Latest Computer System Validation Pharmaceutical jobs in Bridgewater, NJ

21 Computer System Validation Pharmaceutical Jobs in Bridgewater, NJ

Validation Engineer Innova Solutions - Summit, NJ, United States , computer systems validation requirements and good documentation practices. Experience in the qualification of cell therapy equipment a plus Advanced knowledge of pharmaceutical, manufacturing and laboratory 5 days ago
Equipment Engineer Pyramid Consulting, Inc - Warren, NJ, United States audits. Key Requirements and Technology Experience: Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices 5 days ago
Senior Execution Systems Engineer, CAR-T Johnson and Johnson - Raritan, NJ ), Computer System Validation (CSV), and Data Integrity (DI) standards, including FDA 21 CFR Part 11. * Ability to Work Cross-Functionally, Influence Decision Making, and Present to Leadership. * Excellent 5 days ago
Equipment Validation Engineer Dexian - Summit, NJ, United States and collaborative relationships outside the immediate organization. REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: * Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems 5 days ago
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Equipment Validation Engineer Pyramid Consulting, Inc - Summit, NJ, United States , computer systems validation requirements and good documentation practices. Experience in the qualification of cell therapy equipment a plus. Advanced knowledge of pharmaceutical, manufacturing and laboratory 5 days ago
Lead, Technology Compliance Johnson & Johnson - Raritan, NJ Pharmaceutical/Medical Device company or minimum of 2 years of direct experience with GxP Quality Assurance, development, implementation and/or validation of computerized systems within Pharmaceutical/Medical USD 90,000.00 - 144,900.00 per year 10 days ago
Equipment Commissioning & Qualification Engineer LanceSoft, Inc. - Summit, NJ, United States , GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. Experience in the qualification of cell therapy equipment a plus. Advanced 6 days ago
Equipment Engineer Eclaro - Warren, NJ, United States . REQUIRED COMPETENCIES: Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. Knowledge of pharmaceutical 28 days ago
Senior Execution Systems Engineer, CAR-T Johnson & Johnson - Raritan, NJ : Required: A Minimum 4 years experience in MES (PAS-X) eBR Development and Master Data Management in a Pharmaceutical Manufacturing System/Process (GxP) environment. Working Knowledege of ISA-88 (Standards USD 76,000.00 - 121,900.00 per year 24 days ago
Senior QA Systems Auditor - Home Based, UK IQVIA - Livingston, UK , qualification protocols, phase reports and summary reports. Expert knowledge of Computer Systems Validation in a life science or regulated environment required. Experience with software validation and testing 5 days ago

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