and procedures. Engage work with a high sense of urgency; be highly organized and detail-oriented. Maintain confidentiality of sensitive documentation and proprietary company information. Ensure proper version control, document filing, and archiving of QA-related records. Assist with internal audits and quality investigations by pulling relevant documentation. Follow up on missing or incomplete documentation from internal departments. Support training documentation and maintain up-to-date logs as required. Additional job duties can be added at any time. Desired Knowledge, Skills, and Experience: Strong attention to detail and ability to work with precision and consistency. Familiarity with quality management systems or document control processes is a plus. Basic understanding of manufacturing, warehouse, or industrial operations is preferred. Proficient in Microsoft Office (Word, Excel, Outlook); experience with shared drives or document control software is a plus. Minimum Education Required: High School Diploma or equivalent . Minimum Experience Required: 1–2 years QA support experience . Ability to read and write in English and understand basic math. Excellent verbal and written communication skills. Physical Requirements: Primarily desk-based but may require occasional walking through warehouse or plant areas. Ability to sit or stand for extended periods. Must be able to lift up to 25 lbs occasionally (e.g., moving file boxes or binders). Job Type: Full-time Equal Opportunity Employer IND1

Description Craft and Technical Solutions is an established Marine and Industrial Staffing Company with offices all over the country. We partner with businesses as well as jobseekers to place individuals into positions efficiently. We are currently in need of QA/QC Inspectors to join our team in San Diego, CA! Pay Rate: $24/hour Job Details: Perform basic inspection of shipbuilding and ship repair work in accordance with established policies to ensure compliance with technical requirements Performs other Quality Assurance tasks as assigned by supervisor/manager Ensure correct materials and proper fabrication and installation procedures are utilized during production processes Evaluate results from tests and inspections to determine acceptability with assistance as needed Basic understanding and ability to research technical documents including engineering drawings, specifications, standards, test procedures, work instructions, NAVSEA Standard Items, and contract requirements Basic understanding of the usage of calibrated equipment and ability to validate calibration of equipment, gauges, and tools used in production and inspection in accordance with established policies Basic ability to recognize and document nonconformance’s per company policy Basic understanding of root cause analysis, corrective action, and preventative action practices Ability to learn and perform process audits and surveillances Drafts, reviews, and/or submits QA reports and technical documents Actively participates in implementing and monitoring continuous improvement initiatives to improve safety, improve quality, reduce cycle time, and reduce costs Brings complex issues to the attention of Supervision Requirements High School education or equivalent; Additional technical education or college education a plus Zero to four (0 – 4) years of Quality Assurance or related experience Knowledge of shipbuilding and repair operations a plus Ability to develop technical knowledge of ship construction and repair processes including welding, structural, machinery, electrical piping, ventilation, flushing and develop familiarity with various measuring instruments related to inspections. Computer literate; knowledge of Microsoft Word, Excel, Outlook, PowerPoint, and IFS Quality Modules a plus Good written and verbal communication skills, integrity, presentation skills, problem solving skills Positive attitude and determination to help others required Able to learn to read and understand blueprints, standard/specifications, regulatory body requirements, and ship specifications Must be a team player Benefits CTS, LLC offers a comprehensive benefit packet to eligible employees. Eligible employees may enroll in: Health Dental Vision Voluntary Life/Voluntary AD&D Short-Term Disability Long-Term Disability Hospital Indemnity Accident Critical Illness 401k Safety and responsible work practices are of paramount importance at CTS and are woven into the fabric of everything we do. We are committed to employee safety & development, the protection of the environment and the communities where we operate. We are ready to be a partner in your career success! Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform essential job functions. Craft and Technical Solutions, LLC has a consistent policy that requires an online application to be completed before we can further consider you as an applicant for this position. CTS is an EOE AA M/F/Vet/Disability

Position: QA Tech 2 (Post-Harvest, Temp) Department: Agriculture Operations Reports To: Sr. Manager, Field Food Safety Salary Type: Hourly, Non-exempt Salary: $22.00 an hour Location: Salinas, CA Groupe Bonduelle is a company that is making a positive impact Groupe Bonduelle is the world leader in ready-to-use plant-rich food. By joining our company you will have an opportunity to make a positive and sustainable impact on yourself, others and the planet. You will play an active part in our mission to inspire the transition toward a plant-rich diet to contribute to people's well-being and planet health. Groupe Bonduelle Fresh Americas is the U.S. business unit of France based Groupe Bonduelle ( BON.PA ). We are the first business unit of Groupe Bonduelle to become a Certified B Corporation. We operate three processing facilities throughout the U.S. and employ nearly 3,000 Associates who focus on producing and bringing to market fresh vegetable products, prepared salads and plant-rich meal solutions. Groupe Bonduelle is a 170 year old French family-owned company that has been at the forefront of plant based food innovations since 1853. Our ready-to-use plant-rich food products are grown on 168,000 acres by our grower partners and marketed in nearly 100 countries. The company currently employees more than 11,000 Associates globally. Position Summary: This role is a key QA role within our Agriculture Operations and supports QA team leads as they ensure compliance with food safety and quality requirements by fully embracing the Company’s RCE philosophy. This position is exposed to multiple refrigerated areas. And support to inspect all inbound raw produce loads at cooling facilities. The candidate in this position must be self-motivated, problem solver with excellent communication skills and strong intrapersonal skills. Must be able to work unsupervised. What you will Do : Raw product inspection Sampling raw product for inspection Conduct checks Oxygen levels in sealed bins of C&C Iceberg lettuce and Trim Romaine Conduct temperature checks of raw product as necessary Conduct color ration evaluation of Raw romaine Enter results of evaluation into “Paperless” data system Completion of Supplier Notification forms Complete daily inspection reports into Ready BFA data Management System (Paperless) Communicate with Ready Pac field personnel on raw quality issues Communicate with Ready Pac processing facilities on raw quality issues Communicate with raw suppliers on quality issues related to inspection at the cooler Communicate with cooler personnel on raw inspection or cooling process issues. Issue daily inspection report to all RP processing facilities. Follow BFA food safety, and safety policies as applicable to the cooler operation. Conduct other duties related to raw quality, as assigned by the department manager. Minimum Qualifications: Post Harvest inspection experience is desired. Good computer skills (familiar with Microsoft Excel, Microsoft Access, Microsoft Word, Paperless). Good written and oral skills Familiar with Fresh Cut processing Familiar with USDA inspection standards Familiar with raw inspection procedures Bilingual (English/Spanish) is desired. Must be able to work in cold environment Must be able to lift 50 lbs. Must be able to work in a high pace environment Ability to work independently, unsupervised and in a team environment. Must be able to monitor product/process to identify and address any non-compliance Physical Work Environment / Demands : While performing the duties of this job, the associate will be required to perform repetitive movements (i.e., scooping condiments into salad bowls). The associate regularly works near moving mechanical parts and is regularly exposed to extreme cold. The noise level in the work environment is usually loud. Ability to sit or stand for extended periods. Ability to move about within a fast-paced environment in/outside facility, and traverse between the maintenance shop & production floor. Ability to position self to stoop, kneel, crouch, or crawl Ability to frequently move, push, or carry items up to 50lbs Exposed to a cold & wet environment of 34 degrees. Ability to work in outdoor weather conditions Must be able to exchange accurate information through frequent communications within all levels of the organization Must be able to detect, identify, inspect, observe, and assess surroundings Bonduelle Fresh Americas does not require employees to be COVID-19 vaccinated and/or boostered at this time, but does require disclosure of vaccination status and supporting documents. Bonduelle Fresh Americas reserves the right to modify any internal policies, including safety policies, as needed and in compliance with all applicable laws. Bonduelle Fresh Americas is proud to be an Equal Opportunity Employer. We believe in hiring individuals from diverse backgrounds and experiences to create a workforce that truly reflects our communities. All applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other legally protected status. We are committed to providing reasonable accommodation to veterans and individuals with disabilities or special needs during the application process and employment. If you need assistance, please contact us at 626-856-8686 or bfa-info@bonduelle.com .

