Quality Specialist
- East
- Contract
- Compliance / Quality Assurance
This vacancy has now expired
Due to increase demand, they are expanding their team and require two Quality Specialists to join their team.
Responsibilities:
- Involved in supporting the global GMP Quality Assurance activities for the IMP Licence
- Complete auditing/ review of batch documentation to ensure compliance to SOPs, GMPs and applicable regulations
- Manage product recalls and stock recoveries as appropriate.
- Identify compliance gaps and make recommendations for continuous improvement
- Perform and review complaints and deviation investigations, change controls and CAPA’s.
- At least three years’ experience within the pharmaceutical industry
- A degree in a Quality, Science or Engineering discipline
- Knowledge of QA and compliance within a GMP manufacturing environment.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta Consultancy Services does not sponsor Visa applications.
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Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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