Freshers BPharma Job Vacancies at Revinto Life Science, Apply on Rasayanika
Job Title: Executive / Senior Research Associate – Formulation R&D
Location: Karwar, Karnataka
Industry: Pharmaceutical & Life Sciences
Functional Area: Research & Development (R&D)
Qualification: B.Pharma / M.Pharma
Experience: 0-1
CTC: As per industry standards and candidate suitability.
About Revinto Life Science
Revinto Life Science Private Limited, formerly known as Prakruti Remedies Pvt. Ltd., is a pharmaceutical and wellness company headquartered in Karwar, Karnataka. Established in 2003, Revinto focuses on the development and manufacturing of herbaceuticals, cosmeceuticals, nutraceuticals, and Ayurvedic formulations. With ISO 9001:2015 and GMP certifications, the company blends traditional knowledge with modern science to deliver high-quality, affordable healthcare solutions.
Job Overview:
We are seeking a dynamic and detail-oriented professional to join our Formulation & Development (F&D) team, specializing in Oral Solid Dosage, Oral Liquid Dosage, Topical Semisolid, and Nutraceutical forms. The role involves hands-on formulation development, pre-formulation studies, process validation, technology transfer, and stability studies while ensuring regulatory compliance with ICH guidelines and internal SOPs.
Key Responsibilities:
1. Literature Survey & Research
● Conduct comprehensive literature reviews to support new product development.
● Evaluate reference products, patents, regulatory data, and formulation strategies.
2. Pre-Formulation Studies
● Perform physicochemical characterization of APIs and excipients.
● Assess compatibility, solubility, and stability to support formulation design.
3. Formulation Development
● Design and optimize robust formulations across dosage forms.
● Conduct lab-scale and pilot-scale trials for process optimization.
4. Stability Studies
● Plan and execute stability studies in accordance with ICH guidelines.
● Analyze data and recommend formulation/process modifications as required.
5. Process Validation
● Coordinate and conduct process validation batches in production.
● Ensure adherence to GMP and internal validation protocols.
6. Technology Transfer
● Prepare and review Technology Transfer Documents (TTD).
● Support scale-up and successful handover of formulations to manufacturing teams.
7. Troubleshooting & Technical Support
● Provide technical assistance for ongoing production and post-commercialization issues.
8. Documentation & Compliance
● Maintain and update Product Development Files (PDF), logbooks, and other records.
● Draft and review documents such as MFRs, QAQN, and Finished Product Specifications (FPS).
9. Cross-Functional Coordination
● Collaborate with QC, QA, Production, and Procurement teams for smooth project execution.
● Report daily progress to the R&D Manager or Head of Department.
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