LSC have an exciting contract opportunity for QC Analyst to join a leading biotechnology company based in Dublin and make a real impact in the field of quality control.
The Sr Associate QC position is perfect for those who have 3+ years biopharmaceutical QC experience with product testing in a GMP laboratory setting..
ABOUT THE ROLE:
-
Perform a wide variety of assays, including routine and non-routine methods
- Evaluate and approve analytical data, ensuring compliance with cGMP standards
- Troubleshoot issues and communicate effectively with stakeholders
- Participate in audits, initiatives, and cross-functional projects
ARE YOUR SKILLS A MATCH:
- Bachelor's degree in a Science-related field
- 3+ years of biopharmaceutical QC experience or related GMP laboratory experience
- Experience with analytical techniques such as pH, clarity, and osmolality testing
- Detail-oriented with excellent problem-solving abilities
- Self-motivated and capable of working independently
- Proven track record of meeting deadlines and working effectively in a team
Apply today directly through this advert or contact Kathy Gillen on 021 47718212 for further information. All applicants must hold a valid work permit and visa for at a least 12 months. LSC cannot provide work permit sponsorship.
