QA Engineer - $64/hr w2. Charlotte, NC Must be STRONG Python developers, literally SME's They MUST have Fixed Income Derivatives/Capital Markets experience. If not, DO NOT SUBMIT t...
About US: Tryfacta is a leading, nationally renowned Workforce Management Solution provider for private &public sector firms across the US. We specialize in Healthcare, IT, Busines...
Job Title: Technical Services Coordinator Reports to: Head of QALocation: Lewisville, TX Job Type: Full-time/Non-Exempt Business Hours: M-F 9:00 AM - 5:30 PM Work hours may vary fr...
Employment Type: Hourly Shift: Third Work Arrangement: Onsite Position Summary: Assist Quality Assurance (QA) Supervisor in supervising and coordinating all QA activities within th...
Typically, 5-7 years of work experience in IT or business environment and/or BS/BA or MBA/MS in computer science, engineering, information systems, math or business. Knowledge of t...
This job description is a general description of the essential job functions and is not intended to be an employment contract. Eastern Shipbuilding Group, Inc. maintains its status...
AMP United is a TURNKEY industrial preservation contractor specializing in large-scale surface preparation, coating application, containment, and scaffolding across the U.S. With p...
Our Client, a Banking company, is looking for a Senior QA Lead for their Brooklyn, OH location. Responsibilities: Leads the QA team for a large transformational project and may lea...
Title: QA Laboratory Technician I Duration: 3 months Location: Commerce, CA 90040 Shift : Schedule 3 AM - 11: 30AM - Candidate to be flexible for change of hours Candidate to be op...
QA Clerk JOB SPECIFICS: Perform pre operational GMP line inspections. Assists in monitoring and enforcing GMP and Safety rules. Assist in training new FSQA Technicians on job respo...
OB TITLE: QA/QC- Electrical SUMMARY: Quality Control inspection and associated documentation of Electrical systems within a cleanroom environment. DUTIES AND RESPONSIBILITIES: Coor...
Start or transition your career into Software Quality Assurance. Ace IT Careers is currently identifying candidates for QA Software Tester opportunities with employers and staffing...
If you have experience inspecting production hardware, supporting DCMA sell-off, and working in a fast-paced manufacturing or defense environment, this is the kind of role where yo...
Job TitleConstruction Site ManagerJob DescriptionLead and oversee project-specific Quality Assurance and Quality Control (QA/QC) programs. Develop, implement, and maintain quality...
QA AssociateA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has...
Experience with Kneat is absolutely required. Experience with Ellab for Temp Mapping is a plus
Manager is looking for candidates with Cleaning Val (CIP, COP, SIP). 95% of equipment is Single Use, so the Cleaning Val is limited mostly to Media Hold/Media Fill. Cleaning Val is mostly Drafting SOPs
Other equipment includes Autoclaves, Parts Washers, and Storage equipment (cold and ambient). Looking for the worker to Build Equipment Re-qualifications in Kneat.
Provide Subject Matter Expert support to Quality Control, Manufacturing and other departments for the design, operation and troubleshooting of equipment.
Drive/own the validation plans and execution of equipment changes and process improvements.
Perform Equipment Validation activities to include Validation Maintenance Quality Systems review and requalification to ensure GMP equipment is continuously maintained in a validated states.
Demonstrate a general understanding of biopharmaceutical manufacturing equipment and validation procedures for Installation Verification (IV/IQ), Clean-In-Place (CIP), Steam-In-Place (SIP), Autoclaves, Clean Utilities, Shipping Validation, Temperature Mapping Controlled Storage Rooms and Equipment.
Program, organize, and maintain Validation equipment and supplies including dataloggers and probes
Develop validation protocols from plans and engineering documents.
Perform assigned Quality Systems activities within Document Management System (DMS), TrackWise Quality System (Change Control, Deviation, CAPA)
Perform other duties as assigned.
Provide basic technical support when reviewing and approving SOPs, Protocols, Change Controls, Deviations, CAPA, etc.
Job Summary: Equipment Validation Analyst Execution of Installation Qualifications/Operational Qualifications and drafting Performance Qualifications as required.
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