QA Resources is currently recruiting for a QA / Quality Specialist on behalf of a leading pharmaceutical company based in Cork. This is an initial 3-month project specific contract role.
Job Summary:
The QA / Quality Specialist will be part of a project team responsible for reviewing batch release documentation.
Responsibilities:
* Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records
* Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures
Education and Experience:
* Degree in Science, Quality, or a related Technical field.
* Experience in GMP Manufacturing or Quality Assurance environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing operations.
* Strong experience with documentation review
* Strong written and verbal communication skills
Interested candidates should submit an updated CV.
Please click the link below to apply, call Kellie on or alternatively send an up to date CV to
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***