๐งช Cohance Life Sciences Jobs 2026 โ Regulatory Affairs Vacancy in Ankleshwar
๐ข Company: Cohance Life Sciences
๐ผ Position: Sr. Executive โ Regulatory Affairs
๐ Department: Regulatory Affairs
๐ Location: Ankleshwar, Gujarat
๐ Qualification: Any Science Graduate / Postgraduate
๐ผ Experience: 6+ Years
๐ญ Industry: API Manufacturing
๐ฌ Key Responsibilities
- ๐ Handle global API regulatory submissions
- ๐ Prepare and manage DMFs, CEPs, registration dossiers
- ๐ Manage DMF lifecycle, renewals, amendments and annual reports
- ๐ Prepare responses to regulatory queries and deficiencies
- ๐๏ธ Handle ODMF/APDMF and customer-specific regulatory documentation
- ๐ป Work with regulatory platforms such as PharmaReady, Lorenz eCTD Validator, EMA Portal, CESP, ESG Gateway and CDER NextGen Portal
- ๐ Support submissions for US, Europe, China, Brazil, Korea, Russia and other regulated markets
๐จโ๐ฌ Eligibility
โ
Science Graduate / Postgraduate
โ
6+ years of experience
โ
API manufacturing experience preferred
โ
Experience in Regulatory Affairs / DMF / Global Submissions preferred
โ Not suitable for freshers
๐ง How to Apply
๐ฉ Email: Jsoni@cohance.com
๐ Send your updated CV along with:
- Current CTC breakup ๐ฐ
- Notice Period โณ
- Relevant API Regulatory Affairs experience
๐ฐ Salary
๐ต Salary/CTC: Not specified in the vacancy.
โญ Job Highlights
๐น Senior-level Regulatory Affairs opportunity
๐น Global API regulatory submissions
๐น DMF & CEP exposure
๐น International regulated markets
๐น Ankleshwar, Gujarat
๐น 6+ years experienced candidates
๐ข Suitable for: Regulatory Affairs professionals with strong API manufacturing + DMF + global submission experience.
