LSC have a great contract opportunity for a QA Compliance Specialist to join a leading biotech company based in Dublin.
If you have 5+ years of experience and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Support the review and approval of site deviation and investigations reports.
- Support the site change management process.
- Support Regulatory and Compliance Inspections at the site as required
- Support for management of recalls as required
- Comply with MSD Global and regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
- Build a Quality culture that delivers unconstrained supply, Right First Time to our patients.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's degree (or higher) in Chemistry, Biology, Microbiology, Automation, Engineering, or equivalent.
- 5 years' experience in Quality Control, Quality Assurance or Pharmaceutical, Vaccine or Biological Operations or Technical Operations.
- Excellent knowledge of relevant Quality and Compliance Guidelines (cGMP, Auditing, Quality Management Systems, Quality Agreements, Regulatory Affairs, Training) and respective regulations.
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 Grainne Hodnett on 021 4777 329 if you have any more questions about this opportunity!
