LSC have a great contract opportunity for a QC Equipment Associate 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 working in the pharmaceutical or biotechnology industry ideally within QC and are ready for your next challenge, this could be the perfect project for you!
Key Responsibilities include
- Planning and conducting routine calibration, requalification and maintenance of laboratory equipment ensuring calibration and maintenance schedules are adhered to as per CMMS Maximo. Reviewing & filing of QC calibration & maintenance documentation
- Planning, executing and documenting the qualification of new laboratory equipment in a cGMP regulated environment, including the writing of equipment validation protocols and associated summary reports
- Conduct periodic reviews of instrument validation as part of validation life cycle
- Alerting Quality Control Management in the event of equipment failing to meet calibration or qualification requirements and conducting impact assessments/investigations as required.
Knowledge and Experience
- Bachelor's degree in a Science related field is required.
- Minimum of 3 years of laboratory experience in a cGMP laboratory environment including exposure to analytical instrument validation and data integrity assessments.
- Detailed knowledge of the methodology, and instrumentation and analytical techniques used for biopharmaceutical testing.
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 Grainne Hodnett on 021 4777 329 if you have any more questions about this opportunity!
