Sigmar recruitment are looking for a QC Analyst for a market leader in the bio-pharmaceutical industry.
As a Quality Control Analyst, your mains duties will be:
- The QC Analyst will be responsible for one or more of the following activities in QC including analytical testing, characterization, method development, sample and data management and equipment maintenance.
- With a high degree of technical flexibility, work across diverse areas within the lab
- Plan and perform routine analyses with efficiency and accuracy.
- Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
- Report, evaluate, back-up/archive, trend and approve analytical data.
- Troubleshoot, solve problems and communicate with stakeholders.
- Initiate and/or implement changes in controlled documents.
- Participate in audits, initiatives, and projects that may be departmental or organizational in scope.
- Write protocols and perform assay validation and equipment qualification/ verification.
- Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
- Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.
- Bachelor’s degree in a science discipline.
- 1-2 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
- Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning
- Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery
- Experience with regulatory compliance in GMP manufacturing and testing of pharmaceutical products.
- Project Management and organizational skills, including ability to follow assignments through to completion
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