CQ Lead – Packaging

QCS Staffing Ltd; Frankfurt; Vor Ort; EUR 90.000 - 120.000; Vollzeit

Zusammenfassung

QCS Staffing Ltd seeks a CQ Lead for packaging systems near Frankfurt, Germany, on an initial 12-month contract in the life sciences sector. The role focuses on leading CQV activities for packaging and integrated production lines, defining strategies and execution plans, and managing cross-functional teams.

The ideal candidate has a degree in engineering or life sciences and extensive pharma/biotech CQV experience on GMP capital projects.

Qualifikationen

• Bachelor's Degree in Engineering, Pharmaceutical Sciences, Biotechnology, Manufacturing Engineering, or related discipline.
• Extensive pharmaceutical/biotech industry experience.
• Strong experience leading CQV/Validation activities on GMP capital projects.
• Proven experience qualifying automated packaging systems.
• Experience supporting startup and operational readiness activities.

Aufgaben

• Lead all CQV activities for packaging systems and integrated production lines.
• Develop and implement CQV strategies, schedules, and execution plans.
• Manage CQV engineers, contractors, and vendor resources.
• Ensure safe execution of commissioning and qualification activities with site EHS standards.
• Drive project schedule adherence and milestone achievement.

Kenntnisse

CQV

Packaging systems

GMP

Project leadership

Ausbildung

Bachelor's Degree in Engineering or life sciences

Jobbeschreibung

CQ Lead – Packaging – Germany, Frankfurt – Initial 12-Month Contract – Life Sciences Looking for your next project? We’re looking for a CQ Lead to join a high-impact pharmaceutical project located near Frankfurt. 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 packaging systems and integrated production lines.
• Develop and implement CQV strategies, schedules, and execution plans.
• Manage CQV engineers, contractors, and vendor resources.
• Ensure safe execution of commissioning and qualification activities in alignment with site EHS standards.
• Drive project schedule adherence and milestone achievement.

Experience required:

• Bachelor's Degree in Engineering, Pharmaceutical Sciences, Biotechnology, Manufacturing Engineering, or related discipline.
• Extensive pharmaceutical or biotechnology industry experience.
• Strong experience leading CQV or Validation activities on GMP capital projects.
• Proven experience qualifying automated packaging systems.
• Experience supporting startup and operational readiness activities.