LSC have a great opportunity for a QA Specialist to join a Cork Bio Project!
Our multinational Biotechnology client based in Cork are looking for QA Specialists to carry out tasks and projects related to managing compliance activities during qualification and validation related to projects as required by Good Manufacturing Practice (GMP).
In a team-based environment you will be trained to support QA activities for this Biopharma company.
If you’re interested in this role you should have the following experience and education:
o Bachelors Degree in a scientific/technical discipline required
o A minimum of 2 years’ experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry.
o Demonstrated knowledge and application of industry regulations as they apply to qualification and validation, including those of FDA, IMB, EMEA and other authorities
o Experience in statistical sampling plan development.
o Experience in a biopharmaceutical or pharmaceutical plant start-up.
Contact Regina Carroll at LSC for more details on 021-4777 329 or apply directly through this advert.