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:
- The successful candidate will proactively engage with all stakeholders involved with product quality.
- The QA Specialist is a member of the Global Quality Organisation who is a quality liaison between Global Product Development (US Based) , Manufacturing Operations, Quality Control, and Quality Assurance (US and Ireland) to ensure QMS and regulatory compliance.
- The role enables efficient communication and compliance for medical devices and combination products.
- Provides Quality Assurance support to an assigned area.
- Non-supervisory, provides advice in areas of processes and procedures.
- Role holder ensures efficient processes and procedures are maintained within the boundaries of regulatory compliance for relevant GxP.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's degree in a science discipline
- 3-4 years of experience in a similar role.
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.