Description Title: Director, Business Development – Software QA Location: Remote Department: Business Development, Automotive Software Quality Assurance Contract: Full-Time, Permanent Start: ASAP About Side Side (formerly PTW) is a global video game development and services provider, offering technical and creative solutions to many of the largest developers and studios around the world. Founded in 2009 and drawing on 30+ years' experience from our parent company in Japan, Side has since grown to become a global force with 20 studios in 14 countries across North America, Europe, South America, and Asia. Our industry-leading services include game development, art production, audio production, quality assurance, localization, localization QA, player support, community management, and datasets. Help us bring stories to the world! Join a global team of passionate gamers and contribute to delivering unforgettable game experiences. Experience our side of life. For more information, visit www.side.inc. Overview We are looking for a Director of Business Development to drive new business sales for our software quality assurance services in the automotive industry . This individual must be a consultative and highly motivated sales leader , with a proven ability to build long-term relationships with automotive manufacturers, suppliers, and software developers . The ideal candidate will present our QA solutions , liaise with internal operations, negotiate contracts, and manage client relationships. Additionally, this role involves leading a small global team of Business Development Managers to drive revenue growth, cross-sell services, and strengthen client relationships. The successful candidate will be strategic, highly organized , and possess a strong understanding of software QA processes, industry regulations, and automotive software development lifecycle . This position is perfect for an engaging, enthusiastic, and results-driven individual with a passion for software quality and automotive innovation . Growth will be driven through relationship-building, consultative selling, and surpassing revenue targets . The ideal candidate will excel at identifying business opportunities, developing sales strategies, and mentoring a high-performing team . What You’ll Be Doing Driving new business sales to meet individual and team revenue targets Motivating and leading a global new business team to exceed performance goals Identifying and engaging automotive manufacturers, suppliers, and automotive software development firms Attending client meetings, trade shows, and industry events to establish presence and generate opportunities Presenting our QA services in response to client briefs and business needs Developing tailored software QA solutions that align with industry standards and client requirements Collaborating with delivery teams and support functions to optimize engagement time with clients Managing, mentoring, and coaching the business development team Requirements Qualifications Bachelor's degree in Business, Marketing, Engineering, or a related field. Proven experience in business development, sales, or a related role within the automotive or software industry. Minimum of 5-7 years of experience in business development or sales, with at least 2 years in a leadership role Strong understanding of software quality assurance processes and industry regulations. Excellent communication, negotiation, and presentation skills. Demonstrated ability to build and maintain long-term client relationships. Experience leading and managing a global team. Strategic thinker with strong organizational and problem-solving skills. Ability to travel as needed to meet with clients and attend industry events. Benefits What’s in it for you? Competitive Base salary Medical, Dental, Vision, 401k with company matching

Work Schedule First Shift (Days) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description POSITION SUMMARY In this position, you’ll drive quality execution across the sterile operations including manufacturing, filling, packaging and inspection, and associated non batch specific activities in for both commercial and product development services products. Additionally, this position will provide quality guidance and expertise for implementation of practical process improvements and continuous improvement initiatives. Key Responsibilities: Perform daily quality assessments of facility, personnel, and documentation both classified and non-classified areas to uncover errors or deficiencies, assure quality, and compliance per site procedures and cGMPs. Daily interaction with employees to assist with troubleshooting, documentation corrections/notes, and guidance with aseptic technique Champions quality culture by aiding personnel in understanding application of policies and controls Participates in RAPID event response and provides quality guidance for deviation events Advances deviation events to the appropriate area and quality management Performs quality review and approval of procedures, training documents, and forms of moderate to high complexity Performs quality review and approval of deviation and change control of moderate to high complexity Participates as the quality assurance representative in Root Cause Analysis to support deviation investigations of moderate to high complexity Performs quality batch record review Aids in identification of continuous improvement opportunities; Participates in practical process improvement initiatives Qualifications: Bachelor’s degree required, preferably in technology, engineering or microbiology related field. 4+ years of experience with previous experience in Quality Assurance or Quality control or Operations/Manufacturing Equivalent combinations of education, training, and relevant work experience may be considered Previous experience in pharmaceutical industry; preferably aseptic or steriles processes strongly preferred, experience in other regulated environments may be considered (i.e. ISO 9001) Effective time management and prioritization skills. Good interpersonal skills to establish and maintain effective working relationships with employees and the public, including tact to handle sensitive matters. Good verbal and written communication skills (legible handwriting). Good Presentation Skills. Demonstration of active listening skills. Ability to troubleshoot process and equipment issues Self-driven, demonstrated ownership & responsibility Ability to lead, support & motivate a team Ability to learn Technical Writing experience Professional certifications (ex: CQA) and training (Six Sigma) is a PLUS Ability to develop solutions that are mutually beneficial to the client and to Thermo Fisher. Ability to function independently and as part of a team. Demonstrated Commitment to our fundamental principles of Integrity, Respect, and excellence. Understanding of the Quality systems and investigation documentation Ability to adapt to a changing environment quickly and easily Ability to respond disciplined and rationally under pressure Ability to display command authority and remain firm in complex situations Physical Requirements: Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations. Ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time Manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds. Arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time. Visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time. Ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Safety glasses, safety shoes, lab coat, nitrile or similar gloves, safety apron, organic respirator occasionally. BENEFITS We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! http://jobs.thermofisher.com Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/disability access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process. This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

