Qa Specialist - Validation

Quality Assurance Specialist (Validation) Sligo Pharmaceutical/Biotechnology/Manufacturing **Job Summary:** We're seeking a dynamic **QA Specialist (Validation)** to ensure our products meet GMP and regulatory standards.
You'll play a key role in reviewing validation documents and overseeing facility, equipment, and utility qualifications.
This hands-on role supports start-up and ongoing manufacturing, while ensuring compliance with the Site Validation Master Plan.
**Key Responsibilities:** - Provide QA expertise for validation, new products, and manufacturing.
- Review and approve validation documents and equipment qualifications.
- Manage QMS areas (Deviation Investigations, Change Control, CAPA).
- Collaborate with cross-functional teams on continuous improvement initiatives.
**Requirements:** - Bachelor's in Science/Engineering.
- 5+ years in GMP QA, supporting validation activities.
- Strong knowledge of validation lifecycle, cGMP, and quality systems.