Quality Assurance Specialist
2 weeks ago
CK Group are recruiting for a Quality Assurance Specialist to join a company in the Pharmaceutical industry at their site based in Macclesfield on a contract basis for 12 months. You will need to be on site for a minimum of 3 days a week.**Hourly/Daily Rate**:
£270 (Umb) / £250 (PAYE).
**Hours of Work**:
5 days / 36.5 hour a week.
**Essential Requirements**:
- It is essential that applicants hold entitlement to work in the UK.
**Quality Assurance Specialist Role**:
- Responsible for QA release of Drug Substance and Investigational Medicinal Product for clinical trials.
- Provide input to support of Packaging, Labelling & Distribution of IMP as required.
- Support the delivery of QA activities for their assigned portfolio of projects
- Provide advice to support the development, implementation and continuous improvement of GMP quality systems.
- Interpret, trend and report compliance data, to measure and improve quality standards.
**Background**:
- Appropriate scientific degree with experience (3-5 years) of working within a pharmaceutical GMP environment.
- A broad understanding of Quality Systems and GMP is essential.
- An understanding of the pharmaceutical/drug development process.
- A good understanding of batch release and batch review would be beneficial.
- A good communicator with experience of interacting effectively across interfaces.
**Company**:
Our client is a global research-based bio pharmaceutical company with a major UK presence who are committed to making a meaningful impact on people’s lives with life-changing medicines. This is a worldwide brand name which will not only look fantastic on yourCV for years to come but also offer inspiring and rewarding work.
**Location**:
This Quality Assurance Specialist will be based at our clients site in Macclesfield.
**Apply**:
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