QA Lead (Automation) Furntiure.com – Atlanta, Ga WHO WE ARE Furniture.com is building the most intelligent furniture shopping platform on the planet. We don’t sell furniture. We help people find it better. We are a technology company in the service of furniture. A creative industry, with a consumer base that really cares about the decisions they make. With over 2 million products from 60+ trusted brands, our AI-powered search platform connects shoppers with the right pieces—based on style, space, budget, and intent —without the 15-tab madness of traditional furniture search, discovery and shopping. ABOUT THE ROLE Furniture.com is a high growth startup backed by one of America’s top furniture retailers. We are looking for a QA leader who is technical and possesses deep experience with software delivery and test automation frameworks. This is a technical leadership role where you will provide guidance to automation and manual testers while establishing QA protocols demonstrating a bias towards automation. This role collaborates closely with Software and Data Engineers, Product Managers, and Designers to develop a world class user experience for our customers. This role requires coding on a regular basis. WHAT YOU’LL DO Technical Execution Build and manage testing frameworks for functional, system integration, and regression testing. Develop and execute automated test cases using commercial or open-source frameworks Collaborate with QA engineers to determine the best test and automation frameworks for web, API, and microservice testing Build and manage testing frameworks, test case documentation to facilitate functional, system integration, and regression testing Develop frameworks and automated test cases commercial or open-source frameworks Able to develop manual and automated testing strategies for existing systems Contribute designs and code for test automation workflows Champion adoption of AI tools to boost automation code and testing efficiencies. Collaboration Partner with software engineers, product managers, and designers to ensure a world-class user experience Participate in Agile Scrum ceremonies, including Sprint Planning, Demos, and Backlog Refinement Collaborate with other software an QA engineers to determine the appropriate test and automation frameworks for web, API, and microservice testing Participate in Agile Scrum ceremonies like Sprint Planning, Demos, Estimation, Backlog Refinement etc. Participate in architecture design sessions for new features Team Leadership Oversee test case execution, analyze results, and report on test coverage and defect metrics. Mentor and provide guidance to both manual and automation testers Create documentation and training plans for continuous learning for QA team members Oversee the execution of test cases, analyze test results, and report on test coverage and defect metrics Perform reviews, capture metrics to determine opportunities to eliminate churn in releases Will have oversight on all QA operations in multiple pods across software and data engineering teams Innovation with AI Openness to experiment with and evaluate emerging AI tools, providing feedback and sharing insights with engineering team. Ability to balance AI-assisted productivity with deep understanding and manual craftsmanship when necessary. Strong awareness of the limitations and ethical considerations of AI using in software development, especially regarding data privacy and code originality. WHO YOU ARE Bachelor’s degree in Information Technology, Computer Science, or related field 8+ years of test automation experience Experience working with RDBMS and NoSQL databases Experience creating automation for frontend, microservices, and APIs Strong knowledge of Agile testing methodologies and best practices Software Development Life Cycle (SDLC) principles in Agile environments Familiarity with the entire software development life cycle and test cycles (Unit, Regression, Functional, Systems, Performance and Volume, User Acceptance). Experience with testing tools like Cypress, Selenium, BrowserStack, Postman, ReadyAPI etc. Cypress is preferred. Experience testing with 3rd party data integrations (ETL) is a plus Excellent written and verbal communication skills Must be able to code in one or more programming languages Python, JavaScript, TypeScript etc. AWS cloud experience is essential but will consider candidates with Azure or GCP Working knowledge of CI/CD frameworks. GitHub Actions is preferred Familiarity with modern AI-assisted development tools (e.g., GitHub, Copilot, Cursor, or ChatGPT) to accelerate code generation, documentation and refactoring. Experience using AI-powered debugging and testing tools to identify and resolve issues faster. Comfortable with prompt engineering practices to fine-tune interactions with AI assistants and agents to enhance the product and team efficiency. The company is an equal opportunity employer. We do not discriminate in hiring or employment against any individual based on race, color, gender, national origin, ancestry, religion, physical or mental disability, age, veteran status, sexual orientation, gender identity or expression, marital status, pregnancy, citizenship, or any other factor protected by anti-discrimination laws Applicants must be authorized to work in the U.S.

JOB SUMMARY This position is responsible for the compliance review of Biopharmaceutical Development GMP data. This includes the review and approval of release, in- process, and stability test data. This position is also responsible for the review and approval of method qualifications and validations. Another responsibility is the review and approval of laboratory investigations and deviations associated with the biopharmaceutical development department. JOB RESPONSIBILITIES: Performs compliance review on the following records: release, in-process, and stability data. Responsible for the review and approval of method qualifications and validations Responsible for the review and approval of deviations and laboratory investigations. MINIMUM REQUIREMENTS: BS and 11+ years experience or MS and 8+ years experience in a CGMP regulated environment within biopharmaceuticals or equivalent. Experience in QA review of analytical data (release, in-process, and stability), experience in reviewing method qualifications/validations and the review and approval of laboratory investigations and deviations. Knowledge of USP, EU and JP cGMP guidelines. Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Basic math skills are required. Ability to apply concepts of basic algebra and statistics. Be able to sit for long periods of time. Ability to lift 20 pounds. Ability to use w ord processing, database, spreadsheets, power point, internet, e-mail, calendar, c omputer, telephone KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization. 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.

