QA Specialist – 12 Month FTC
AstraZeneca View all jobs
- Ireland
- Permanent
- Full-time
- Provide quality and cGMP oversight for all commercial manufacturing activities in the BDS facility.
- Review and approve executed and master batch records, including electronic batch record recipes.
- Review and approve technical documentation such as cleaning, process, and method validation.
- Review and approve SOPs, work instructions, technical reports, and protocols.
- Participate in and provide QA oversight for quality risk assessments.
- Support inspection readiness and engage directly with health authority inspectors.
- Oversee key QMS elements including deviations, change control, calibration, and preventive maintenance.
- Author, review, and approve quality procedures.
- Support supplier management activities.
- Review and release raw materials and components for manufacturing.
- Develop, track, and report quality metrics.
- Fluency in written and spoken English.
- Strong communication and presentation skills.
- Ability to work effectively in a complex, international matrix environment.
- Experience in the pharmaceutical or biotech industry.
- Strong leadership presence and the ability to influence cross‑functionally.
- Solid understanding of GMP, quality systems, and regulatory expectations.
- Degree in Pharmacy, Biology, Biotechnology, Engineering, or another relevant scientific discipline.