LSC have a great contract opportunity for an Associate Quality Control to join a South Dublin-based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 3+ 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:
- Participating in process engineering activities
- Facilitate the development of new business SOPs, Forms, Manuals, etc. using new processes/workflows
- Participate in system requirement, software configuration, and design activities
- Receive and/or verify master data for the site(s)
- Coordinate ELN Template development and review with site SMEs
- Support the development and review of Operational Qualifications
- Execute User Acceptance Testing & Data Migration Verification
- Review and provide input on training materials
- Support training material development by providing input and reviews
- Support site Instrument Qualification activities such as planning and execution
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's degree and 3 years of industry Quality Control or Quality experience
- GxP experience, specifically practices and requirements in the testing of biopharmaceuticals.
- Experience in development and validation testing of software used in a GMP environment.
- Experience and knowledge in using electronic lab notebook systems
- Experience in the use of other industry systems such as Veeva & Empower.
- Experience in testing or with processes involving analytical methods.
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 4777 329 if you have any more questions about this opportunity!