Decima International is a professional services company, providing project management and controls services to clients in the United States and the Middle East. Our mission is to become the premier professional services provider across all industry sectors we are engaged in. To accomplish this, Decima International’s founders established a simple yet powerful formula: Approach each client engagement as a partnership , create an environment that attracts the most talented professionals and allows them to flourish, and regulate growth to maintain excellence in our service standards. Decima International is a professional services company, providing project management and controls services to clients in the United States and the Middle East. Our mission is to become the premier professional services provider across all industry sectors we are engaged in. To accomplish this, Decima International’s founders established a simple yet powerful formula: Approach each client engagement as a partnership , create an environment that attracts the most talented professionals and allows them to flourish, and regulate growth to maintain excellence in our service standards. If you are interested in a long and rewarding career working with high-profile clients on some of the most challenging projects in the world, then Decima is where you belong. At Decima, you will be able to explore incredible growth and professional development opportunities. We are looking for a driven and capable Electrical QA Manager to support the development of multiple hyperscale data center projects for one of our top technology clients. This is a client-facing role that requires strong interpersonal, communication, and organizational skills; the ability to self-direct; effective client representation; and a strong foundation in project management fundamentals. The ideal candidate must be able to manage multiple projects concurrently. A strong background in data center development, design, engineering, controls, and operational requirements is a significant plus. You will play an integral role in developing and implementing the Quality Management System (QMS), as well as coordinating, performing, and completing all construction audits and commissioning services related to the project. The Electrical QA Manager is accountable for the quality of work performed, compliance with building codes and safety regulations, and for meeting the project’s contractual requirements as set forth by the client. We’re seeking dedicated individuals with a passion for innovation and the ability to multitask in a fast-paced environment. We will help you grow, pursue, and fulfill what inspires you, so we can make big impacts on the world, together. RESPONSIBILITIES Understand project scope and requirements Ensure compliance with quality standards, building codes, safety regulations, and environmental guidelines Review and verify material submittals for A/E and client approval Confirm that delivered materials match approved submittals Manage and review submittals, RFI logs, maintenance logs, and other project documentation in a timely manner Update QC punch lists and coordinate with general contractors (GCs) and subcontractors for completion Conduct internal quality audits and on-site inspections Adhere to Quality, Health, Safety & Environment (HSE) standards Provide technical support to address operational challenges and client concerns Plan and inspect Definable Features of Work (DFWs) Develop and implement audit and test plans for quality inspections and testing Maintain and update quality manuals, checklists, and forms Collaborate with third-party QA/QC firms as needed Participate in Quality Management System (QMS) audits Build and maintain relationships with project partners, consulting engineering firms, public agencies, and clients Ensure document control compliance and maintain project submittal logs and quality control reports Verify and document material compliance with approved submittals Compile and submit project closeout documents, including O&M manuals, as-builts, and warranties Investigate and resolve non-conformance issues promptly Ensure timely calibration of inspection, measurement, and test equipment Liaise with the General Contractor, Client, and Project Management team to resolve quality issues Prepare and present reports on progress, findings, and recommendations to management Review subcontractor submittals for compliance Coordinate and monitor subcontractors, suppliers, direct labor, and materials Collaborate with utility suppliers for final service connections Coordinate activities with inspection agencies Complete required MEPS and electromechanical inspections Assist in preparing periodic QA/inspection progress reports Review and approve subcontractor work completion percentages Oversee commissioning processes Manage MEP project closeout to ensure all requirements are met QUALIFICATIONS Required Qualifications: 12+ years of construction and quality management experience Bachelor’s degree in Electrical Engineering, Mechanical Engineering, or a related field Prior experience with hyperscale data center development and construction Experience managing field engineering, inspection, and NDE for QA/QC functions Proficient in reading and interpreting plans, specifications, drawings, contracts, and documents related to MEP scopes Ability to develop and manage non-conformance and defect tracking programs, including root cause analysis Deep understanding of codes, standards, job specifications, project procedures, and applicable regulations Ability to thrive in high-production environments and under tight deadlines Strong technical knowledge of materials and construction practices Experience as an Electrical QA/QC Supervisor for large commercial, industrial, or mission-critical construction projects Excellent knowledge of construction Quality Management Systems (QMS) Familiarity with punch list and project closeout procedures Excellent attention to detail and strong analytical skills In-depth knowledge of high-, medium-, and low-voltage systems, HVAC, control systems, commissioning, LEED/green building standards, and general ground-up construction as they relate to MEPS Preferred Qualifications: Project Management Professional (PMP) certification Construction Quality Manager Certification (CQMC) U.S. Army Corps of Engineers (USACE) QA experience Certified Quality Auditor (CQA) Member of the American Society for Quality (ASQ) Six Sigma certification ISO 9001 experience Green Business Certification (LEED) POSITION DETAILS Location (On-site): Indianapolis, Indiana Position: Electrical QA Manager Classification: Salary-based, full-time, regular hours Current U.S. work permit required. This position does not offer employment sponsorship (e.g., H-1B visa sponsorship or transfer is not offered). PRODUCTIVITY TOOLS Microsoft Office Microsoft 365 CxAlloy Job Type: Full-time Schedule: 8-hour shift Work Location: (On-site) Indianapolis, Indiana Decima International is an Equal Opportunity Employer who is committed to the safety and wellbeing of all. All qualified applicants will receive consideration for employment without regard to race, religion, creed, color, national origin, ancestry, sex (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, medical condition, marital or domestic partner status, sexual orientation, gender, gender identity, gender expression and transgender status, mental disability or physical disability, genetic information, military or veteran status, citizenship, low-income status or any other status or characteristic protected by applicable law. At Decima International, we offer a competitive salary package, including paid time off and performance-based bonuses. We also provide excellent medical, vision and dental insurance for our employees.

6-10 yrs. Software Development Lifecycle experience 6-10 yrs. MS Office/PowerPoint experience Experience communicating effectively in a professional setting both written and verbally (including presentations) Bachelor’s degree in IT or related field or equivalent experience Overall QA Experience Overall Training Experience Requirements gathering and documentation Scrum Product Owner Accredited Certification International Institute SAFe Scrum Master 5.0 Scaled Agile Experience acting as Scrum Master Experience acting as QA lead or Manger Tableau Server Administration and Report Development experience PL/SQL Work remote temporarily due to COVID-19. Compensation: $42.00 - $52.00 per hour About Us AHU Technologies INC. is an IT consulting and permanent staffing firm that meets and exceeds the evolving IT service needs of leading corporations within the United States. We have been providing IT solutions to customers from different industry sectors, helping them control costs and release internal resources to focus on strategic issues. AHU Technologies INC. was co-founded by visionary young techno-commercial entrepreneurs who remain as our principal consultants. Maintaining working relationships with a cadre of other highly skilled independent consultants, we have a growing number of resources available for development projects. We are currently working on Various projects such as media entertainment, ERP Solutions, data warehousing, Web Applications, Telecommunications and medical to our clients all over the world.

