GMP Project/Site Engineer – Pharma & CQV Focus

Novozen Healthcare LLC

Massachusetts

On-site

USD 80,000 - 100,000

Full time

14 days+

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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

GMP documentation
Engineering support
Change controls
CQV documentation
Troubleshooting

Education

Bachelor’s degree in Engineering or related field

Tools

BMS
EMS
SCADA
CMMS

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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