CQ Lead – Clean Utilities

Association of Academic Physiatrists; Frankfurt; Vor Ort; EUR 90.000 - 150.000; Vollzeit

Zusammenfassung

The Association of Academic Physiatrists seeks a CQV Lead to join a high-impact pharmaceutical project near Frankfurt. You will own commissioning and qualification activities for clean utilities and support global life-sciences manufacturing initiatives.

Lead CQV strategies, manage engineers and contractors, and drive safety, deviations, and risk mitigation to milestone completion on a GMP capital project. Initial 12-month contract.

Qualifikationen

• Extensive experience in pharmaceutical/biotech/life sciences industries.
• Proven track record leading CQV or validation on GMP capital projects.
• Experience qualifying pharmaceutical utility systems.
• Experience delivering greenfield GMP manufacturing facilities.
• Strong experience supporting sterile manufacturing or fill-finish facilities.

Aufgaben

• Lead all CQV activities for clean utility generation, storage, and distribution systems.
• Develop CQV strategies, validation plans, and execution schedules for utility packages.
• Manage CQV engineers, contractors, and vendor resources to deliver milestones.
• Promote a safety-first culture throughout commissioning and qualification activities.
• Drive issue resolution, deviation management, and risk mitigation.

Jobbeschreibung

CQV Lead – Clean Utilities– Germany, Frankfurt – Initial 12-Month Contract – Life Sciences

Looking for your next project? We’re looking for a CQ Lead tojoin a high-impact pharmaceutical project located nearFrankfurt. With major capital investment experience driving various facility build projects. This is a unique assignment for a CQ Lead to support a global leader in the life sciences market and play a key role in shaping the future of advanced manufacturing.

What you’ll deliver:

• Lead all CQV activities associated with clean utility generation, storage, and distribution systems.
• Develop CQV strategies, validation plans, and execution schedules for utility packages.
• Manage CQV engineers, contractors, and vendor resources to deliver project milestones.
• Promote a safety-first culture throughout commissioning and qualification activities.
• Drive issue resolution, deviation management, and risk mitigation activities.

Experience required:

• Extensive experience within pharmaceutical, biotechnology, or life sciences industries.
• Experience leading CQV or Validation activities on GMP capital projects.
• Demonstrated experience qualifying pharmaceutical utility systems.
• Experience delivering greenfield GMP manufacturing facilities.
• Strong experience supporting sterile manufacturing or fill-finish facilities.

Don’t miss your chance to be part of something extraordinary!