Qc Analyst

About the Role

BSP Pharmaceuticals is a leading Contract Development and Manufacturing Organization (CDMO) specializing in the development and manufacturing of highly potent and cytotoxic anticancer drugs. Since 2006, BSP has been dedicated to innovation in the fight against cancer, investing in new technologies and production methods within a high containment facility. We are seeking a motivated Quality Control Analyst to join our team in Latina, Italy.

Key Responsibilities

• Perform quality control testing on raw materials, in-process samples, and finished products.
• Ensure compliance with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Operate and maintain laboratory equipment.
• Document all testing procedures and results accurately.
• Participate in method validation and transfer activities.
• Contribute to investigations and corrective actions as needed.

Requirements

• Proven experience in Quality Control within the pharmaceutical industry.
• Familiarity with the manufacturing of anticancer drugs and cytotoxic compounds.
• Strong understanding of GMP principles.
• Excellent analytical and problem-solving skills.
• Ability to work independently and as part of a team.
• Proficiency in English.

What We Offer

• A permanent contract with a leading pharmaceutical company.
• The opportunity to work on cutting-edge anticancer drug development.
• A dynamic and innovative work environment.
• Onsite position in Latina, Italy.