QC Lead, Ceredigion, West Wales
Pharmaceutical industry
£38,000 p/a
Up to 20% annual bonus + private healthcare etc.
THE ROLE…
- Perform routine duties as required in the analytical laboratory section in order to ensure the timely generation of accurate data and information.
- To lead the QCA function to ensure the timely generation of valid test results for the purpose of controlled product manufacture.
- To lead the sampling and testing of raw materials, process intermediates, and finished products, such that valid results are generated in a timely manner, inclusive of stability testing
- Maintain and develop state of the art knowledge applicable to existing and future processes and maintain up-to-date knowledge on regulatory expectations.
- To oversee the work, training and progression of employees within the QCA department.
- To ensure QCA activities follow standard operating procedures and are performed in compliance with GMP.
- To manage the investigation of out of specification results and incidents and to supervise and participate in the completion of any actions arising.
- To maintain all relevant documentation accurately, correctly and up to date.
- To perform, lead and assign project work as required
- Be responsible for: Senior Scientists, Scientists and Associate Scientists as designated
WHAT YOU WILL NEED…
- Educated to degree level in an appropriate scientific discipline.
- Significant experience in a biopharmaceutical or closely related industry.
- Computer literate.
- Strong technical background with an excellent working knowledge of GMP, Quality and Regulatory understanding
BENEFITS…
Private healthcare etc.
Work in a beautiful location – close to the countryside & coast
Join a friendly, collaborative team
IND123
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