LSC have a great contract opportunity for a QMS QA Specialist to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra-rare disorders through the innovation, development, and commercialization of life-transforming therapeutic products.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Support key stakeholders during the preparation and management of audits/inspections.
- Support the development of the schedule / plan and its communication.
- Lead the creation of audit agendas by adequate identification of risks/issues and engagement with stakeholders to develop the audit.
- Review and approval of audit reports and issuance.
- Input data/feedback from report/response entry into the Quality Management system and tools.
- Lead the review of audit actions from receipt to closure.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Minimum of 5 years' experience in a GxP Quality Assurance or Compliance Management related role, with Quality Management Systems knowledge.
- Clear understanding of the audit lifecycle, from planning, conduct to closure.
- Demonstrable communication and project management skills; experience working in cross-functional teams.
For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available at this time. Thank you for your attention.
Apply via this advert or contact Gráinne Hodnett at LSC on 021-4777329 if you have any more questions about this.
