QA Specialist

A&C is delighted to announce that we’re hiring new staff at the A&C Bio Buffer’s manufacturing facility in Ireland, Co. Limerick.

We are currently looking for a Quality Assurance Specialist with at least 3 years of Quality Assurance experience or equivalent. Technical writing ability and knowledge of Pharmacopeial compendia, GMP, ICH and ISO guidelines are highly desirable.

Role description

The Quality Assurance Specialist participates in all Quality activities related to the business under the supervision of the Quality Manager. This role is responsible for maintaining the product specifications & certificate of analysis, raw materials release, work orders release, and other duties as required. He or she is required to be able to handle multiple tasks efficiently to ensure the quality activities that facilitate the production and customer requirements.

About A&C

A&C is a global GMP manufacturer of pharmaceutical excipients, buffers, process solutions and a select number of APIs. We have been servicing the life sciences industry since 1966 and we have sales offices and production facilities in various locations worldwide. A&C is a service-driven organization finding unique solutions to our customers’ GMP challenges. Our services include:

  • GMP custom ingredient development
  • GMP custom manufacturing
  • GMP custom packaging and repacking


We have two GMP manufacturing plants in North America and one GMP manufacturing facility in Ireland, Co. Limerick. The Irish facility (A&C Bio Buffer Ltd) is ISO 9001:2015 certified and is dedicated to GMP manufacturing of biological buffers, process solutions, cleaning solutions, chemical blends, WFI (water for injection) and GMP raw material repacking. A&C Bio Buffer is the only company in Ireland to manufacture biological buffers with water for injection.

A&C holds all the major quality certifications and applicable licenses from the main accreditation bodies and agencies, including ISO 9001:2015, EXCiPACT, DEL for manufacture of APIs, and Health Canada and FDA audited.

If you’re interested in this job opportunity, please send your CV to Shirley at or call 052 614 8880 for further information.

See the full job spec here



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