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Senior Analytical Development Scientist – GMP & Validation
Job summary
A leading pharmaceutical contract manufacturer in the UK seeks a Development Analyst to conduct analysis and provide technical expertise in a fast-paced environment. The ideal candidate has a strong background in pharmaceutical analysis, with proficiency in analytical techniques like HPLC and Gas Chromatography. The role requires a results-oriented individual, able to work independently and communicate effectively. Candidates must have a minimum of 3 years relevant experience and understanding of GMP regulations.
Qualifications
- Experience of 3+ years in a pharmaceutical or biotechnology industry.
- Understanding of drug development and manufacturing processes.
- Competence in writing reports for internal and external use.
Responsibilities
- Conduct analysis to support formulation development.
- Perform method development and validation for analytical methods.
- Check analytical data and writing protocols and reports.
Skills
Tools
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.