Location – Macclesfield, UK
Hybrid Working - Min 3 days per week in HQ
Duration – 12 months
Inside IR35
Make a more meaningful impact to patients’ lives around the globe
In this role you will be 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. In addition, you will support the delivery of QA activities for their assigned portfolio of projects and provide advice to support the development, implementation and continuous improvement of GMP quality systems across the development functions and support implementation of agreed global standards.
Qualifications:
1. Appropriate scientific degree with experience (2-3 years) of working within a pharmaceutical GMP/ GCP environment, preferably within a pharmaceutical development organisation.
2. A broad understanding of Quality Systems and GMP is essential.
3. An understanding of the pharmaceutical/drug development process.
4. Preferable to have experience in Change Controls/ Deviations/ Batch Release.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.
Seniority level
* Associate
Employment type
* Temporary
Job function
* Project Management and Quality Assurance
* Pharmaceutical Manufacturing and Biotechnology Research
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