CQV Engineer

Join an innovative and fast-growing biotechnology company in Massachusetts. As the CQV Engineer, you'll play a critical role in supporting GMP manufacturing operations by leading commissioning, qualification, and validation activities across state-of-the-art facilities, equipment, and utilities.

• High-Impact Projects:
  Lead CQV activities supporting manufacturing expansion and operational readiness.
• Cross-Functional Exposure:
  Partner with teams including on technical matters and projects

We're seeking an experienced CQV Engineer with a strong background in GMP-regulated environments. You'll have proven experience executing validation activities while driving projects through to successful completion.

As the CQV Engineer, you will:

• Lead qualification and validation activities to support GMP manufacturing operations and new engineering projects.
• Develop and maintain technical documentation to ensure systems meet regulatory and quality requirements.
• Support the delivery of engineering projects from installation through to operational handover.
• Partner with multidisciplinary teams to ensure successful implementation of new equipment and manufacturing capabilities.
• Contribute to continuous improvement initiatives that enhance compliance, reliability, and operational performance.

• 5+ years of CQV expertise from a GMP-regulated environment
• Expertise in equipment, utilities and manufacturing facilities

Join a fast-paced, international business focused on providing life‑saving medicines to patients globally. You'll have the opportunity to lead impactful projects, collaborate with high-performing teams, and contribute to advancing innovative therapies in a dynamic and growing organization.

If this opportunity is of interest, please reach out to Guled Samatar at Meet Life Sciences

• Call:
• Email: guled