Cadila Pharmaceuticals Hiring for Regulatory Affairs (API) Officer to Sr. Executive
Cadila Pharmaceuticals Recruitment drive for Regulatory Affairs (API) Officer to Sr. Executive
Cadila Pharmaceuticals, one of India’s leading pharmaceutical companies, is currently seeking talented individuals to join their Regulatory Affairs (API) team. This exciting opportunity is open for positions ranging from Officer to Sr. Executive at their Dholka Plant in Gujarat. If you have an M.Sc or M.Pharm degree and experience in eCTD compilation of Drug Master Files and CEP submissions, this could be the perfect career move for you!
About Cadila Pharmaceuticals
Cadila Pharmaceuticals is renowned for its innovation and excellence in the pharmaceutical industry. With a robust portfolio of products and a commitment to improving global health, Cadila offers a dynamic and rewarding work environment. Joining Cadila means becoming a part of a team that values expertise, growth, and the pursuit of excellence.
Job Details
Department: Regulatory Affairs (API)
Position: Officer to Sr. Executive
Location: Cadila Pharmaceuticals Ltd, Survey No 1389, Trasad Road, Dholka, Gujarat 382225
Experience: 1 to 4 Years
Qualification: M.Sc / M.Pharm
Key Responsibilities:
- eCTD Compilation: Prepare and compile electronic Common Technical Document (eCTD) submissions for Drug Master Files and CEPs.
- Regulatory Submissions: Handle submission portals for regulatory filings.
- Documentation: Maintain accurate records and documentation to support regulatory submissions.
- Compliance: Ensure all activities comply with regulatory guidelines and company policies.
How to Apply
Interested candidates who meet the qualifications are invited to attend the walk-in interview:
Date: 05-07-2024, Friday
Time: 9:00 am to 3:00 pm
Venue: Cadila Pharmaceuticals Ltd, Survey No 1389, Trasad Road, Dholka, Gujarat 382225
For those unable to attend the interview, please send your CV to sharad.yadav@cadilapharma.com or shailendra.r@cadilapharma.com.
Qualifications and Experience
To qualify for this role, candidates must have:
- Educational Background: M.Sc / M.Pharm degree.
- Experience: 1 to 4 years of experience in regulatory affairs, specifically in eCTD compilation and CEP submissions.
- Skills: Proficiency in using submission portals and maintaining regulatory documentation.
Walk-In Interview Details
Candidates who fulfill the above requirements are encouraged to participate in the walk-in interview. Please bring your bio-data, original certificates, and copies of certificates to prove your age, qualification, and experience.
