Company Jobs

Your function in ensuring data accuracy is critical. You’ll validate ingredient information and toxicological data to maintain consistency across products and platforms. You will connect these elements by adapting to the evolving landscape of consumer safety and seeking innovative ways to manage and communicate ingredient data.

Responsible for monitoring and ensuring quality of products and comply with cGMP standards. Monitoring of critical process parameters, line clearance before batch initiation, verification of RM and equipment. In process sampling for quality check like pH, moisture content, and reaction monitoring.

Pharma Graduate with 2-8 years of experience in tablet and Liquid sterile manufacturing and Production QMS. Track and Trace systems, Manufacturing, Compounding of Nasal Spray formulations, vial Washing and filling machines. Having Good experience on online documentation and Knowledge to work in GMP environment.

The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

Contribute to preparation including authoring where relevant and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and/or regional perspective.  Good understanding of regulatory guidelines, regulatory framework, including regional trends, for various types of applications and procedures.

RM, PM, FG, Dispensing, Dispatch, Documentation. After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

Candidate with project management experience in Discovery Sciences along with Commerical or Product launch, Product strategy experience would be preferred; should be adept at managing project milestones, budget and stakeholders.

Analysis and processing of In process and Finished product and handling of HPLC, UV, FTIR, K/F, AAS, IC, Dissolution. Analysis of Raw material and Excipients and handling of HPLC.

The candidate will be responsible for preparation and submission of dossiers for NCEs and NBEs and will present it to relevant internal and external stakeholders. The candidate will represent the company with Indian regulatory agencies, including CDSCO, RCGM, Central Bureau of Narcotics and Karnataka drugs control department.