What are the responsibilities and job description for the Analytical Scientist - Method Development position at Porton Pharma Solutions Ltd.?
About the Role:
Porton Pharma Solutions Ltd. is seeking a highly skilled Research Scientist to join our Analytical R&D and QC department within the CDMO industry.
The ideal candidate will have a strong background in analytical chemistry and experience in method development, validation, and quality control testing.
- Conduct analytical method development and validation independently.
- Troubleshoot analytical methods as needed.
- Conduct release testing for GMP regulatory starting materials, intermediates, and final APIs.
- Participate in OOS and deviation investigations.
- Support Quality Assurance during internal audits and client audits.
Key Requirements:
- BS, MS, or PhD in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or a related field.
- 3 years of experience in analytical R&D and/or QC within the pharmaceutical or CDMO industry.
- Strong knowledge of analytical techniques, including HPLC, GC, UV-Vis spectroscopy, and dissolution testing.
