Analytical Scientist Job at PI Industries – Apply Now
Are you a highly experienced professional in Analytical Research & Development seeking a dynamic and growth-oriented career move? A renowned pharmaceutical and biotechnology company based in Hyderabad is inviting applications for the role of Analytical Scientist. This is a golden opportunity for professionals with 3–8 years of hands-on experience in analytical method development, validation, and regulatory documentation, especially within CDMO or pharma R&D environments.
If you hold a Master’s or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related discipline, and possess deep expertise in advanced techniques like HPLC, UPLC, GC, MS, FTIR, and UV-Vis, this role positions you at the forefront of innovative drug development. You’ll work closely with cross-functional teams in R&D, Regulatory Affairs, and Quality Control to drive high-impact projects that directly contribute to global healthcare solutions.
Whether you’re looking to expand your scientific capabilities, gain exposure to international regulatory standards, or be part of a company committed to technological advancement and patient-centric innovation, this role offers the perfect platform to elevate your career in pharmaceutical research.
Analytical Scientist
Hyderabad, Telangana, India ·
Qualifications & Experience:
Master’s or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related field.
3–8 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.).
- Develop methods 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.
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