LSC have a great contract opportunity for a QC Senior Analyst 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.
If you have 4 years of experience working in the biochemistry, pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Perform all lab functions in compliance with cGMP.
- Follow written procedures for the following tests, as trained and qualified:
- Gel electrophoresis (SDS-PAGE, IEF).
- ELISA and plate-based assays (potency and residual assays such as HCP and ProA).
- Stability scheduling and testing.
- Recognize and report aberrant test results and sample conditions.
- Provide QC SME and day to day technical guidance to QC biochemistry analysts.
- Lead and complete execution of investigations/CAPAs in a timely manner.
- Provide lab support including reagent preparation, cleaning, and routine equipment maintenance.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- BSc in Chemistry or a biological science
- 4-7 years' experience with experience in gel electrophoresis (SDS-PAGE, IEF), ELISA and plate-based assays
- A working knowledge of the cGMP QC laboratory environment, and equipment associated with testing of biopharmaceutical products.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Kathy Gillen at LSC on 021 4781212 if you have any more questions about this role!
