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| Job Location | Swadlincote |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Job Title: Stability AnalystLocation: DerbyshireSalary: 26-32K D.O.EMy client are dedicated to excellence in pharmaceutical testing and research. We uphold the highest standards in cGMP/GLP compliance and are seeking a meticulous and proactive Stability Analyst to join our Validation and Stability team. If you are a recentchemistry graduate with a year in industry – I want to speak to you!Key Responsibilities:• Conduct analytical testing according to cGMP/GLP, SOPs, and Work Instructions, with a focus on QC analytical project testing and stability testing.• Assist with the stability program, including generating protocols, reports, trial discontinuation, and stability data tables.• Initiate stability trials and maintain stability program product trending.• Perform maintenance checks of stability cabinets and assist with laboratory documentation upkeep.• Act as a signatory for laboratory documentation, Work Instructions, and SOPs as an author or reviewer.• Advise senior staff on instrumentation and equipment deficiencies, proactively addressing potential delays or problems.• Troubleshoot analytical and equipment issues and investigate Out of Specification (OOS) results with line management assistance.• Carry out calibration tasks as delegated by the supervisor.• Ensure Validation & Stability Manager/QC Lab Manager are informed of any potential delays or problems.• Complete and review Stability Studies within required timeframes to meet business needs.• Escalate non-resolvable technical/quality issues to management.• Assist with training of laboratory staff and support other laboratory areas, including calibration and cleaning responsibilities.• Gain experience using HPLC, GC, or AA.• Maintain the laboratory to cGMP standards and ensure readiness for audits.• Provide support in executing validation tasks and project paperwork.• Perform other tasks as assigned by the Validation & Stability Manager.Qualifications:• Degree in Chemistry, Biochemistry, or related field.• Experience in analytical testing within a cGMP/GLP environment.• Strong understanding of stability testing and quality control procedures.• Proficiency with laboratory instrumentation and troubleshooting techniques.• Excellent documentation and communication skills.• Ability to work collaboratively in a team and independently manage tasks.• Experience with HPLC, GC, or AA is a plus.