Title: Senior Research Associate – Medak, Telangana, India
Location: Digwal, Medak, Telangana, India
Job Type: Full-Time
Category: R&D / Analytical Chemistry
Company Overview:
Piramal Pharma Solutions (PPS), a part of the Piramal Group, is a leading Contract Development and Manufacturing Organization (CDMO) providing end-to-end solutions across the drug lifecycle. With a globally integrated network of facilities across North America, Europe, and Asia, PPS offers services ranging from drug discovery, process development, clinical trial supply, API and finished dosage manufacturing, to specialized solutions including highly potent APIs, antibody-drug conjugates, peptides, and biologics. PPS combines technical expertise with ethical practices to support innovators and generic companies worldwide.
Role Overview:
We are seeking a Senior Research Associate to support Analytical R&D (AR&D) activities in compliance with GMP and safety standards. The role involves independent project handling, analytical method development, validation, routine analysis, and close collaboration with QC, QA, and safety teams.
Key Responsibilities:
Manage independent analytical projects and support PDG synthetic groups.
Conduct analytical method development, implementation, validation, and routine analysis.
Perform method transfer to QC, including preparation of method transfer protocols and reports.
Generate analytical documentation such as method development reports, validation reports, specifications, and standard test procedures.
Operate and maintain laboratory instruments, including HPLC, GC, potentiometers, and polarimeters.
Ensure API stability studies and maintain GLP practices in accordance with 21 CFR Part 11.
Calibrate instruments according to master calibration schedules and maintain online laboratory journals and instrument logbooks.
Ensure compliance with hazardous waste and chemical management protocols.
Maintain a clean, organized laboratory environment under controlled conditions.
Qualifications & Experience:
Education: M.Sc in Analytical Chemistry, Chemistry, or Organic Chemistry.
Experience: 4–8 years in API manufacturing and analytical testing under GMP.
Skills & Competencies:
Expertise in analytical method development, validation, and routine analysis.
Strong knowledge of API stability testing, GLP practices, and 21 CFR Part 11.
Proficiency in operating HPLC, GC, potentiometers, and polarimeters.
Excellent documentation skills, including preparation of protocols, reports, and SOPs.
Ability to work independently and coordinate with QA, QC, and SCM teams.
Strong attention to detail, safety awareness, and organizational skills.
Why Join Piramal Pharma Solutions:
Opportunity to work in a globally integrated CDMO with exposure to cutting-edge technologies.
Be part of a culture that values ethical practices, inclusive growth, and professional development.
Contribute to the development and manufacture of innovative APIs, peptides, biologics, and finished dosage forms.
Competitive salary and career growth in a leading pharmaceutical organization.
Equal Opportunity Employer:
Piramal Group is an equal employment opportunity and affirmative action employer. All employment decisions are made based on qualifications, skills, performance, and merit, without discrimination based on legally protected characteristics.
Apply Now: Join Piramal Pharma Solutions to advance your career in analytical R&D and pharmaceutical development, contributing to high-quality drug development and manufacturing on a global scale.
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