We have an exciting opportunity for a QA Specialist to join an expanding team with a pharmaceutical company in Cork to help support the Quality team.
Managing compliance activities and QA operational activities related to operational projects as required by Good Manufacturing Practice (GMP).
This person will be responsible for change control, non-conformance investigations, compliance auditing, and other related quality system elements.
Responsible for implementation of systems and procedures for the management of change control and deviation management, as it applies to plant installations, systems, and operations in accordance with GMP.
Quality oversight of project activities including but not limited to, C&Q activities and process validation through to commercial manufacture.
To Bachelors Degree in a scientific/technical discipline required
A minimum of 3 years experience in a quality or compliance role within the biological and/or pharmaceutical industry.
Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. Ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position.
If you believe this would be a good fit for you, or would like to find out more about this role and many more please click the 'apply now' button or reach out to Aisling Couch, Specialist Quality Consultant at MMK on 021 2300 300 or email@example.com.
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.