🛠 Tech Stack

💼 About This Role

You'll lead commissioning and qualification of biopharmaceutical equipment, supporting upstream and downstream operations. You'll author and execute C&Q protocols and collaborate with multi-disciplinary teams for GMP drug manufacturing projects. This role offers the opportunity to work with bioreactors and filtration systems in a 100% employee-owned company.

🎯 What You'll Do

• Lead conceptual, basic, and detailed design for process equipment and utilities.
• Author, review, and execute C&Q protocols (IQ/OQ/PQ).
• Collaborate with cross-functional teams including Automation and Manufacturing.
• Coordinate engineering consultants, equipment vendors, and contractors.

📋 Requirements

• Bachelor's degree in Chemical, Biotechnology, or Biochemical Engineering.
• 3–5+ years of hands-on experience in downstream bioprocess operations.
• Experience with full lifecycle C&Q of biopharmaceutical equipment.
• Willingness to travel up to 50%.

✨ Nice to Have

• Upstream bioprocess experience.
• Siemens PCS7 or DeltaV experience.
• Senior-level C&Q engineer background.