QC/RnD Analyst

Strategic Partners, on behalf of a client in the pharmaceutical sector, is seeking a QC / R&D Analyst to join their laboratory team.

This position plays a key role in ensuring the quality, safety, and compliance of pharmaceutical products. The successful candidate will carry out analytical testing on raw materials, in-process samples, and finished products while supporting continuous improvement initiatives within the laboratory.

Main Responsibilities

• Perform analytical and wet chemistry testing on raw materials, intermediates, and finished products in alignment with GMP standards.
• Operate and maintain advanced analytical instruments, including HPLC, GC, UV-Vis, FTIR, Dissolution apparatus, and Karl Fischer titrator.
• Accurately document and review results in compliance with GLP and Data Integrity (ALCOA+) guidelines.
• Contribute to OOS (Out-of-Specification) and OOT (Out-of-Trend) investigations, supporting root cause analysis.
• Calibrate and troubleshoot laboratory equipment as needed.
• Ensure compliance with international guidelines (ICH, FDA, EMA, WHO).
• Support method validation, verification, and transfer projects.
• Collaborate closely with QA and Production teams to ensure timely release of materials and products.
• Actively participate in continuous improvement initiatives for laboratory efficiency and compliance.

Candidate Profile

• B.Sc. or M.Sc. in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related field.
• 1–3 years of professional experience in a pharmaceutical QC laboratory (junior-level candidates may also be considered).
• Hands-on knowledge of analytical techniques (HPLC, GC, Dissolution, FTIR, UV).
• Solid understanding of GMP, GLP, and regulatory standards.
• Familiarity with LIMS and electronic documentation systems is a plus.
• Strong analytical and problem-solving skills, with attention to detail and accuracy.
• Ability to work effectively both independently and within a team.
• Good communication and reporting skills.

What's Offered

• euros gross salary
• Private health insurance
• Ongoing training, professional development, and certification opportunities.
• Exposure to modern pharmaceutical technologies and global regulatory practices.
• A collaborative, growth-oriented, GMP-compliant work environment.