GMP Project/Site Engineer – Pharma & CQV Focus
Novozen Healthcare LLC
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Job summary
Novozen Healthcare LLC is seeking a Project/Site Engineer in Massachusetts specializing in GMP pharma/biotech. The candidate will provide engineering support for manufacturing systems and compliance activities related to GMP documentation.
Ideal applicants should have a Bachelor's degree in Engineering, 4+ years of relevant experience, and familiarity with CQV documentation. Experience with BMS, EMS, and SCADA systems is preferred. The role offers a chance to work in a dynamic, regulated environment.
Qualifications
- 4+ years of GMP pharma/biotech manufacturing experience.
- Experience with CQV documentation and change controls.
- Knowledge of BMS, EMS, SCADA, and CMMS systems.
Responsibilities
- Provide engineering support for GMP manufacturing, facilities, and utilities.
- Support change controls, deviations, CAPAs, and GMP documentation.
- Assist with CQV activities including FAT/SAT, IQ/OQ/PQ.
Skills
Education
Tools
Job description
Novozen Healthcare LLC is seeking a Project/Site Engineer in Massachusetts specializing in GMP pharma/biotech. The candidate will provide engineering support for manufacturing systems and compliance activities related to GMP documentation.
Ideal applicants should have a Bachelor's degree in Engineering, 4+ years of relevant experience, and familiarity with CQV documentation. Experience with BMS, EMS, and SCADA systems is preferred. The role offers a chance to work in a dynamic, regulated environment.
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