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Quality Specialist

  1. Cork
County Cork
  1. Contract
Competitive
  1. Compliance / Quality Assurance
28104ZD

This vacancy has now expired

Quality Specialist - Documentation - Global Pharmaceutical Company - 11 month contract - Co. Cork

One of our global Pharmaceutical clients is looking for a Quality Specialist to join their team close to the picturesque and historical city of Cork. The site is renowned for manufacturing excellence and plays a vital role in the company's large-scale biotech operations worldwide. 

The site has received over $300 million investment over recent years in order to meet the demand for the company’s innovative products and will continue to evolve.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:
  • Responsible for the Site Documentation System including Issuance, reconciliation, storage, archiving and retrieval of cGMP documentation to support the manufacture & testing of our products.
  • Responsible for maintaining the Site Master file for current effective cGMP documents on site.
  • Uses knowledge to improve Quality Documentation Systems
Requirements:
  • At least one year’spharmaceutical industry experience.
  • cGMP documentation control SME knowledge, from both operational and educational experience, is required
If you are interested, please apply now for more information!!




The candidate must have the rights to work in the location stated in the job advert.

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