Are you a pharmaceutical professional with hands-on experience in formulation development and product transfer? Arcolab is hiring for multiple positions in its Research & Development (R&D) division located in Bangalore. This is an excellent opportunity for candidates with 2 to 6 years of experience in formulation science, scale-up trials, and regulatory documentation to join a team focused on innovation and excellence in drug development.
🌐 About Arcolab
Arcolab is a respected name in the pharmaceutical industry, known for its commitment to developing high-quality, affordable medicines. With a strong focus on research and development, the company supports global healthcare needs through its advanced formulation capabilities and strategic partnerships with Contract Manufacturing Organisations (CMOs).
📍 Job Details
Position: Formulation Development – R&D
Location: Bangalore, India
Experience Required: 2–6 years
Employment Type: Full-Time
Department: Research & Development
🎯 Role Summary
The selected candidates will be responsible for managing various aspects of formulation development, including product transfers, feasibility trials, scale-up activities, and regulatory documentation. This role involves close coordination with internal teams and external CMOs to ensure smooth execution of development projects and compliance with quality standards.
🔍 Key Responsibilities
Review and understand product-related technical details from internal sites to facilitate seamless transfer to external CMOs.
Handle investigations related to OOS (Out of Specification), OOT (Out of Trend), and deviations for new products and site transfer projects.
Conduct feasibility trials and scale-up trials for new formulations.
Manage Product Robustness Projects, including trial execution, monitoring of optimisation batches, and registration/commercial batch activities.
Review critical documents such as Annual Product Quality Reviews (APQRs), Root Cause Investigations (RCIs), Corrective and Preventive Actions (CAPAs), and Product Development Reports (PDRs).
Prepare and review technical documents, including Master Formula Records (MFRs), Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), and trial protocols/reports.
Review and approve Product Validation Protocols (PVPs) and Product Validation Reports (PVRs).
🧠 Candidate Profile
Education:
Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, or a related field.
Experience:
2 to 6 years of relevant experience in formulation development, scale-up, and regulatory documentation.
Skills:
Strong understanding of pharmaceutical manufacturing processes.
Familiarity with regulatory requirements and documentation standards.
Ability to manage multiple projects and work collaboratively with cross-functional teams.
Attention to detail and problem-solving abilities.
📩 How to Apply
Interested candidates can share their profiles directly with the recruitment team at:
📢 Final Thoughts
This is a fantastic opportunity for mid-level professionals in the pharmaceutical industry to contribute to high-impact formulation projects. If you’re passionate about drug development and regulatory excellence, the Formulation Development roles at Arcolab in Bangalore could be your next career milestone.