Quality Specialist – Pharmaceutical QC

About the role

We are looking for a Quality Specialist to join the Quality Control team at a pharmaceutical production site in Saarland. The role supports GMP‑compliant release of raw materials, intermediates and finished products and contributes to continuous improvement of analytical processes.

Key responsibilities

• Support GMP‑based approval of raw materials, intermediates and finished products by reviewing analytical data.
• Evaluate and interpret laboratory test results against specifications and quality standards.
• Oversee laboratory activities to ensure compliance with GMP regulations and internal procedures.
• Perform independent checks of analytical data for accuracy and consistency.
• Investigate out‑of‑specification results, identify root causes and implement corrective and preventive actions.
• Identify and drive process improvements, including the introduction of new analytical techniques or systems.
• Draft, update and maintain SOPs in line with regulatory requirements.
• Assist in internal and external audits and follow‑up on audit actions.
• Document and report all QC activities according to GMP standards.
• Provide training and guidance to laboratory staff and support onboarding of new methods and technologies.

Required profile

• Degree in Pharmacy or equivalent qualification meeting §15 AMG requirements.
• Initial experience in pharmaceutical quality control within a GMP‑regulated environment.
• Strong understanding of GMP, ICH guidelines and regulatory expectations.
• Analytical mindset with high precision in handling test results and deviations.
• Fluent German (C1) and good English (B1 or higher).

Required skills

• HPLC
• GC
• UV/VIS
• Laboratory information systems
• MS Office

What we offer

• Stable position within an international, quality‑focused environment.
• Opportunities for professional development and career growth.
• Collaborative and inclusive working culture.
• Exposure to modern pharmaceutical production and quality systems.