Job Reference: JO-2003-65082_1584716227
- Perform chemical and physical analysis of In Process Control samples
- Perform analytical techniques in the area of Chromatography (HPLC, GC, TLC), spectroscopic methods (IV, UV) and wet chemistry techniques;
- Assure the right communication channel with the production areas in order to give the best response to the requests;
- Meet all GMP requirements as well as the Safety, Environmental and Health Regulations.
- To maintain all laboratory notebooks, records, chromatograms to an acceptable GLP standard.
- To maintain good housekeeping and hygiene within the laboratory.
- To maintain and follow all relevant Standard Operating procedures.
- To calibrate and maintain designated laboratory instruments.
- To support the laboratory testing schedule in order to achieve an efficient QC system.
- To bring to the notice of the supervisor or manager any discrepancies, deviations or non-conformance's in testing or work practice.
- To follow up to date analytical practices with reference to specifications, regulations and industry standards.
- To adhere to any agreed internal laboratory rota tasks.
- Liaising with other departments in relation to QC dispatch/testing
- To liaise with external suppliers/vendors in relation to QC consumables
- BSc in Scientific discipline
- 3-5+ years minimum work experience in the pharmaceutical industry
- Pharmaceutical experience in a GMP regulated laboratory environment
- Good communications skills
- Flexibility is essential (willingness to work shift patterns as required by business needs)
- Proven ability to work on own initiative
- PC skills MS Word, Excel etc.
- Proven technical ability in laboratory systems.
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