Highly Skilled Pharmaceutical Specialist
6 days ago
We are seeking a skilled Senior Associate Quality Control professional to join our team in Dublin. This is an excellent opportunity to work with a leading multinational company that excels in the pharmaceutical industry.
The ideal candidate will have experience with general test methods, including product sampling, and technical writing skills. They should also have experience planning and performing complex routine and non-routine methods and procedures, as well as conducting lab investigations in a biopharmaceutical or pharmaceutical industry.
Key Responsibilities:
- Plan and perform analyses with great efficiency and accuracy.
- Perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
- Report, evaluate, back-up/archive, trend and approve analytical data.
- Troubleshoot, solve problems and communicate with stakeholders.
- Implement changes in controlled documents.
- Participate in audits, initiatives and projects.
- Review protocols and perform assay validation and equipment qualification/ verifications when required.
- Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
- Contribute to regulatory filings.
- Evaluate lab practices for compliance on a continuous basis.
- Approve lab results.
- Interact with outside resources.
Requirements:
- Bachelor's degree in a Science related field.
- 3+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
- Strong technical writing skills (e.g. updating SOP) and investigation skills.
- Experience with analytical techniques such as Compendial testing would also be advantageous.
- Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
Location: Dublin, Ireland
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