About Zydus Life Sciences:
Zydus Cadila is headquartered in Ahmedabad, India, and ranks 4th in the Indian pharmaceutical industry. The group has manufacturing sites and research facilities spread across five states Gujarat, Maharashtra, Goa, Himachal Pradesh, and Sikkim in India and the US, and Brazil.
Zydus’ global business has a strong presence in the regulated markets of the US, Europe (France and Spain), and in the high-profile markets of Latin America and South Africa. It is also present in a big way in 25 other emerging markets worldwide.
As one of the key players amongst the pharmaceutical manufacturing companies, the group has manufacturing capabilities across the entire pharmaceutical value chain: including formulations, APIs, vaccines, biosimilars, complex products (transdermals, topical, etc.), animal health products, and wellness products. It has more than 30 manufacturing plants worldwide including India, Brazil, and the USA.
In this pandemic situation, Healthcare companies have developed greater responsibilities to constantly contribute to the nation despite all odds. The employees of the pharma companies are viewed as constant warriors who are working for a larger cause of humanity by delivering essential drugs on time in India and across the world. Moreover, we are also creating job opportunities for people who want to be part of the workforce and also with the purpose to serve their well-being.
Zydus’ Innovation program is spearheaded by 1400 researchers across 19 sites, working on differentiated medicines for the future.
From NCEs to vaccines, biosimilars, and niche technologies, the group is exploring
different ideas and concepts, innovating constantly.
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About Zydus Life sciences Jobs:
INVITING CANDIDATES FOR ZYDUS LIFESCIENCES LIMITED
We are hiring for Zydus Research Centre, Ahmedabad
Biotech – Regulatory Affairs
Associate Manager / Manager / Sr. Manager
- Prepare and submit regulatory dossiers (CTD / ACTD / eCTD) / briefing package for global, emerging and domestic markets
- Manage master dossier updates and handle query responses for assigned products
- Coordinated with cross-functional teams and regulatory agencies for product registrations
- Supported post-approval changes to ensure smooth commercialization
- Assist in global filings, document reviews, gap analysis, and artwork management
- Monitor regulatory updates, perform impact analysis and ensure compliance
- Coordinate with manufacturing sites and maintain relationships with regulatory authorities.
Job Details
- Job location: Ahmedabad
- Qualification: M.Sc / B.Tech / B.Pharm / M.Pharm / M.Tech / Ph.D in Biotechnology, Micro.
- Experience: 8 years and above in Regulatory Affairs
