Executive R&D Formulation Development – at VARAV BIOGENESIS Pvt. Ltd. Apply Now!
Looking to advance your career in pharmaceutical research and development? VARAV BIOGENESIS PRIVATE LIMITED is hiring an Executive – R&D (Formulation Development) at its Kala Amb, Himachal Pradesh facility. If you have 2-3 years of experience in formulation development and expertise in technology transfer, regulatory documentation, and stability studies, this is your chance to join a WHO-GMP-compliant pharmaceutical company committed to innovation and excellence. Take the next step in your pharma R&D career—apply now!
About the Job
Job Title: Executive – Research and Development (Formulation Development)
Company: VARAV BIOGENESIS PRIVATE LIMITED
Location: Kala Amb, Himachal Pradesh
Experience: Minimum 2-3 Years in Pharmaceutical R&D (Formulation Development)
Basic Qualification: B.Pharm / M.Pharm (Pharmaceutical Sciences or related field)
Job Overview
Job Overview: We are hiring a highly motivated and experienced Executive – R&D (Formulation Development) to join our Research and Development team. The successful candidate will play a key role in formulation development and technology transfer, working across varied dosage forms while ensuring strict adherence to regulatory requirements.
Key Responsibilities
- Formulation Development:
- Design and conduct laboratory-scale formulation trials to optimize product performance.
- Evaluate and select suitable excipients and develop different dosage forms including tablets, capsules, liquids, and topicals.
- Conduct stability studies and compatibility tests to assess formulation robustness.
- Prepare and maintain essential technical documentation (Master Formula Records, Manufacturing Process Documents, Stability Protocols, and Development Reports).
- Ensure all formulation development processes comply with current regulatory guidelines.
- Technology Transfer:
- Transfer developed formulations and processes to the manufacturing unit for scale-up and commercialization.
- Provide technical support during process validation, troubleshooting, and commercial batch execution.
- Collaborate closely with Production, Quality Assurance (QA), and Quality Control (QC) teams to ensure seamless knowledge transfer.
- Regulatory Documentation:
- Compile and review high-quality development reports, process optimization documents, and stability summaries.
- Ensure full compliance with Good Laboratory Practices (GLP) and Good Documentation Practices (GDP).
Required Skills and Qualifications
- Educational Qualification: B.Pharm / M.Pharm (Pharmaceutical Sciences or related field)
- Minimum 2-3 years of hands-on experience in Pharmaceutical R&D (Formulation Development)
- Strong understanding of formulation development across oral solids, liquids, and topicals
- Knowledge of ICH guidelines, WHO-GMP standards, and other regulatory requirement
- Ability to independently perform pre-formulation studies, excipient compatibility assessments, and stability testing
- Strong technical writing and documentation skills
Preferred Attributes
- Familiarity with analytical techniques such as HPLC, UV Spectroscopy, and FTIR (preferred)
- Exposure to ANDA/NDA documentation (advantageous)
- Proactive mindset with strong problem-solving and troubleshooting abilities
- Detail-oriented and process-driven approach
Keywords: Executive, Research and Development, Formulation Development, Job Pharmaceutical R&D, VARAV BIOGENESIS PRIVATE LIMITED