Quality Assurance Inspector Position Summary Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. This 206,878 square-foot facility, located in the Philadelphia area is Catalent’s global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured to hold a single product, or multiple products as determined by study requirements. We offer manual patient kit assembly along with semi-automated and automated wallet sealing and high-speed automated carding to meet the needs of studies of all sizes. For temperature sensitive products and those with minimal to zero allowable time out of environment, we can perform secondary packaging in refrigerated and frozen packaging rooms or over dry ice depending upon your project needs. Using our Clinicopia global labeling system with its multi-lingual label phrase library we can design single panel, booklet labels or our unique Peel-ID™ safe storage labels for your studies. Single panel and Peel-ID™ safe storage labels can be conveniently reviewed and approved online via our Fusion portal before being printed and inspected at our facilities. Catalent Pharma Solutions in Philadelphia is hiring a Quality Assurance Inspector. The Quality Assurance Inspector reports to the Quality Supervisor. The Quality Inspector is responsible for process monitoring and auditing of packaging operations, the duties including real-time batch documentation review, monitoring of adherence to cGMP, training on cGMP where necessary, and supporting actions (if required) for resolution of deviations and investigations. The scope of work will cover packaging room and equipment set up, equipment verification, routine packaging operations, line clearances, room and equipment cleaning activities. The Quality Inspector will identify opportunities to improve the ‘right-first-time’ performance of the operation and will manage those opportunities to implementation and improvement, in partnership with Production personnel. This is a full-time role position: Monday-Friday: 7:45am-4:15pm. Hourly, Onsite Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Role Responsible for ensuring that Standard Operating Procedures are consistently followed, and that cGMP’s are observed, in the course of incoming inspection, distribution, label control, destruction and returns. This may require simultaneous auditing and/or monitoring of one or more processes. This role can support both Commercial and Clinical Operations Verifies and inspects incoming materials and works accordingly with Quality and Project Management to handle any possible discrepancies Perform inspection and release of all clinical and commercial drug products and components received from customer or vendor as per customer specifications protocols and/or Catalent SOPs, includes review of all inventory labels applied to the containers and paperwork generated from JDE with receipt paperwork Perform inspection and release of all shipping and distribution materials to clinical sites or clients by reviewing all associated paperwork and picked material, including verification of each individual randomized container and compliance with customer specific distribution protocols Perform inspection and release of materials slated for destruction, by reviewing the associated paperwork and picked materials. Inspect and release of clinical open, randomized, single panel booklet and multi language labels produced by external vendors and Clinical Supply Services by comparison to approved label proof or label copy request Reviews BMS system printouts and chart recorder printouts for out of specification temperatures, humidity and pressures. Inspect retain samples, as required. Maintains & provides departmental metrics. Assists in walk through audits of the Supply Chain facility, Label control room, Refrigerator/Freezer and associated areas to ensure cGMPs and SOPs are being followed Reviews Supply Chain Facility logbooks, Label Room logbooks, Pest Control logbooks and Sampling Room logbooks for GMP compliance and revises SOPs as needed Partners with other departments in resolving unplanned deviations, investigations, in troubleshooting, and in process improvements. Performs additional sampling/testing protocols on clinical trial materials as requested by the customer. Participate in customer audits when required. Complete & maintain documentation Performs other duties or tasks as requested or required by QA Management. All other duties as assigned; The Candidate Requires a Bachelor’s Degree or a minimum of five years of Production/ Quality Assurance experience. Proven track record of monitoring/auditing for quality assurance and/or identifying potential efficiencies in a production environment preferred. Experience in a regulated field preferred – pharma, food, automotive, etc. Good Computer Skills. Knowledge of MS Office and Inventory Management system are a plus. Basic knowledge of Lean Six Sigma methodologies an advantage Good knowledge of the application of FDA cGMP’s. Individual may be required to sit, stand, walk regularly and occasionally lift up to 15 pounds Occasional requirement to work in cold environment to fill orders (walk-in refrigerator/freezer) Why you should join Catalent: Defined career path and annual performance review and feedback process Diverse, inclusive culture Positive working environment focusing on continually improving processes to remain innovative Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 152 hours of PTO + 8 paid holidays Several Employee Resource Groups focusing on D&I Dynamic, fast-paced work environment Community engagement and green initiatives Generous 401K match Medical, dental and vision benefits effective day one of employment Tuition Reimbursement - Let us help you finish your degree or start a new degree! WellHub- program to promote overall physical wellness Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE .

Description At SNS, we build world-class products for teams of video editors and filmmakers. We get our hands dirty with server hardware, software, storage, high speed Ethernet, cloud, AI... we're completely up and down the stack, and we like people who love to build things and aren't afraid to roll up their sleeves. If you started taking things apart and programming before you could drive a car, then you're probably someone who will love working on our team. We're constantly growing, and we're currently looking to expand our team with people who have experience in several of the areas below. If we hire you, you will be thoroughly immersed in designing and developing new products, as well as evolving our existing products—this may take multiple forms including research, architecture, coding, testing, tuning/optimization, documentation, etc. Requirements We don't expect anyone to have all of these things, but you should be the kind of person who gets excited about digging into something you've never done before, and then running with it . Linux product engineering/development (e.g. kernel, embedded, virtualization/VirtualBox, KVM/qemu, Docker, shell scripting) Development experience with C/C++, Python, .NET, Java, React, SQL Networking/storage engineering/development/tuning (e.g. mdadm/lvm2/RAID, Samba, TCP/IP, NAS, file systems like XFS/ZFS, FUSE) Cloud product engineering/development (e.g. SaaS, IaaS, AWS products like S3 and EC2 (or Azure/GCP equivalents), Stripe). Bonus if you've taken an on-prem application and migrated it to a SaaS model. Even more bonus points if you have experience with clustered file systems like Gluster or Ceph storage tuning/performance Strong interest in/embrace of AI tools, with experience applying them to more quickly complete various projects A great sense of humor, and some intense interest in subjects that most people don't understand, because those are characteristics of people who usually fit best on our team Triple bonus points if you also happen to have some experience building video-related software products or with open source software like ffmpeg. Benefits Some of what we offer to you: Competitive pay, work from home PTO Health insurance Matching 401k Weekly pay period A spot on a fantastic team that loves what they do The ability to have your contributions recognized in a big way A spirited, growth-oriented culture that results in an average tenure of 7+ years A human reviews every response we get from this post. We're not going to send you through a bot. You're not going to have to reformat your resume, and we're not going to subject you to any kind of online personality tests. In exchange, we're kindly asking that you send not just your resume, but that you also say hello and include a personal note to let us know who you are and why you think we should interview you. Thanks!

