Granules India Limited is a globally recognized pharmaceutical manufacturing company with a strong presence in APIs, finished dosages, and healthcare products. Certified as a Great Place to Work® (2025-2026), Granules is known for its innovation-driven culture and commitment to quality in regulated markets like the US, EU, and Canada. With state-of-the-art R&D facilities in Hyderabad (Pragathi Nagar, Shamirpet & Gagillapur), the company offers excellent career growth opportunities for professionals in the pharma sector.
Job Description
We are seeking an experienced Formulation R&D Scientist specializing in solid oral dosage forms for regulated markets.
Key Responsibilities:
- Lead formulation and process development for US/EU/CA-compliant products, including NCE-1, F2F, or 505(b)(2) projects (oncology experience preferred).
- Design and execute QbD-based formulation strategies, from pre-formulation trials to pilot BE batches.
- Collaborate with cross-functional teams (Analytical, Regulatory, Production) for seamless project execution.
- Prepare technology transfer documents, stability reports, and product development reports with strict compliance.
- Ensure scalable product development and support manufacturing site technology transfers.
Eligibility Criteria
- Education: M Pharma (Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy).
- Experience: 7-10 years in formulation R&D for solid oral dosages (regulated markets).
- Skills: Expertise in QbD principles, bio-study evaluation, and regulatory documentation.
- Location: Hyderabad (Pragathi Nagar/Shamirpet/Gagillapur).
How to Apply
Interested candidates can email their updated resume to:
Email: praveen.kunchapudi@granulesindia.com
Website: www.granulesindia.com
Note: Only shortlisted candidates will be contacted.
