Our client, a prominent player in the pharmaceutical industry, known for their commitment to producing high-quality medicines that improve and save lives, is currently seeking a dedicated and detail-oriented QC Analytical Data Specialist to join our quality control team in Switzerland.
Key Responsibilities:
- Review and evaluate analytical data, including HPLC, GC, dissolution, and other relevant methods.
- Ensure data accuracy, completeness, and compliance with established procedures and regulatory standards.
- Investigate and document any deviations or discrepancies in analytical results, initiating necessary corrective and preventive actions (CAPAs).
- Collaborate with the QC team and other departments to resolve data issues and discrepancies promptly.
- Maintain accurate and organized records of reviewed data and associated documentation.
- Support method validation, transfer, and development activities when required.
- Keep up-to-date with industry regulations and best practices related to analytical data review.
Qualifications:
- Bachelor's or Master's degree in a relevant scientific discipline.
- 5 years of experience in a pharmaceutical or biotechnology analytical laboratory.
- Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis, and dissolution.
- Familiarity with GMP, ICH, and FDA guidelines and regulations.
- Excellent attention to detail and the ability to identify data anomalies.
- Effective communication skills and a collaborative mindset.
Can this be interesting for you or anyone you know? If so, please apply here or contact Conor Kelly with your number/CV ASAP and he will give you a call.
?: +41 (0) 44 5514 407
?: c.kelly@panda-int.com