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LönHobson Prior are partnering with a brilliant pharmaceutical organisation on a contract basis. The opening position that is currently available is for a Specialist QA. Our client is focused on offering treatments that are much needed to those who need it.
Please note that to be considered for this role you must have the right to work in this location.
Key Responsibilities:
- You will offer quality advice to assist the development, execution and continuous improvement of GMP quality systems across the Clinical Supply function.
- Offering quality contribution to manufacturing, packaging, labelling & distribution actions.
- For this role, you will be accountable for quality release of manufactured drug product, investigational medicinal product for clinical trials.
- Any other assigned duties.
Requirements:
- Educated to a degree level in a pharmacy or engineering field, specialising in Pharmaceuticals.
- Demonstrable experience of working within a pharmaceutical GMP setting.
- Comprehension of Quality Systems and GMP and connected actions to Investigational Medicinal Product (IMP).
- Fluency in the English language.
- Communication skills both verbally and in writing.
- Familiarity with documentation, deviations, changes, and any other quality and compliance decisions in the development projects.
Apply now:
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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