REQUIREMENTS:

• BSc (Hons) or MSc in Analytical Chemistry or Chemistry.
• Relevant experience in an Analytical Chemistry laboratory.
• Significant expertise in HPLC and Dissolution methods.
• Hands-on expertise and up-to-date knowledge of other analytical methodologies.
• Experience working to GLP and GMP.
  Attention to detail.
  Our Company: “We are a dynamic, fast-growing CRO with a reputation for leading-edge science. We provide contract research services to some of the world’s top pharmaceutical companies, solving complex scientific challenges with integrity and professionalism.
  Our Hoddesdon site in Hertfordshire offers over 5,000 m² of premier R&D space, housing Process Chemistry, Analytical Chemistry, Product Development, and Drug Discovery teams. The site includes state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry.

The Analytical Chemistry team delivers advanced analytical solutions across early- and late-phase pharmaceutical development. You’ll gain exposure to techniques like UHPLC, NMR, and GC-MS, and contribute to method development, validation, and material characterisation. Opportunities also include polymorph screening, crystallisation optimisation, and pre-formulation development—all within a highly supportive, team-focused environment.

• We offer a competitive salary and a progressive and comprehensive suite of employee benefits.
• We offer state of the art working environment on site.
• We offer the opportunity for growth and development and will support funding for relevant training and development programmes.

• Perform analytical testing of drug products, intermediates, and APIs using techniques such as HPLC, Dissolution, KF, Disintegration, and stability analysis.
• Support formulation development projects by developing and validating analytical methods.
• Apply core analytical laboratory skills to positively impact drug product development.
• Design and execute experiments with guidance, interpret results, and plan follow-up work to solve moderately complex analytical problems.
• Collaborate effectively with cross-functional teams including Formulation Development and Materials Characterization.
• Document and report results in line with GMP and internal procedures, contributing to release testing and regulatory submissions.
• Maintain high standards of data integrity, quality, and compliance with GLP/GMP.