Pharmaceutical Quality Control Specialist
4 weeks ago
Job Description:
CK Group are recruiting for a QC Chemist to join a company in the pharmaceutical industry at their site in Worthing, on a contract basis for 11 months. The successful candidate will be responsible for testing routine production and stability samples, calibrating and maintaining analytical equipment, and carrying out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a range of analytical techniques.
Key Responsibilities:
- To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets.
- Calibrate and maintain analytical equipment.
- Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (e.g. HPLC, Karl Fischer, dissolutions etc).
- To check and verify analytical testing and data generated by other analysts.
- To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date.
Your Background:
- A high standard and appreciation of GMP/GLP.
- Good reporting and recording skills using Standard Operating Procedures (SOPs) and site systems.
- Computer literate.
- Good communication and interpersonal skills, combined with flexibility.
- Good team worker.
Company:
Our client is a global healthcare company researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around £1bn in research and development in the UK annually.
Location:
This role is based at our client's site in Worthing.
Requirements:
It is essential that applicants hold entitlement to work in the UK. Please note that this role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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