Role & responsibilities

Support the successful transfer of new products from R&D; to the manufacturing site. The role involves coordination of scale-up and exhibit batches, documentation preparation, technical support during execution, and collaboration with various departments to ensure timely and smooth product introduction and regulatory compliance.

Key Responsibilities

- Coordinate the transfer of products from R&D; to the manufacturing site.
- Review and finalize technology transfer documents from R&D; and external partners.
- Liaise with site teams to ensure readiness and approval of all TT documents.
- Identify and address technical gaps for smooth recent product introduction.
- Prepare and review batch records, protocols, and reports for scale-up batches.
- Monitor and provide technical support during execution of scale-up and exhibit batches.
- Support the regulatory team by providing required documentation for product filings.




- Ensure availability of all required materials (API, raw materials, packaging, consumables).
- Oversee sampling and stability testing as per approved protocols.
- Prepare and review SOPs; ensure compliance with cGMP guidelines.
- Assist production and quality teams during batch execution activities.
- Support Quality Management System (QMS) activities including deviations, CAPAs, and change controls.

Preferred candidate profile

- B.Pharm / M.Pharm / M.Sc. with 1-15 years in pharmaceutical manufacturing, Technology Transfer or MS&T;
- Experience in batch record preparation, production compounding, and IPQA batch monitoring.
- Familiarity with R&D; development activities.
- Strong cross-functional coordination and communication skills.
- Understanding of regulatory and GMP requirements.

📌 MSAT/Technology Transfer - Manager To Executive level (Hyderabad)
🏢 Anthea Pharma
📍 Hyderabad