About Knot Knot’s mission is to empower consumers and businesses alike with connected merchant and banking experiences. Knot is like “Plaid for merchant connectivity.” We are building the platform connecting merchants to the many applications that consumers and businesses interact with everyday. Our flagship CardSwitcher product allows consumers to instantly update & manage their cards on file with online merchant accounts (e.g. Netflix or PayPal), while newer products like TransactionLink support the retrieval of item-level transaction data. We are building many new products on top of our novel merchant connectivity platform and we hope you choose to come build them with us! Founded in 2021, Knot was founded by two brothers and Thiel Fellows - Rory and Kieran O’Reilly - and today powers connected online payment experiences for hundreds of thousands of consumers. Companies like American Express, PayPal, Current, BILT, Step, and more choose to embed Knot’s SDK in their apps to power best-in-class experiences for their customers. Knot is proudly backed by a select group of investors, including Nava Ventures, 8VC, American Express, Plaid, and co-founders & CEOs of prominent companies like Twitter, Warby Parker, Allbirds, Casper, Intercom, Deel, Italic, DraftKings, and many more. Working at Knot We’re a world-class team hailing from all over the globe with the vast majority of the company in engineering roles. We are looking to further solidify our presence in NYC to be at the heart of the financial services ecosystem. Our team is relentlessly focused on building for our customers and every member of the financial services ecosystem. We take our work seriously and have fun while doing it. Both are equally important. What you’ll do Use a creative, yet robust approach to design and implement testing strategies for frontend and backend systems (iOS/android/web/backend), including those often difficult to test. Work collaboratively with various engineers and product management to define what “quality” means and chart a path to a higher degree of software quality and reliability. Proactively identify existing and future high risk areas of the software that are prone to breakage and integrate this context into your testing prioritization. Evaluate and integrate new testing tools and methodologies. Build and maintain automated test suites and perform manual testing where applicable. What you’ll need to get the job done 5+ years of QA engineering experience. Strong expertise in automated testing frameworks (we use Jest, Cypress, Pest). Experience testing fullstack applications (we use React/TS, Laravel/PHP, and native SDKs). Knack for writing scripts that significantly improve and aid the testing and quality assurance process. History of leveling up individual and teams of engineers. You excel in a rapidly growing organization and embrace challenging problems, tackling them directly and taking the initiative to lead the solution. Eagerness to work in a fast-paced, dynamic environment and constantly grow & develop your craft. Expert communication and ability to collaborate seamlessly with product teams. Tech React frontend with Styled Components React-query/Axios for API calls PHP/Laravel, Typescript/Node, Python, Go, and Socket.io in the backend CloudSQL & Redis Hosted on Google Cloud Functions and Kubernetes Github, Linear, Slack, Notion What we offer Interesting and challenging work Competitive base salary + generous early employee equity + benefits 100% medical, dental, and vision insurance coverage for you and your dependents (U.S.) Unlimited PTO Parental leave Beautiful NYC office in the heart of Flatiron

Are you looking to make a difference in patients’ lives with a company that values your expertise? Join us in our mission of delivering compassionate healthcare where it matters most–at home. Pinnacle Home Care, Florida’s largest Medicare-certified home health provider, has been delivering high-quality, patient-centered care for over two decades, and we’re looking for a Quality Assurance Nurse to join our award-winning team. Key Responsibilities Perform centralized coding via scanned medical records and clinician documentation via EMR data. Provide home health coding, OASIS, POC, and quality review. Make independent decisions regarding accurate ICD-10-CM coding and OASIS, POC, and quality data assignments. Review records and recommend changes for clinician review and acceptance based on CMS regulation, industry standards, and coding convention as supported by documentation. Review Plan of Care for accuracy and quality and make needed recommendations. Apply knowledge of medical terminology, disease processes, and pharmacology. Assess and review assessments for coding accuracy based on documentation, CMS regulations and coding conventions, OASIS compliance, and Plan of Care quality and accuracy. Maintain minimal productivity number standards daily. Code all assessments using ICD-10-CM (SHP, and Decision Health Coding Pro software) as well as appropriate industry references. Consult Team Lead and/or Director of Quality & Clinical Outcomes and work out difficult codes and coding problems as needed. Participate in continuous learning and education in ICD-10 coding, OASIS, Quality and Plan of Care development as necessary. Monitor regulatory changes and communicate these changes to the Director of Quality & Clinical Outcomes. Meet or exceed minimum auditing and productivity scores for coding quality and compliance. Maintain quality of coding review with a score of 93% or greater on monthly and/or quarterly quality audits. Plan, prioritize, organize, and complete work to meet established objectives. Ensure the efficient and appropriate use of all company financial resources, including but not limited to arrangements for equipment and other necessary items and services needed. Assist with a variety of special projects and other duties as needed. Adhere to federal, state, and agency regulations and policies to maintain confidentiality of patients and agency information per HIPPA requirements. Follow the Code of Conduct policy and submit all documentation in a timely manner according to agency policy. Attend in-service and education as required. Qualifications Current RN license (state-specific). Associates degree or greater in a clinical program. Nationally accredited Coding ICD-10 certification required and maintained yearly. Nationally accredited OASIS certification required and maintained yearly. Formal clinical background. Minimum three years of on-going coding and abstracting experience in ICD-10-CM for home health agencies preferred. Must be proficient in the use of a PC, web-based portals, database software, and Microsoft Office Suite (Access, Excel, Outlook, Power Point and Word). Home health experience preferred. Experience with OASIS analysis preferred. Knowledge of SHP and/or Decision Health Coding Pro preferred. Why Choose Pinnacle? Personalized, One-on-One Care : Help patients heal and regain their independence by delivering individualized care in the comfort of their homes. Growth & Stability : Over two decades as Florida’s largest home health agency. Ongoing Professional Development : Free Continuing Education Units (CEUs) to support licensure and career advancement. Competitive Benefits & Perks : Including Daily Pay (work today, get paid tomorrow!) and an employee referral program where you can earn rewards. Recognized Excellence : Ranked as a USA Today Top Workplace. Flexible Scheduling : Enjoy a schedule that aligns with your personal priorities. Supportive & Fun Culture : Join a collaborative, forward-thinking team that values both professional excellence and personal fulfillment. Pinnacle promotes an inclusive environment and is an equal opportunity employer. We prohibit discrimination or harassment based on race, religion, age, gender, national origin, disability, veteran status, or other legally protected characteristics. Be part of a company that empowers clinicians to make a difference in the lives of over 10,000 patients across Florida every day. Apply now!

