LSC have a great contract opportunity for a QC Material Management Specialist 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 2 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:
- Assisting with qualification of laboratory instruments.
- Participate in regulatory audits as required.
- Performing routine lab analysis, data analysis, assist in the investigation of OOS results, perform trending analysis and writing investigation reports and event reviews.
- Execute and assist in technical transfer and co-validation activities.
- Perform instrument performance checks and calibration.
- Participate in troubleshooting complex testing and instrumentation issues.
- Testing of materials/components to meet attainment and release metrics.
- Support the QC Laboratory with the testing and release of QC samples.
- Accurately documenting laboratory work adhering to best practice documentation behaviours and GMP level of quality.
- Complete peer review of documented lab results, logbooks, and associated documents to ensure testing has been completed in compliance with procedures.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- A degree in biological sciences, chemistry or related scientific disciplines.
- Experience in a lab-based role/ Quality Control / Sample Management role.
Apply via this advert or contact Jenny Murphy on 021 4777329 if you have any more questions about this role!
You will need to hold a Stamp 1G/Stamp 4 visa to apply. LSC do not provide work permit/visa sponsorship.
