QA Validation Manager required for BioPharma manufacturing facility in Limerick. Will manage team of Validation Specialists - cleaning validation & SIP validation specialists.
- Manage, develop and build a team of subject matter experts in the areas of cleaning validation and SIP validation and continuing validation.
- Day to day management of resources, planning and assigning work to Validations Specialists and/or contingent workers to meet goals and deadlines.
- Ability to lead multiple and sophisticated validation programs, provide status reports and coordinating with other departments or outside contractors/vendors to complete validation tasks
- Lead technical and quality investigations.
- Collaborates with functional departments to resolve issues
- BS/BA in Engineering, Chemistry, or Life Sciences with 7+ years of related experience (may substitute relevant experience for education).
- Previous people management experience essential.
- Previous cleaning validation and steam in place experience an advantage.
- Understanding of Biopharmaceutical Drug Substance manufacturing process an advantage.