This role is responsible for ensuring compliance to quality and food safety requirements and will work directly with QA management. PRIMARY RESPONSIBILITIES: Job is an individual contributor. Job is an individual contributor and has no direct reports. Review QA/HACCP paperwork used in all production departments and fill out correctly. Be able to interact with and communicate with various team members in management, QA, and production as well as government officials, and 3rd party contractors. Perform all QA Tech responsibilities for routine quality checks, and audits on production, the dock, and the facility. Develop and maintain databases as needed. Qualified to perform QA sampling and testing methods Understand of the processes and methods involved in food production. This role has the responsibility to understand and places in practice appropriate safety procedures. This responsibility is achieved through education, training, use of protective equipment (as applicable) and by following safety policies, regulations, standards, and laws. Perform other duties as assigned. WORK ENVIRONMENT: Work is generally performed within a business professional office environment, with standard office equipment or on Production floor. Work conditions are typical of an office & plant environment. Production is a refrigerated environment. This role does not require any domestic travel Required to wear extensive GMP uniforms to include hairnet, gloves, lab coats, and rubber boots. will also be required with no exceptions to wear personal protective equipment such as cut resistant gloves, bump cap, steel mesh gloves. Position requires the physical agility to perform continuous lifting up to 15 pounds, bending, squatting, pushing, pulling, stretching/reaching, use hands or fingers, talk, hear, feel objects, tools, controls and standing/walking on concrete flooring. Position requires the physical ability to stand/walk for the duration of work hours

Benefits: 401(k) 401(k) matching Bonus based on performance Competitive salary Profit sharing Training & development About the Role: We are seeking a passionate and experienced Registered Nurse to join our team at Homewatch CareGivers in both East Cobb in Marietta, GA and Homewatch CareGivers of Canton. As a lead Nurse in our organization, you will play a crucial role in providing high-quality care to our clients and ensuring the success of our nursing staff. Responsibilities: Oversee the home care and clinical care departments and ensure compliance with all healthcare regulations Write Care Plans and do Quarterly QA visits for our clients Conduct regular assessments of client needs and create individualized care plans Conduct regular skills assessments of our caregiver and nursing team Requirements: Active RN license in the state of Georgia Minimum of 1 year of nursing experience, with at least 1 years in a leadership role Strong communication and interpersonal skills Ability to multitask and prioritize in a fast-paced environment Passion for providing compassionate and personalized care Must be able to work independently with little to no oversight About Us: Homewatch CareGivers East Cobb and Canton has been a trusted provider of in-home care for over 4 years. Our dedicated team is committed to enhancing the quality of life for our clients and their families. We offer a supportive and inclusive work environment where employees are valued and empowered to make a difference in the lives of others. Flexible work from home options available. Compensation: $55.00 per hour Homewatch CareGivers of East Cobb/Marietta/Roswell Homewatch CareGivers offers the comprehensive home care services and we believe that exceptional training means a more rewarding experience for you and better care for clients. Homewatch CareGivers is a premier provider of in-home care services for people of all ages, including seniors, children, veterans, the chronically ill, and those recovering from medical procedures. Our care philosophy is based on finding interesting, innovative ways to empower clients and help them feel engaged and respected. We start by making sure our caregivers and office staff are confident and empowered, too. Our Homewatch CareGivers University is a professionally-developed training platform designed to give you the tools and resources you need to make the very most of your time with clients and gain the most satisfaction from your job. It includes online accredited courses to help you meet the training requirements you may need to stay current with caregiver certification and licensure . The more prepared you are, the more secure you feel in your daily work. This is an incredible opportunity to feel great about your job and the impact it has on others. Join our dynamically fun growing team and help bring our unique care philosophy to life! This franchise is independently owned and operated by a franchisee. Your application will go directly to the franchisee, and all hiring decisions will be made by the management of this franchisee. All inquiries about employment at this franchisee should be made directly to the franchise location, and not to Homewatch Caregivers Corporate.

Work Schedule First Shift (Days) Environmental Conditions Office Job Description Discover Impactful work: As a QA Supervisor - Complaint Management​ for Product Complaints, you will be responsible for t he management of a team performing product complaint investigations received from clients. B y working with subject matter experts (SMEs) in the operations areas , you will focus on the compliance of these systems to ensure inspection readiness and to fa cilitate i mprovement in the i nvestigation program. Additionally, as Thermo Fisher Scientific is focused on the customer experience, you will be communicating the status of these items with customers to ensure that their expectations are being met. Key Responsibilities: Collaborate wi th Subject Matter experts (SME), providing independent and objective quality advice supporting business procedures managed by SMEs. Provides Quality oversight related to continuous improvements (CI) associated with our QMS through metrics and key performance indicators. Present i nvestigation findings in r eview b oards (Deviation or CAPA) as well as to the impacted customers Supports the Business Process Owner network by ensuring risk-based improvements to procedures to ensure that they are simple, efficient, and fit for purpose while maintaining regulatory compliance. Lead a team of personnel ensuring team ’s organizational performance and succession planning Direct and prioritize the i nvestigations team to ensure regulatory requirements, client commitments and business needs are met Foster a culture of strong employee engagement, collaboration, flexibility, and competitiveness by improving competence, industry understanding, and executional skills Administer and oversee Thermo Fisher Scientific’s i nvestigation and CAPA computerized systems access, etc. Mentor and train the staff members on i nvestigation process Provide i nvestigation guidance and expertise for complex deviations to all teams on site Supports a robust regulatory intelligence system by monitoring changing regulations and ensuring that the BPO network incorporates changes efficiently and timely . Core Qualities and Competencies: Excellent leadership skills to motivate team to adapt to new ways of working Strive to improve the performance of the team by proactively identifying system improvement opportunities Use critical thinking and engage in problem solving Be able to perform statistical analysis when there is a large body of data Understand and employ risk analysis skills Strong communication skills to effec tively interact with internal teams , regulatory authorities and clients Ability to resolve conflict within the team and in a cross functional setting Excellent o rganizational skills with proven track record to prioritize when timeline conflicts exist Educational and Experience Requirements: Bachelor’s Degree within a Science and/or Engineering field A minimum of 5 years in a cGMP q uality / ma nufacturing role in a pharmaceutical, food or cosmetic environment Experience in management of a team i n a regulatory environment Experience in cGMP principles pertaining to i nvestigations and CAPA Expertise in technical writing skills Exper tise in practical problem solving and continuous improvement projects Experience in direct communication with clients and regulatory authorities Proficient in Microsoft Suite (Word, Excel, PowerPoint) K nowledge of adult learning methodologies; ability to coach and train others Physical Demands: While performing the duties of this job, the employee is required to walk, sit, and use hands, handle or feel tools or controls, reach with hands and arms, balance, stoop, crouch, bend, talk and hear. Typically located in a comfortable indoor area.

