Analytical Scientist Role at PI Health Sciences | Apply Now for the Chemistry Jobs
Are you looking for a rewarding career as an Analytical Scientist in the pharmaceutical industry? PI Health Sciences Ltd is hiring in Jaipur, offering an excellent opportunity for professionals searching for Chemistry Jobs in analytical R&D. In this role, you will support drug development projects through method development, validation, stability studies, regulatory documentation, and collaboration with cross-functional teams.
About PI Health Sciences
PI Health Sciences Ltd is a leading CDMO offering advanced pharmaceutical research, development, and manufacturing solutions. The company provides cutting-edge analytical R&D services, making it an ideal place for Analytical Scientists seeking impactful Chemistry Jobs. With state-of-the-art laboratories, modern instrumentation, and a focus on global regulatory compliance, PI Health Sciences delivers high-quality, reliable results across formulation, stability, and method development projects. The organization fosters innovation, collaboration, and professional growth, offering diverse PI Health Sciences careers for talented professionals passionate about advancing healthcare through science, technology, and analytical excellence.
Job Details
- Job Title: Analytical Scientist
- Location: Jaipur, Rajasthan, India
- Qualifications: M.Sc. in Analytical Chemistry, Pharmaceutical Sciences, or a related field.
- Experience: 3-5 years of experience in analytical R&D within a CDMO, pharmaceutical, or biotechnology company.
Key Responsibilities:
- 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.
