Validation jobs in Elizabeth, New Jersey (NJ) State

Experience in sub-systems, systems engineering, requirement development and/or requirement validation, developing RF electrical subsystems and electrical hardware development. GPS Subsystem Engineer collaborates with missile level system engineers in developing requirements for the subsystem. Q.....

As the validation engineer you'll be responsible for writing validation protocols (IQ/OQ) as well as validating large complex manufacturing equipment in the Pharma & Life Sciences industries. Presenting the validation results to end customer project teams (QA, validation, project management, etc....

Minimum 3-5 years of experience with Computerized System Validation (CSV), Equipment Validation, and/or Process Validation required. Novartis is seeking a seasoned QA (Quality Assurance) Validation Specialist to support the strategic implementation of quality and validation objectives. Act as SME...

Develops validation/qualification deliverables such as Validation Plans, Requirements. The Equipment Validation Engineer supports the successful implementation of various process/lab. Supports the execution of equipment qualifications and validation protocols. Supports equipment qualification and...

Develops validation/qualification deliverables such as Validation Plans, Requirements. Supports the execution of equipment qualifications and validation protocols. Supports equipment qualification and validation activities. Completes all qualification and validation documentation with accuracy, c...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES ...

Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls. The Equipment Validation Engineer supports the successful implementation of various process/lab equipment at multi-use sites through inter...

Support validation activities for project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ, OQ, PQ) and attendance at validation activities. Ensuring appropriate investigation of validation discrepancies, errors, protocol failures, or validation testing errors requi...

Must Have: Develops validation/qualification deliverables such as Validation Plans, Requirements. Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls. Engineering - Validation Engineer. The E...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe ...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. Specialist, MSEO Manufacturing Systems Validation. Specialist, MSEO Manufacturing Systems Valid...

Modem system validation engineer. ...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES ...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES ...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES ...

Develops validation/qualification deliverables such as Validation Plans. The Equipment Validation Engineer supports the successful implementation of various process/lab equipment at multi-use sites through interaction with internal customers and external service providers. Knowledge of cGMP, GXP,...

Must feel comfortable wearing multiple hats, from helping to design and implement new SW modules for validation, to leading the debugging of a HW issue in the lab, putting together a validation schedule; and anything in-between. We are looking for a passionate Staff System Software Validation Eng...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. On-Board Services is hiring a Validation Specialist. The Specialist will partner with site Busine...

In this role, you will work closely with the NA Digital Consumer Team, product owners, Tech Team, and other members of the Operations group in testing, implementing, and managing products, processes, user acceptance testing and data validation to dramatically improve the customer experience. Succ...

Support validation activities for project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ, OQ, PQ) and attendance at validation activities. Ensuring appropriate investigation of validation discrepancies, errors, protocol failures, or validation testing errors requi...

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KEY RESPONSIBILITIES AND ACTIVITIES Develop Master Validation Plans for communicating commissioning, qualification and validation approach and requirements. Pharmaceuticals, Biotechnology, Medical Devices, Cell & Gene Therapy) Experience working on regulatory and compliance environments · B...

The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing. The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES ...

Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment and control systems. Create and modify validation documentation including but not limited to: User Requirements Specifications (URS) Design Reviews (DR) Criticality assessments CSV prot...