20 results for Validation Engineer Jobs in New Brunswick, NJ, US

Lead Quality Engineering activities in an FDA-regulated environment, ensuring compliance with cGMP and GAMP 5. Responsibilities include creating quality documentation, performing independent reviews of validation deliverables, collaborating with cross-functional teams to establish validation plans, ...

As a Validation Engineer, you will develop and execute validation and FDA compliance documents for pharmaceutical equipment, assist in managing projects, and help improve client performance. Responsibilities include FAT, SAT, IQ, and OQ documentation development, creating QMS procedures, troubleshoo...

Responsibilities Review computerized systems validation documents such as: Requirements Specification, Design Specification, CSV Risk Assessment, Test Plans, Test Summary Reports, Data Migration Plan, Pre/Post Executed Test Scripts, Traceability Matrix. Release to Production Statements Direct and r...

Location: Skillman, New Jersey Job Type: On-site position (no remote or hybrid options) Effective Date: ASAP (within 2 weeks) Pay range: $50 - $60 per hour FLSA Classification: FT | Non-Exempt Work Authorization: Applicants must have the legal right to work in the United States without requiring spo...

An international biotech company is looking for a fulltime Validation & Operations Engineer to join their growing AI org. This company, located in Princeton, NJ is dedicated to improving the lives of patients through innovative antibody therapeutics.In this role, you will solve operational, validati...

ResponsibilitiesThe Validation Engineer supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers and external service providers. The incumbent in this role contributes to the completion of milestones associated with fac...

Job Description Expert in CSA validation principles.Develop a strategy to convert existing CSV approaches to lab validation into a CSA documented process.Developing, reviewing, and executing testing documentation.Direct experience and understanding of complex lab systems such as HPLC, GC, TOC, UV/Vi...

Responsible for performing cGMP compliance-based services such as commissioning, qualification, validation, and consulting. Duties include writing C/Q/V documents, attending and witnessing FATs and SATs, executing C/Q/V protocols, compiling data and preparing reports. Additionally, assist in deviati...

Company Description Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Res...

1. PURPOSE AND SCOPE OF POSITION: The Validation Engineer supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers and external service providers. The incumbent in this role, contributes to the completion of milestones ...