Senior Compliance Manager – South East
Hartley People
- Munster
- Permanent
- Full-time
- Drive and implement site wide quality system improvements.
- Review GMP documentation written by colleagues to ensure all requirements are covered.
- Technical writing & execution of validation documents including Computer system validation
- Perform quality audits internally and for clients.
- Auditing of sites including WDA and MIA sites.
- Involved with Temperature and RH Mapping and preparation of associated documentation.
- 5+ years in a similar role.
- Knowledge of GMP/GDP is essential with industry experience.
- Experience in planning, scheduling, executing and leading audits preferable.
- Experience working within a pharmaceutical manufacturing environment in a Quality capacity.
- Experience managing teams and driving performance and change essential.
- Working knowledge of EU and US regulatory requirements.
- Experience acting as RP, desirable but not essential.