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Job description

Job Duties & Responsibilities:

• Routine analysis of raw materials, finished goods, stability materials to the appropriate test specification often using HPLC, IR, and UV
• Any non-routine analysis as required by HPLC, IR, and UV
• Ensuring all reagents and volumetric solutions are prepared and available as documented by procedures
• Contribute to the writing of specifications, analytical methods, stability and validation reports
• Organising the sampling and storage of stability samples
• Transfer and validation of new methods
• Implement calibrations of laboratory equipment and ensure that all equipment is maintained in good working order
• Perform cleaning validation and swabbing analysis
• Maintain accurate analysis records in accordance with Good Laboratory Practices
• Maximising laboratory efficiency to meet company turnaround targets
• Proactively solve problems that may arise
• Ensuring traceability by keeping accurate records
• Ensure workplace safety with laboratory equipment, reagents and samples
• Ensure Good Manufacturing and Laboratory Practices are followed in compliance with our licence

Candidate Suitability:

• BSc in Chemistry or a related qualification (required)
• 2 years experience in an analytical role within a pharmaceutical laboratory
• Knowledge of the principles and execution of GMP, analytical method validation and equipment calibration
• Knowledge in the maintenance and use and of HPLC, GC, IR and UV
• Knowledge and experience working to ICH guidelines for stability and validation
• Laboratory Information Management System experience
• Experience working with a variety of wet chemistry techniques
• A desire to work towards performance targets which directly contribute to company performance
• Ability to manage multiple projects and work to the critical timelines of a commercial laboratory

Job Type: Full-time

Salary: £22,000.00-£24,000.00 per year

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday
• No weekends

Work Location: In person