- Principal Quality Assurance Auditor (Home or Office Based UK)
To assist with the development and maintenance of audit programmes (internal and external) as part of the Quality Assurance program within the Pharm-Olam Group of companies. Responsible for scheduling and conducting study related audits to support Pharm-Olam/MBQ Sponsors
- EMEA Quality Assurance Director.
A global pharmaceutical with its HQ based in Basel, currently have a strong presence within the research and development of therapeutic solutions. They are looking...
- Quality Assurance Manager - Mid Sized Pharmaceutical Company
An outstanding career opportunity for an experienced quality assurance professional who is looking to move into a mid sized pharmaceutical company. As a QA Manager, you will be responsible for all activities related to Quality Assurance as well as ensuring that the company is in compliance with GMP regulations, corporate expectations and industry standards.
- PW 6046 Manager, Quality Assurance
This is an excellent opportunity for a QA Manager looking for an exciting challenge in this growing global pharma organisation. The role will be accountable for QA activities relating to the manufacture, packaging, testing, storage and distribution of investigational medicinal products ensuring compliance with current GMP, internal Quality Systems, Corporate expectations and Industry Standards.
- Quality Assurance - Supply Chain
This is an excellent opportunity to join an experienced pharmaceutical company as a Quality Assurance - Supply Chain Specialist based in the South-East of England. This is an organisation which has a 30-year track record of innovation and success in developing new drug delivery systems in addition these technologies have been successfully commercialised in multiple products around the globe. This is a 12 month contract role with the possibility of an extension. ...
- Principal GCP Auditor - UK Based
Pharm-Olam International (UK) are actively seeking an experienced QA Auditor with substantial experience in the GCP field. The ideal candidate will come from a CRO background with a minimum of 5 years experience working as a Clinical QA Auditor.
- Data & Quality Manager
Excellent opportunity for a Data & Quality Manager
- Senior Quality Engineer
Senior Quality Engineer, East Anglia, Global Pharmaceutical CompanyProcess Quality Engineer required for leading Pharmaceutical manufacturing company. You will work as part of the established QA Team. The work will largely be defined projects to support improvements in both process and production, you will also be responsible for the coordination of multiple investigations. This is a Permanent opportunity based in East Anglia, candidates must be eligible to work in the UK. ...
- QA / Documentation Specialist - Devices - Vienna
A specialist Medical Devices company that is a great client of mine and who are growing extremely fast, is looking for a Documentation specialist to join their site near the beautiful town of Vienna.
- EMEA Medical Devices Registration Manager
EMEA Medical Devices Registration Manager
Employment Type: Permanent
Our highly established client is currently seeking an experienced Product Registration Manager to join their Regulatory team as a European Product Manager. This is an exciting role promising you diversification and variation within your role.