Key Responsibilities
* Perform routine and non-routine analysis of pharmaceutical finished products, and stability samples using HPLC, GC, Dissolution, and other analytical techniques
* Ensure all testing is carried out in compliance with GMP, SOPs, and regulatory requirements
* Accurately document all analytical data, observations, and deviations in accordance with ALCOA+ principles
* Perform equipment calibration, qualification, and routine maintenance as required
* Troubleshoot analytical methods and instruments, and escalate issues when necessary
* Assist in method development and method transfer activities where applicable
* Support laboratory investigations, OOS, and deviation reports with technical input
* Provide support and guidance to junior analysts and contribute to their technical development
* Maintain lab cleanliness, safety, and regulatory compliance at all times
Occasional Duties
* Perform routine analysis of finished products for physical parameters, including: Average Weight, Uniformity of Weight, Disintegration, Friability, Hardness, Water content by Karl Fischer (KF),Identification tests (chemical, UV, IR),Loss on Drying (LOD), and product Description
Candidate Requirements
Minimum Qualifications & Experience:
* A relevant science degree (e.g., Chemistry, Pharmaceutical Sciences, Biochemistry, etc.)
* Minimum of 6* years of experience* in a GMP-regulated pharmaceutical testing laboratory
* Strong hands-on experience with HPLC, GC, and Dissolution is essential
Essential Skills:
* Sound understanding of analytical chemistry principles and GMP compliance
* Familiarity with analytical instruments and software (e.g., Empower, Chromeleon)
* Good organizational, communication, and problem-solving skills
* Ability to work independently and collaboratively in a fast-paced environment
Job Type: Full-time
Pay: £25,500.00-£27,500.00 per year
Benefits:
* Free parking
* On-site parking
Work Location: In person