- Qualification of utilities like HVAC, Process and Purified Water system, and Compressed air system for Solid oral dosage forms (Tablets and Capsules).
- Conduct process validation, cleaning validation, deviation management, and SOP preparation.
- Qualification of manufacturing Equipment for Solid oral dosage forms (Tablets and Capsules).
- Requalification of equipments, utilities and facilities.
- Ensure compliance to the VMP planner for the requalification of the equipments and utilities.
- Ensure timely submission of regulatory documents and maintain accurate records.
- Collaborate with cross-functional teams to resolve quality issues related to formulation development.
- Prepare dossiers for product registration and variations, including CTD/eCTD submissions.
- Implementation of CAPA including effectiveness check plans
- Review and approve artworks.
📌 QA RA Manager (Vadodara)
🏢 Amico Formulations
📍 Vadodara
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.