
Senior QC Analyst (Analytical Chemistry Team)
- Dún Laoghaire, Co Dublin
- Contract
- Full-time
- Plan and perform analyses with great efficiency and accuracy.
- Plan and 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.
- Initiate and/or implement changes in controlled documents.
- Participate in audits, initiatives and projects that may be departmental or organizational in scope.
- 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
- May conduct lab investigations as necessary.
- LIMS data coordination of commercial and import testing on site where applicable
- May represent the department/organization on various teams.
- Bachelor's degree in a Science related field is required.
- 2+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry,
- Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
- Have experience with analytical techniques such as Compendial testing as outlined above.
- Be very proficient in the use of Microsoft Word, Excel etc.
- Have strong communication and technical writing skills.
- Be detail oriented, self-motivated with good troubleshooting and problem-solving abilities.
- Be a self-starter and capable of working on own initiative.
- Strong teamwork skills.
- Proven track record of meeting deadlines.