As a member of the Analytical Sciences team, you will be involved in and take responsibility for all aspects of the analysis of pharmaceutical and healthcare samples utilising a range of techniques such as LC-MS, GC-MS and ICP-MS. The team specialise in the cGMP analysis of final products, active pharmaceutical ingredients, and excipients with a focus on impurity identification, method development, validation and problem solving for our sponsors.

Job Responsibilities

• Work to laboratory SOPs and adhere to cGMP record keeping and procedures.
• Provide right first-time analytical data to agreed schedules using techniques such as LC-MS, GC-MS or other separation techniques.
• Provide verbal and written reports, both internally and externally.
• Get involved in data review and process improvements.
• Contribute to the Quality Assurance programme of laboratory audits, investigations, and CAPA.