INTERN

Key Responsibilities

1. Process Support

• Assist in monitoring and documenting manufacturing processes for products under commercial or development stages.
• Support execution of process validation and verification activities.
• Participate in troubleshooting exercises under supervision.

2. Technology Transfer

• Support preparation of documents required for technology transfer.
• Assist in data collection, compiling process parameters, and preparing reports.

3. Data Analysis

• Collect, analyze, and interpret manufacturing batch data.
• Support trend monitoring, OOT/OOS evaluation, and basic statistical analysis.

4. Documentation

• Prepare and update SOPs, technical protocols, and reports.
• Maintain logs, batch records, and MSAT documentation as per GDP standards.

5. Cross-Functional Coordination

• Collaborate with Production, Quality, Engineering, and R&D teams for ongoing MSAT projects.
• Support scale-up or optimization projects under guidance.

6. Compliance

• Follow Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Ensure compliance with company policies, safety norms, and regulatory expectations.

Skills & Competencies Required

• Basic understanding of pharmaceutical manufacturing processes (solid dosage / injectables / biologics – as applicable).
• Strong analytical and problem‑solving skills.
• Good communication and documentation abilities.
• Proficiency in MS Office (Excel, Word, PowerPoint).
• Ability to work collaboratively in a team environment.

Education Qualification

• B.Pharm / M.Pharm
• B.Tech / M.Tech (Biotechnology, Chemical Engineering, Pharmaceutical Technology)
• M.Sc (Chemistry / Biotechnology)
• Freshers or final-year students eligible for internship