Quality Control Scientist – Pharmaceutical Analysis

About the role

We are seeking a Quality Control Scientist to join Kymos’ Pharmaceutical Chemical Analysis department. The role focuses on the analysis of active pharmaceutical ingredients and drug products, ensuring compliance with regulatory standards and supporting product development.

Key responsibilities

• Design, develop, and validate analytical methods for drug control and stability studies.
• Perform routine testing using techniques such as HPLC, GC, potentiometry, Karl Fisher titration, UV spectroscopy, and dissolution testing.
• Draft, review, and manage technical documentation including protocols, reports, standard operating procedures, and certificates of analysis.
• Supervise and mentor laboratory analysts, promoting scientific excellence and GMP compliance.
• Collaborate with cross‑functional teams to support quality assurance and regulatory submissions.

Required profile

• Bachelor’s degree in Chemical Sciences with an analytical focus; a Master’s degree is highly valued.
• Basic knowledge of HPLC and GC techniques and familiarity with analytical development processes.
• Experience in method development and validation for pharmaceutical quality control is preferred.
• Previous work in a Quality Control or Analytical Development environment within the pharmaceutical sector.
• Understanding of GLP and GMP requirements.
• English proficiency at First Certificate level.

Required skills

• HPLC
• GC
• Potentiometry
• Karl Fisher titration
• UV spectroscopy
• Dissolution testing

What we offer

• Dynamic, growing team with professional development opportunities.
• Hybrid work model with flexible hours and an intensive Friday schedule.
• Access to employee benefits platform, 23 vacation days plus holidays, and a fully stocked canteen.
• Modern headquarters in Cerdanyola del Vallés with rooftop terrace and green surroundings.