Onsite QA Associate - GMP, CAPA & Compliance

Morgan McKinley; Limerick; On-site; EUR 60,000 - 90,000; Full time

Job summary

Morgan McKinley is seeking a QA Specialist (Assoc/Specialist/Sr Specialist) for a 12-month rolling contract in Limerick, onsite at a pharmaceutical site. The role ensures QA compliance across manufacturing, QC, validation, and facilities while supporting CAPA, investigations, and audits.

Education paths include Assoc Specialist, Specialist with 2+ years, and Sr Specialist with 5+ years (or MS 4+ years) in pharma or related fields.

Qualifications

• BS/BA in a scientific discipline or related field or equivalent.
• 2+ years pharma/related experience for Specialist level.
• 5+ years or MS 4+ years for Sr Specialist level.

Responsibilities

• Maintain site quality compliance across manufacturing, QC, validation, and facilities.
• Ensure cGMP regulatory compliance and review SOPs and CAPAs.
• Lead investigations, CAPA, and root cause analyses when needed.
• Support internal, regulatory, and customer audits.
• Provide quality system training and participate in continuous improvement.

Education

Assoc Specialist - BS/BA in scientific discipline or related field or equivalent combination of education and experience

Specialist - BS/BA in scientific discipline or related field with 2+ years of relevant work experience

Sr Specialist - BS/BA in scientific discipline or related field with 5+ years or MS 4+ years of relevant work experience

Job description

Morgan McKinley is seeking a QA Specialist (Assoc/Specialist/Sr Specialist) for a 12-month rolling contract in Limerick, onsite at a pharmaceutical site. The role ensures QA compliance across manufacturing, QC, validation, and facilities while supporting CAPA, investigations, and audits.

Education paths include Assoc Specialist, Specialist with 2+ years, and Sr Specialist with 5+ years (or MS 4+ years) in pharma or related fields.