Regulatory Affairs Manager
Aprazer Healthcare is seeking an experienced Regulatory Affairs Manager for their pharmaceutical facility in Haridwar. The role involves managing global regulatory dossiers, including CTD/eCTD submissions and ensuring compliance with international market standards. Candidates should have at least 10 years of relevant experience and a strong background in pharmaceutical product registration. This position requires coordinating with internal teams and external authorities to maintain regulatory compliance.
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Experience
10+ years
Function
Operations
Work mode
Onsite, India
Company
Tier 2
What you will work on
Aprazer Healthcare is seeking an experienced Regulatory Affairs Manager for their pharmaceutical facility in Haridwar. The role involves managing global regulatory dossiers, including CTD/eCTD submissions and ensuring compliance with international market standards. Candidates should have at least 10 years of relevant experience and a strong background in pharmaceutical product registration. This position requires coordinating with internal teams and external authorities to maintain regulatory compliance.
TAL's take
Stable mid-tier pharmaceutical role with clear expectations, though company status is less established.
Well-defined responsibilities and specific pharmaceutical regulatory requirements are outlined.
Must haves
- 10 years of experience in Pharmaceutical Regulatory Affairs
- B.Pharm or M.Pharm degree
- Experience with CTD/eCTD formats
- Knowledge of global regulatory requirements
- Experience with international market submissions
Tools and skills
About the company
unfamiliar company, default mid-tier