Quality Control Specialist II

About the role

The Quality Control Specialist II will support reliable laboratory operations within the QCMD team, ensuring compliance with high quality standards and regulatory requirements. You will contribute to safe product delivery by overseeing testing activities and supporting continuous improvement.

Key responsibilities

• Oversee production and testing activities to ensure compliance with cGxP, data integrity and e‑Compliance requirements.
• Review and approve QC testing results, production documentation, QC records and AS&T records.
• Support deviation, investigation and CAPA processes with timely follow‑up and documentation.
• Ensure analytical equipment qualification, calibration status and laboratory documentation are maintained.
• Contribute to audit and inspection readiness and support batch release activities.

Required profile

• Education as a Lab Technician or a university degree in chemistry, pharmacy, biology or related field.
• Professional experience in a GMP‑regulated pharmaceutical laboratory (QC, QA or analytics).
• Strong knowledge of GMP and GxP standards, quality control testing and documentation.
• Good communication skills in German and English and ability to work collaboratively across QC, QA, production and operational teams.

Required skills

• GMP and GxP compliance
• Analytical equipment qualification and calibration
• Laboratory data integrity management
• Quality control testing procedures

What we offer

• Market‑competitive base salary with a range of €60,978 – €95,800 per year.
• Attractive incentive program, pension scheme, childcare facilities and learning & development opportunities.
• Flexible and hybrid working options where possible and a minimum of 14 weeks paid parental leave.