Job Description
Here is your chance to join a multinational pharmaceutical company on a permanent basis as they look to expand their QC team.
A fantastic opportunity to join a sucessful pharmaceutical company as they expand their quality control team.
Responsibilities:
1. Performing analysis of in-process, raw material, final product and stability samples
2. Interpreting the raw data and results generated, documenting and reporting as per written procedures and as per schedules in accordance with cGMP and all other regulatory requirements
3. On completion of analysis, performing independent data review of all analysis as per schedule. Reporting and documenting of results must be completed accurately and promptly and in accordance with cGMP and all other regulatory requirements
4. Sampling of raw materials & process /purified water
5. Carrying out the qualification, maintenance and calibration of QC Instrumentation as per schedules, ensuring relevant KPIs are met
6. Troubleshooting problems which occur when using instruments and implementing solutions to avoid re-occurrence
7. Supporting effective root cause analysis and timely closure of investigations
8. Improving laboratory RFT through use of effective root cause analysis and CAPA actions and improving analytical testing processes
9. Developing, revising and implementing procedures to comply with appropriate regulatory requirements
10. Executing instrument and method validation protocols in accordance with written procedures.
11. Supporting/participating in Analytical Method Transfer and other validation projects.
12. Working with management and staff to foster an ethos and culture of safety awareness, where safety is accepted as an integral part of the overall business
About you:
13. Minimum 2 years experience in a QC analyst postion or equivilant
14. Experience using Empower and Labware LIMS would be advantageous
15. Ability to makes suggestions for improvement, new initiatives, ways to minimise costs and challenges current ways of work to improve efficiency
16. Ability to coordinate and communicate effectively with the QC Leadership team
17. Thorough knowledge of GMP and regulatory requirements
18. Understanding and ability to perform audit preparation and inspection
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
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