Pharmaceutical Quality Control Analyst

About the Role

Our client is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their laboratory team in Milton Keynes . In this essential on-site role, you will perform a variety of analytical tests on raw materials, intermediate products, and finished pharmaceutical goods to ensure they meet stringent quality and safety standards. Your work will directly contribute to the integrity and reliability of the company's pharmaceutical products, safeguarding public health. This position requires a strong commitment to quality assurance and a hands-on approach within a state-of-the-art laboratory facility.

Key Responsibilities

• Conduct routine testing of raw materials, in-process samples, and finished products using various analytical techniques such as HPLC , GC, and UV-Vis spectroscopy.
• Prepare reagents, solutions, and standards required for analytical testing.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and documentation.
• Accurately record and review test results, investigating any out-of-specification (OOS) results.
• Adhere strictly to established Standard Operating Procedures (SOPs) and safety protocols.
• Participate in method validation and transfer activities as needed.

Requirements

• Bachelor's degree in Chemistry, Pharmaceutical Science, or a related scientific discipline.
• 1-2 years of experience in a pharmaceutical Quality Control laboratory setting.
• Proficiency in analytical techniques including HPLC , titration, and dissolution testing.
• Familiarity with GMP (Good Manufacturing Practice) principles and regulatory requirements.
• Strong understanding of laboratory safety procedures.
• Excellent documentation skills and ability to maintain accurate records.

Benefits

• Competitive starting salary with regular reviews.
• On-site position with a stable, predictable work schedule.
• Comprehensive benefits package including health, dental, and life insurance.
• Pension scheme with company contributions.
• Opportunities for training and development in pharmaceutical quality control.