LSC have a great opportunity for QA Specialist to join a South Dublin-based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 5+ years of experience in construction management/engineering within the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Act as disposition manager ensuring that batch disposition activities
- Manage and drive Quality records to closure including deviation records, investigation reports
- Initiate Quality records for supplier-related changes.
- Collaborate with Complaints team to request assessments, reviews complaint report and have comments addressed
- Provide data to the networks to support Quality Management Processes
- Take part in operational and quality improvement initiatives, programs, and projects.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- University degree. Engineering or Science related discipline preferred.
- Minimum of 4 years working in a cGMP manufacturing environment with a strong understanding of regulatory requirements and expectations.
- Ability to have a positive impact on others; the ability to affect the behaviors of others by connecting with and inspiring them
- Previous experience in batch release activities
- Good working knowledge of SAP.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship. Thank you for your understanding.
Apply via this advert or contact Gráinne Hodnett on 021 2067438 if you have any more questions about this opportunity!
