Pharmaceutical Science Job at PI Health Sciences | Apply Now for Scientist Position
PI Health Sciences Ltd. is hiring an experienced Analytical Scientist to join its R&D team in Jaipur, Rajasthan. This Pharmaceutical Science Job requires candidates with an M.Sc. in Analytical Chemistry or Pharmaceutical Sciences and 3-5 years of experience in method development, validation, and transfer for raw materials and finished products. The successful candidate will leverage expertise in sophisticated techniques (HPLC, UPLC, GC) to conduct forced degradation, stability studies, and prepare critical technical documents compliant with global regulatory guidelines (ICH, USP, EP, JP).
About The Company
PI Health Sciences Ltd is presumed to be a dynamic organization operating within the highly regulated healthcare and pharmaceutical sector, potentially functioning as a Contract Development and Manufacturing Organization (CDMO) or part of an integrated pharmaceutical company. The company focuses on developing and delivering health science solutions, requiring strong expertise in analytical R&D, process development, and strict adherence to global regulatory standards like ICH, GMP, and GLP. Their scientific teams are crucial in supporting the development, validation, and stability testing of pharmaceuticals and intermediates to ensure quality and regulatory submission readiness.
About the Scientist Job
Qualifications & Experience:
- M.Sc. in Pharmaceutical Sciences, or a related field.
- 3-5 years of experience in analytical R&D within a CDMO, pharmaceutical, or biotechnology company.
Key Responsibilities of the Scientist Job
- Develop, validate, and transfer analytical methods for raw materials, intermediates, and finished products in compliance with regulatory guidelines (ICH, USP, EP, JP, etc.).
- Perform method development using techniques such as HPLC, UPLC, GC, MS, FTIR, UV-Vis, and dissolution testing.
- Support formulation development by providing analytical data for stability, compatibility, and process optimization studies.
- Troubleshoot analytical methods and instrumentation to ensure data integrity and reliability.
- Conduct forced degradation and stability studies to establish product shelf life.
- Prepare and review technical documents, including protocols, reports, SOPs, and regulatory submissions (IND, NDA, ANDA, DMF).
- Collaborate with R&D, quality control, and regulatory teams to support drug development projects.
- Maintain compliance with GMP/GLP and other regulatory requirements during method development and validation.
- Stay updated with advancements in analytical technologies and regulatory changes to enhance laboratory capabilities.
