The QC Analyst will be responsible for supporting site activities related to performing testing of Raw Materials, in-process samples and laboratory duties in accordance with cGMP regulations.
Responsibilities will include;
- Performing QC testing (TOC, Nitrates, Conductivity) of water samples. Performing analysis of Raw Materials including HPLC, GC, KF, UV, IR and wet chemistry techniques. Completion in a timely and accurate manner of laboratory documentation as directed by the QC Material Management Supervisor.
- Compliance with Standard Operating Procedures and Registered Specifications.
- Assisting in authoring and reviewing documentation, including SOPs, as required.
- Batch paperwork review, and reconciliation of analysis performed in laboratory. Ensuring that any out of specification results are investigated according to site procedures.
- Assisting with out of specification investigations and deviations using the Infinity system.
- Sample management activities- ensuring chain of custody is maintained using CIMS and LIMS.
- Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
- Performing any other activities as indicated by the Lab Supervisor.
Qualifications and Experience:
- The ideal candidate should hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline.
- 1 -2 years of experience in a pharmaceutical / healthcare laboratory or related technical function.
- Experienced in Water testing, HPLC, KF or FTIR an advantage.
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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