Company Jobs

The incumbent would need to build a strong New Product Portfolio and its management and delivery in a time bound manner for India Business of Sun. Works closely with the Business/Marketing, Business Development, R&D, Manufacturing, Regulatory, IP, Market Research, SFE, CEO Office, Commercial, Medical, Clinical Research, CQA, Finance, PMO, New Product Launch, Network Strategy, Packaging development teams etc.

To develop approaches for Downstream processes, designing and managing multiple process development projects; to take up new technology initiatives within the downstream development group. To draft primary documents for functional deliverables.

As a CDC Trial Manager is the main accountable person in making sure that deliverables are met as per project timelines, within budget and complying with Protocol, country regulatory requirements, Helsinki Declaration, GCP, Good Clinical Practice, and NN SOPs Standard Operating Procedures. bachelor degree in life science, pharmacy, or nursing qualification or equivalent.

Provides critical support and coordination in the review of safety and regulatory publishing documents, ensuring timely and accurate processing upon receipt. Plays a key role in maintaining document quality by tracking safety and regulatory publishing data, ensuring seamless uploading into internal and/or external electronic trial master files.

Candidate must have an injectable background. Candidate must have knowledge of Software like Lab Solution, Chromeleon & Spectrum. Candidate must have knowledge of Instruments like UV, HPLC, FUR, GC, LPC, TOC, Polari meter, Refractometer.

As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. 

Successfully launch assigned brands in a specialty segment in line with brand strategy. Plan and consistently achieve patients on therapy, unit targets and value targets. B.Pharm / M.Pharm / M.Sc. candidates preferred.

Execute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target. Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement

Analytical Method Development, Method Validation, Analysis, HPLC, Stability, RM,GC, IP/FP