About the Job
We are seeking a Senior Associate QC to join our team at an award-winning Pharmaceutical organization in Dublin. This is an excellent opportunity for someone looking to work with a leading multinational who excels in their field.
The Senior Associate QC will work under minimal supervision, responsible for one or more of the following activities in QC including analytical testing in process, stability, and finished products. The ideal candidate will have in-depth HPLC experience with Empower Software, some protein concentration testing background, and strong GMP lab environment experience.
* Testing of in process, stability and finished product samples, including HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management.
* Review and authorisation of Lab Data
* Support Analytical Technical Transfer activity testing reports and documentation.
* Document review/updates when required.
* Equipment Calibration, Maintenance and Trouble Shooting.
* Method Validation/Verification.
* Training of QC Chemistry Laboratory colleagues.
* Laboratory Investigation support
* Laboratory Housekeeping and maintaining GMP standards.
* Assisting in regulatory audits.
Required Skills and Qualifications
To be successful in this role you will hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject. You will also have 5+ years relevant experience in a pharmaceutical/healthcare environment. Strong technical writing skills are essential. Additionally, you should be detail oriented, self-motivated with good troubleshooting and problem solving abilities. Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous.