5+

2-6 YEARS OF EXPERIENCE IN FINISHED GOODS, RAW MATERIAL and STABILITY. 2-5 YEARS OF EXPERIENCE IN MANUFACTURING GRANULATION, COMPRESSION and COATING and PACKING AREA

Oversees the development, implementation, and maintenance of the Quality Management System within the Probiotics or Non-Aseptic manufacturing facility. This includes ensuring that all processes, procedures, and documentation comply with relevant regulatory standards such as Good Manufacturing Practices.

Knowledge of Documentation, QMS, Deviation, Change Control, Market Complaint, OOS, OOT, Validation Qualification, IPQA, Audit Compliance.

Pre formulation studies of Pharmaceutical & Medicinal Devices and to check the compatibility of the API with different excipients. Formulation development of Pharmaceutical & Medicinal Devices. Execution of successful technology transfer at commercial site.

This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent will support the reference standard program within the Global Biologics department. The incumbent in this role will focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards.

Well-versed with QC related activities of Pharmaceutical Manufacturing Industry. Knowledge of CGMP & Safety Guidelines.

Sun Pharma is the fourth largest specialty generic pharmaceutical company in the world. We provide high- quality, affordable medicines trusted by healthcare professionals and patients in over 150 countries.

Ensure the on-time filing of high-quality regulatory submission, and to assist in the preparation, maintenance, and control of regulatory dossiers. Interact with Regulatory agency on regulatory submissions and follow up for drug product approvals.