As a key member of our Pharmaceutical Quality Control team, you will play a vital role in ensuring the highest standards of quality and compliance. This is an exciting opportunity to work with a leading multinational organization based in Dublin.
* With technical flexibility, you will work across diverse areas within QC, planning and performing analyses with efficiency and accuracy.
* You will plan and perform multiple, complex routine/non-routine methods and procedures, as well as a large variety of assays.
* Responsibilities include reporting, evaluating, backing up/archive, trending and approving analytical data, as well as troubleshooting and communicating with stakeholders.
* You may train others as necessary, participate in audits, initiatives and projects, write protocols, and perform assay validation and equipment qualification/verification.
* Additional responsibilities include introducing new techniques to the lab, including method transfers, reports, validations and protocols, contributing to regulatory filings, conducting lab investigations, evaluating lab practices for compliance, and approving lab results.
For this position, we require a Bachelor's degree in a Science-related field and 5+ years of biopharmaceutical QC experience or related quality control/GMP laboratory experience in the pharmaceutical or medical device industry.
Additionally, you should have experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
If you are interested in this opportunity, please contact Rachel Kent at +353 (0)87 427 8808 or rachel.kent@lifescience.ie for further information.