Quality Assurance Specialist - Contract - Pharmaceutical - South West
A fantastic opportunity for a Quality Assurance Specialist for an initial 3-6 month full time contract.
This QA role involves being responsible for and exisiting portfolio of products.
You will be involved the refining of the proposed risk assessment methodology, coordination of data collection, review and assessment of data, and preparation of the overall Quality Risk Assessment reports. You will also be involved in the review and assessment of operational GMP documents.
To apply for this role you must have;
A University degree or equivalent qualification in Life Science subject
Experience of at least 10 years in the Pharmaceutical Industry, of which the majority has been gained in a Quality Assurance environment.
Experience in manufacturing activities (solid dosage forms).
Plus experience equivalent to EU Qualified Person preferred.
Previous experience of preparing GMP risk assessments taking into consideration multiple sources of information, including Marketing Authorisation commitments.
Excellent knowledge of major global GMP requirements,with specific focus on EU and Canadian GMP and product licensing requirements.
In addition to the opportunity of working for an innovative company, you will be rewarded with an excellent rate of pay, and additional on site facilities including a gym, and transport to and from the nearest train station.
Please contact me urgently to discuss this role further on 0121 6163466.
Keywords; quality assurance, QA, qualified person, QP, GMP, solid dosage, validation, process, supply chain, manufacturing, pharmaceutical, south west, contract.Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.