Quality Specialist
- East
- Contract
- Compliance / Quality Assurance
This vacancy has now expired
Our Partner in the Tipperary area develops and supplies the active ingredients and final formulated product for a range of innovative medicines at its manufacturing and R&D facilities. The plant, which has been operating in Tipperary for over 40 years, exports to over 25 countries around the world with primary markets being Europe, USA and Japan.
Responsibilities:
- Complete auditing/ review of batch documentation to ensure compliance to SOPs, GMPs and applicable regulations.
- Perform and review complaints and deviation investigations, change controls and CAPA’s.
- Review and approve production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods.
- At least three years’ industry experience
- Previous experience as a quality specialist within a pharmaceutical manufacturing environment.
The candidate must have the rights to work in the location stated in the job advert.
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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
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
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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Marcin
I manage this role.