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Your main responsibility will include testing intermediates, products and raw materials in line with demand and business requirements.
Job Summary:
- Follow approved methods and procedures in accordance with cGLP & GMP requirements.
- Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements.
- Ensure QC documents are complete, accurate and compliant with procedures or guidelines.
- Ensure that investigations are performed in timely manner in accordance with set procedures.
- Carry out minor analytical method development to improve analysis, including HPLC, GC, spectrophotometric techniques and titrations.
- Identify ways to improve reduction in turnaround times and reduce costs, whilst still adhering to corporate quality standards.
- Assist in coaching and developing other members of the team.
- Chemistry (or very closely aligned subject) degree with experience as an analyst in a fine chemical or pharmaceutical industry role. HPLC and GC experience.
- Experience of working in a GMP environment / method development experience / cleaning validation experience.
It is essential that applicants hold entitlement to work in the UK. Please quote job reference99234 in all correspondence.
