Senior QA Consultant
- London
- Contract
- Compliance / Quality Assurance
This vacancy has now expired
Our client that specialises in producing radiopharmaceutical products for patients across the globe are currently seeking the expertise of an Senior QA Consultant
The successful candidate will be responsible for carrying out a re-fit of a clinical lab to transform it into a small GMP aseptic compounding manufacturing suite.
Essential Duties and Responsibilities for this Senior QA Consultant role include, but are not limited to, the following:
- Help deliver the new facility to QA GMP status and present to the MHRA to gain license.
- Implement a new manual paper-based QMS system
- Oversee quality procedures for validation plan etc.
- Help define, shape and action the strategy
- Facility design and qualification
- GMP/regulatory requirements to enable site license (MS Specials license)
- QMS design and implementation.
- Site validation plan construction and implementation
- Experience of helping to get a new site licensed
The candidate must have the rights to work in the location stated in the job advert.
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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
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
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