- System One (Somerset, NJ)
- Title: Validation Engineer IQ , OQ , PQ Hours: Mon- Fri 8:30-5:00pm Location: Greater Somerset, NJ area Type: Direct Hire Requirements: + Bachelor's degree ... Develop and implement validation protocols, including Installation Qualification ( IQ ), Operational Qualification ( OQ ), and Performance Qualification (PQ) for… more
- Verista (New Brunswick, NJ)
- …scripts + General understanding of capital equipment implementation and process knowledge + Understanding validation documents, URS, IQ , OQ , PQ + Lead CQV ... including HVAC, water systems, and building automation. + Develop and execute IQ / OQ /PQ protocols for clean utilities and facility systems. + Collaborate… more
- Verista (New Brunswick, NJ)
- …automated systems, including document control and archiving. + Perform quality reviews of IQ / OQ /PQ protocols, test scripts, and validation reports. + ... automated systems, including document control and archiving. + Perform quality reviews of IQ / OQ /PQ protocols, test scripts, and validation reports. +… more
- Integra LifeSciences (Plainsboro, NJ)
- …and productivity. + Process Validation and Documentation: Develop and execute validation protocols ( IQ , OQ , PQ) for manufacturing processes, ensuring ... and making headway to help improve outcomes. The Manufacturing Engineer II will play a key role in driving...batch processing, packaging, and sterilization. + Proficiency in process validation methodologies ( IQ , OQ , PQ),… more
- Actalent (Somerset, NJ)
- …project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ , OQ , PQ) and attendance at validation activities. Providing ... Job Title: CQV Engineer Job Description Assisting in development, review, and...of cGMP documents including, but not limited to: Master Validation Plans, FAT/SAT documents, Turnover Packages, SOP's, specifications, traceability… more
- Verista (New Brunswick, NJ)
- …scripts + General understanding of capital equipment implementation and process knowledge + Understanding validation documents, URS, IQ , OQ , PQ + Develop and ... our experiences to enhance our collective expertise Lead CSV Engineer /Analyst Responsibilities: + Authoring, editing, and executing technical commissioning,… more
- Integra LifeSciences (Plainsboro, NJ)
- …procedures and statutory requirements (US FDA and ISO). + Initiate, develop and implement IQ / OQ /PQ validations for equipment and processes to meet the demands of ... and making headway to help improve outcomes. The Manufacturing Engineer I will play a key role in the...with Quality System Regulation (QSR), Design Control and Process Validation guidelines, Engineering Change Controls, ISO, Design Control and… more