- 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
- Kelly Services (Pennington, NJ)
- …standards from design through production. Job Duties include: + Creating and implementing validation protocols ( IQ , OQ , PQ) for equipment, utilities, and ... Kelly Science is seeking a Validation Engineer for a growing company located in Pennington, NJ. Summary: As a Validation Engineer , you will be… 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 (Princeton, 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
- BeiGene (Hopewell, NJ)
- …for project activities including review of validation documentation and attendance at validation activities (FAT, SAT, IQ , OQ , PQ) etc. + Ensure ... review of validation documentation and attendance at validation activities (FAT, IQ , OQ ,...required to work closely with both manufacturing, quality, and engineer associates. + Maintaining the validation sample… 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
- J&J Family of Companies (Raritan, NJ)
- …Device environmental chamber, photo chamber, packaging and physical testing equipment IQ / OQ /PQ. + Implement initiatives to improve efficiency, cycle times ... Senior Biomaterials Scientist/ Engineer - 2406208855W **Description** Ethicon, a member of Johnson & Johnsons family of companies, is recruiting for an Biomaterials… 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
- AbbVie (Branchburg, NJ)
- …specifications for process control systems for projects. + Support IQ / OQ development and participate in systems analysis, validation , and verification. + ... new product technology transfer + Assists project teams in developing sterilization validation strategies. + Actively collaborate with the project teams to support… more