Head of Quality Control

Optimus Life Sciences

Nordrhein-Westfalen

Sur place

EUR 110 000 - 160 000

Plein temps

Il y a 12 jours

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Résumé du poste

Optimus Life Sciences in North Rhine-Westphalia seeks a Head of Quality Control to lead the on-site QC function in a GMP environment. This senior role oversees a team of experienced laboratory professionals and ensures day-to-day QC operations meet regulatory standards.

The successful candidate will drive method validation/transfer, maintain audit readiness, and collaborate with Quality, Production and R&D to continuously improve processes. Fluency in German and professional English is required.

Qualifications

  • Extensive leadership experience in a GMP QC lab.
  • Strong technical foundation in analytical chemistry and HPLC.
  • Experience with method validation and transfer.
  • Experience with deviations, OOS and GMP quality systems.
  • Fluent German and professional English.

Responsabilités

  • Lead the QC team and drive development of the department.
  • Plan laboratory workload and coordinate testing activities.
  • Ensure GMP compliance and inspection readiness.
  • Oversee analytical activities including HPLC, validation, and transfers.
  • Manage deviations, OOS investigations, change controls, and troubleshooting.
  • Support qualification of lab equipment and methods.
  • Represent QC in customer audits and technical discussions.
  • Collaborate with Quality, Production and R&D functions.
  • Pursue continuous improvement of lab processes and efficiency.

Connaissances

Leadership
GMP QC
HPLC
Method Validation
Audit Readiness
Troubleshooting
Analytical Chemistry
German & English

Description du poste

Head of Quality Control | Pharmaceutical / CDMO | NRW

I'm supporting an established pharmaceutical organization in North Rhine-Westphalia with the appointment of a Head of Quality Control to lead its on-site QC function.

This is a senior, hands-on leadership position within a GMP-regulated environment, taking responsibility for a team of experienced laboratory and analytical professionals.

The role

You will take overall responsibility for the day-to-day operation and development of the Quality Control department, including:

  • Leadership and development of the QC team
  • Planning and coordination of laboratory workload and testing activities
  • Ensuring continued GMP compliance and inspection/audit readiness
  • Oversight of analytical activities including HPLC, method validation and method transfer
  • Management of deviations, OOS investigations, change controls and troubleshooting
  • Supporting qualification of laboratory equipment and analytical methods
  • Representing QC during customer audits and technical discussions
  • Close collaboration with Quality, Production and Process/R&D functions
  • Continuous improvement of laboratory processes, structures and efficiency
Your background

We are interested in speaking with experienced pharmaceutical QC professionals who bring:

  • Strong experience within GMP pharmaceutical Quality Control
  • Leadership experience within a QC laboratory environment
  • A strong technical foundation in analytical chemistry / HPLC
  • Experience with method validation, method transfer and analytical troubleshooting
  • Good knowledge of deviations, OOS and GMP quality systems
  • Confidence interacting with customers and supporting audits
  • A practical, hands-on leadership style suited to a smaller, fast-moving organization
  • Fluent/native-level German and professional English

Predominantly on-site position

Leadership responsibility for an established QC team

This is an opportunity to take genuine ownership of a QC function within a business where the Head of QC has direct visibility and influence across the organization.

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