CQV Engineer

Devens, MA, US • Posted 19 hours ago • Updated 6 hours ago
Full Time
On-site
Fitment

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Job Details

Skills

  • SIP
  • Testing
  • Mapping
  • Chromatography
  • Collaboration
  • Quality Assurance
  • Quality Control
  • Manufacturing
  • IQ
  • OQ
  • Cell Culture
  • GMP
  • GDP

Summary

Summary :

We are looking for hands-on CQV Engineers to support a high-impact biologics project within a GMP-regulated environment. This is a fast-paced opportunity focused purely on execution of validation protocols-ideal for professionals who thrive on the manufacturing floor.

Roles & Responsibilities:
  • Execute IQ/OQ protocols for process equipment
  • Perform equipment walkdowns and verify against design
  • Support SIP/CIP cycles, wet testing, and temperature mapping
  • Work with downstream equipment (chromatography, filtration, tank farms, etc.)
  • Document and execute validation activities in ValGenesis
  • Collaborate with QA/QC and Manufacturing teams

Education & Experience :
  • Strong experience in CQV / Validation (IQ/OQ)
  • Background in biologics / biopharma / cell culture
  • Hands-on experience with process equipment validation
  • Familiarity with GMP & GDP practices
  • Experience with downstream equipment
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91116760
  • Position Id: 70caee7cf4ce4ac7192b8d4bd57c5adb
  • Posted 19 hours ago
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