Senior Pharmaceutical Quality Control Analyst

About the Role

Our client is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory facility in Leicester . This pivotal role involves overseeing critical quality assurance processes to ensure all pharmaceutical products meet rigorous regulatory standards and internal specifications. You will be instrumental in maintaining the integrity and safety of our client's pharmaceutical output, contributing directly to their reputation for excellence. This position offers a significant opportunity to make an impact within a leading pharmaceutical company that values precision, scientific rigor, and career development for its dedicated professionals.

Key Responsibilities

• Perform a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques, including HPLC, GC, and spectrophotometry.
• Develop, validate, and transfer analytical methods according to established protocols and regulatory guidelines.
• Interpret complex analytical data, identify trends, and investigate any out-of-specification (OOS) results, implementing corrective and preventative actions (CAPAs).
• Maintain accurate and comprehensive laboratory records, ensuring compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards.
• Collaborate with R&D, production, and regulatory affairs teams to resolve quality issues and support product development lifecycles.
• Mentor and train junior analysts, providing guidance on technical procedures and quality standards.

Requirements

• Bachelor's degree in Chemistry, Pharmaceutical Science, or a related scientific discipline.
• Minimum of 3-5 years of experience in a pharmaceutical Quality Control or Analytical Development role.
• Proficiency in operating and maintaining common analytical instrumentation, with expertise in HPLC and GC .
• Thorough understanding of pharmaceutical quality systems, regulatory requirements (e.g., MHRA, FDA), and GMP guidelines.
• Strong problem-solving abilities, excellent attention to detail, and accurate data recording skills.

Benefits

• Competitive starting salary and potential for performance-based bonuses.
• Generous holiday allowance and company pension scheme.
• Opportunities for professional development, training, and career advancement within the pharmaceutical sector.
• Access to cutting-edge laboratory equipment and technology.
• A supportive team environment committed to scientific excellence and product quality in Leicester .