Role Summary: As a QA Engineer, you will support the development, implementation, and management of quality control programs and procedures. This position involves translating customer specifications and industry standards into product/process criteria and developing control plans to meet those requirements. You will also address day-to-day production supplier and customer quality issues within the manufacturing plant. Responsible for the development, application, interpretation, and maintenance of quality standards necessary to ensure Flowserve products are in compliance with industry codes and standards. This role involves developing and initiating methods and procedures for inspection, testing, and evaluation of process quality, as well as analyzing and reporting quality data to ensure continuous improvement. You will evaluate supplier quality and collaborate with departments such as Manufacturing, Engineering, and Purchasing to identify and implement supplier improvement opportunities. Additional responsibilities include performing root cause analysis, implementing corrective actions for discrepant material, participating in internal and external audits, and ensuring compliance with ISO 9001 Quality Systems. The role also involves reviewing customer contracts, conducting quality assurance audits, and ensuring product quality and reliability at customer sites and supplier facilities. Location: Springville, UT. Candidates from other locations within the United States will also be considered. Relocation assistance will be provided. Responsibilities: Heavy emphasis on Root Cause Analysis, Corrective and Preventative Actions, ensuring customer satisfaction by addressing quality concerns and implementing improvements. Liaise with manufacturing and inspectors to assist them in performing their functions. Collaborate with other Flowserve departments in conducting quality assurance audits, inspections, and problem-solving activities. Evaluate the need for quality program improvements, identify problems, determine root causes, and recommend or implement appropriate corrective actions. Participate in Continuous Improvement Process (CIP) events Monitor product portfolio KPIs and drive effective root cause corrective actions where appropriate to address gaps to agreed targets Participate in internal and external audits, including supplier evaluations and product/process audits. Perform and coordinate record reviews, information retrieval, and inspection results data input and analysis to ensure quality program compliance and product reliability. Review customer contracts to ensure compliance with contractual requirements. Develop and evaluate supplier performance data, identifying areas for improvement and working with suppliers to create improvement plans. Collaborate with Quality, Manufacturing, Engineering, and Purchasing teams to identify supplier improvement opportunities. Identify specific supplier problems, determine root causes, and recommend or implement corrective actions, including control plans as needed. Perform other duties as directed. Requirements: BS/MS degree in Mechanical, Electronic, Industrial, or Process Engineering. Prior experience as a Quality Engineer or in a similar role, with 5-7 years of experience. Experience in engineering and utilization of Lean and Six Sigma tools and methodologies Advanced understanding of ISO 9001 Quality Systems. Strong interpersonal and communication skills. A proactive approach to identifying and solving quality issues. Proficient in Microsoft Office. Preferred Experience / Skills: Experience in inspections. Knowledge of statistical process control. Proficient in 8D, Pareto Analysis, and other problem-solving techniques. Proficient in Six Sigma analytical techniques. Certified Quality Engineer (CQE) certification is preferred. Oracle experience is a plus. FM Certification (FM Approvals). Other regulatory requirements for IS or EX. Benefits Starting from Day 1: Medical, Dental & Vision Insurance (including FSA and HSA options) Life Insurance + Supplemental Life, Child, Spousal, and AD&D Insurance Short and Long Term Disability Retirement Planning, 401(k) plan, & Financial Wellness Resources Educational Assistance Program Time off Policies (including sick leave, parental leave, and paid vacation) Eligibility requirements apply to some benefits and may depend on job classification and length of employment.

OFF Sun/Thurs 3:45 PM - 2:00 AM Position Summary: The QA Tech 1 is a key Quality Assurance role within the plant and supports QA team leads in safeguarding compliance with food safety and quality requirements. As a QA Tech 1 at Bonduelle Fresh Americas (“BFA”), you will embrace our vision of Giving People the Freedom to Eat HealthierTM through excellence and daily performance of essential quality assurance functions, including finished goods checks and sampling for PCT testing (Hold & Release products). Groupe Bonduelle is a company that is making a positive impact Groupe Bonduelle is the world leader in ready-to-use plant-rich food. By joining our company you will have an opportunity to make a positive and sustainable impact on yourself, others and the planet. You will play an active part in our mission to inspire the transition toward a plant-rich diet to contribute to people's well-being and planet health. Groupe Bonduelle Fresh Americas is the U.S. business unit of France based Groupe Bonduelle ( BON.PA ). We are the first business unit of Groupe Bonduelle to become a Certified B Corporation. We operate three processing facilities throughout the U.S. and employ nearly 3,000 Associates who focus on producing and bringing to market fresh vegetable products, prepared salads and plant-rich meal solutions. Groupe Bonduelle is a 170 year old French family-owned company that has been at the forefront of plant based food innovations since 1853. Our ready-to-use plant-rich food products are grown on 168,000 acres by our grower partners and marketed in nearly 100 countries. The company currently employees more than 11,000 Associates globally. Join us at Bonduelle Fresh Americas for an opportunity to advance your career in a culture that places people first and makes contributing to a better future through plant-based food our top priority. Bonduelle Fresh Americas is a Certified B Corp for a better life. Bonduelle chose B Corporation because of its comprehensive and rigorous standards and its ability to measure a company’s governance as well as worker, community, and environmental impact.We aim to make a positive impact on People, Planet and Food, as seen in our global B!Pact objectives. B Corp certification validates our positive impact and tells the world we are part of a community using business as a force for good. Key Responsibilities: Ensure compliance with and maintain all GMP/PPE/Safety, HACCP & Sanitation guidelines and processes. Understand and implement requirements for product sampling and sample product following PCT sampling procedures established by the customer and corporate QA. Sample finished product for Hold & Release PCT sampling as required by customers; prepares logs and submits samples for Hold & Release tests. Conduct seal integrity tests on finished products and ensure PMOs/SMOs perform equipment adjustments as needed to ensure 100% compliance with seal integrity. Identify any and all non-conformances, document and report it to the PMO/SMO and production leads for immediate follow-up; correct abnormalities and restore functioning where needed. Clean and/or fill-up the Haug tank at the start of every shift and maintain tank water level and cleanliness throughout the shift. Log leaks, non-conformances and sample submissions in the QA database. Perform other duties as assigned. Minimum Qualifications: Strong attention to detail. Ability to read, write and speak English; comprehension of basic math. Basic computer skills and ability to multitask. Willingness and flexibility to work in a cold, wet, fast-paced, 24 hour plant environment. Ability to lift up to 50 pounds, ability to climb stairs numerous times a day. Ability to work independently and in a team environment. GED/High School Diploma. Physical Work Environment: While performing the duties of this job, this position entails use of ladders and catwalks to reach production equipment, regularly works near moving mechanical parts and is regularly exposed to extreme cold for extended periods of time. The associate frequently works in high, precarious places. The associate is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, and risk of electrical shock. The noise level in the work environment is usually loud. Compensation & Benefits: We offer a competitive starting rate of $18.70/hr, commensurate with experience and qualifications. Our comprehensive benefits package includes: Health and Wellness: Medical, Dental, and Vision Insurance with multiple plan options Retirement Savings : 401(k) plan that allows employees to contribute pre-tax dollars to help plan for their financial future with a variety of investment options Paid Time Off: Generous PTO policy, including vacation days, sick leave, and paid holidays Professional Development: Tuition reimbursement program, access to online training courses, and opportunities for career advancement Additional Perks: Employee discount programs, wellness initiatives, and company-sponsored events