LSC have a great contract opportunity for a QC Analyst to join a Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
If you have 3 years of experience working in the 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 release and stability testing for drug substance and drug product samples in accordance with approved methods and cGMP requirements.
- Perform routine data analysis and review results based on demonstrated assay proficiency.
- Accurately document all laboratory activities in approved systems, ensuring data integrity and compliance with ALCOA+ principles.
- Assist with updating, reviewing, and approving controlled documentation, including SOPs, protocols, and reports.
- Identify, investigate, and document Out?of?Specification (OOS), Out?of?Trend (OOT), and deviation events in line with quality systems.
- Support preparation, execution, and documentation of technical transfer, co?validation, and method lifecycle activities
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- The ideal candidate should hold a minimum of a BSc. in Biochemistry or related discipline.
- Previous experience in a regulated biopharmaceutical laboratory is preferred. HPLC/UPLC and Empower experience is preferred but not essential.
- The successful candidate must demonstrate an ability to work independently and recognize anomalous trends or results.
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 on 021 4777329 if you have any more questions about this role!
