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Providing expert temporary talent solutions for the life sciences industry, with a specialised focus on Quality Assurance and Technical Operations
GMP Quality Assurance Specialist II
Location: Ballydine, Co. Tipperary, Ireland
Work Structure: Monday – Friday, 39 hours per week
Looking to advance your career in Quality Assurance? Our client is seeking a GMP Quality Assurance Specialist II to join their team in Ballydine. This is a fantastic opportunity to gain hands-on experience in a dynamic pharmaceutical environment.
Why Apply?
* Competitive contract opportunity with a leading pharmaceutical company
* Hands-on experience in GMP and compliance activities
* Work within a supportive, collaborative team environment
Your Role
You’ll be responsible for key Quality Assurance activities, including:
* Reviewing and approving production and analytical documentation
* Supporting batch release, QP certification, and compliance activities
* Investigating deviations, complaints, and managing CAPAs
* Conducting internal audits and ensuring adherence to GMP requirements
* Collaborating with cross-functional teams to drive continuous improvement
What You’ll Need
* A degree in Science or Engineering (or relevant industry experience)
* Knowledge of GMP, regulatory requirements, and quality systems
* Experience in deviation investigations, CAPA management, and documentation
* Strong communication and problem-solving skills
This role offers a great opportunity for junior QA professionals to develop their expertise in an established pharmaceutical setting. Ready to take the next step? Apply today!
Please note: You must be able to work in the Ireland or the EU without restriction or sponsorship to be eligible for this role.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance and Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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