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The QC Analyst will be working on site in Dundee, on a contract basis for 6 months.
Key Responsibilities:
- Perform analytical testing of raw materials, product packaging and final product to support the release, stability and in process testing of materials for production or products for commercial use.
- Accurately follow relevant SOPs, performing all activities in accordance with cGMP requirements, reporting anomalies. Initiate and complete laboratory discrepancy events on time.
- Document test results to ensure completeness and accuracy per cGMP, keeping accurate documentation.
- Demonstrate hands-on knowledge of operating, maintenance and troubleshooting skills for HPLC instruments as well as quality / regulatory requirements pertinent to quality control environments / laboratories.
- Performing moderate to complex equipment / instrumentation troubleshooting.
- Contribute towards the development and revision of SOPs, investigations, the preparation laboratory investigation reports and implement corrective & preventative actions (CAPAs).
- Support departmental improvement projects related to release goals, the identification of root cause for investigations and the improvement of laboratory methods.
- Educated to degree level or equivalent in a relevant scientific discipline such as Chemistry or Biology.
- Experienced analytical chemist with experience in chromatographic (HPLC and or GC) techniques.
- Strong knowledge of GMP and Data integrity requirements in QC environments.
- Strong troubleshooting skills.
- Industry background in a Pharmaceutical, Laboratory or related environment.
- Ability to conduct Laboratory investigations.
- Experienced with chromatography systems & software such as Chromeleon Software.
It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
