Alembic Pharmaceuticals is inviting applications for the position of Research Associate – Technology Transfer (OSD) at its formulation manufacturing facilities. This opportunity is ideal for M.Pharm graduates with 1–5 years of experience in technology transfer, MS&T, or formulation manufacturing who want to build a career in pharmaceutical product commercialization and scale-up.

With over 100 years of excellence in healthcare, Alembic Pharmaceuticals is known for its strong presence in global pharmaceutical markets and advanced formulation manufacturing capabilities. The company is looking for professionals experienced in technology transfer, process scale-up, and regulatory documentation for oral solid dosage (OSD) products.

This pharma job opportunity in technology transfer offers exposure to product development documentation, process optimization, regulatory support, and new product introduction at commercial manufacturing sites.

Job Details

• Position: Research Associate – Technology Transfer (OSD)
• Department: MS&T / Technology Transfer
• Qualification: M.Pharm
• Experience: 1–5 Years
• Industry: Pharmaceutical Manufacturing
• Company: Alembic Pharmaceuticals
• Job Type: Full-Time

Key Responsibilities

The selected candidate will be responsible for managing technology transfer activities for oral solid dosage formulations, ensuring successful scale-up and regulatory compliance.

1. Technology Transfer Documentation

• Review and provide technical inputs for Product Development Reports (PDR)
• Evaluate Master Formula Cards (MFC) and Technology Transfer (TT) documents
• Ensure documentation aligns with manufacturing and regulatory standards

2. Process Development & Scale-Up

• Prepare process risk assessments and protocols for feasibility trials
• Execute trial batches and scale-up batches
• Prepare technical summary reports for scale-up activities

3. Batch Documentation

• Prepare and review:
  • Exhibit batches
  • Batch Manufacturing Records (BMR)
  • Batch Packaging Records (BPR)

4. Regulatory Support

• Provide documentation support for regulatory submissions including:
  • Test License
  • Import License
  • No Objection Certificate (NOC)
  • Manufacturing License

5. Product Quality & Review

• Review Critical Process Parameters (CPPs)
• Evaluate Critical Quality Attributes (CQAs)
• Support Annual Product Review (APR) activities

6. New Product Introduction (NPI)

• Initiate and support NPI activities at manufacturing sites
• Ensure seamless transfer from R&D to commercial production

7. Process Improvement

• Implement Process Analytical Technology (PAT) for manufacturing optimization
• Support continuous process improvement initiatives

8. Documentation & SOPs

• Prepare and maintain Standard Operating Procedures (SOPs)
• Ensure compliance with GMP and regulatory guidelines

Required Qualifications

Candidates applying for the Alembic Research Associate Technology Transfer job must meet the following criteria:

• M.Pharm (Pharmaceutics / Industrial Pharmacy preferred)
• 1–5 years of experience in Technology Transfer or MS&T
• Experience in oral solid dosage (OSD) manufacturing
• Strong knowledge of GMP documentation and regulatory requirements
• Familiarity with BMR, BPR, PDR, and process scale-up activities

Skills Preferred

• Technology transfer and scale-up expertise
• Process validation and risk assessment
• Pharmaceutical documentation and compliance
• Knowledge of PAT and process optimization tools
• Strong analytical and problem-solving abilities

Why Join Alembic Pharmaceuticals?

Working with Alembic offers exposure to global pharmaceutical manufacturing operations and advanced formulation technologies.

Benefits include:

• Opportunity to work with a leading pharmaceutical company
• Exposure to international regulatory standards
• Career growth in MS&T and technology transfer
• Hands-on experience in commercial manufacturing scale-up
• Competitive pharmaceutical industry salary

How to Apply

Interested candidates can apply by sending their updated resume.

Email: msnt@alembic.co.in