Asst. Manager/Dy. Manager-DRA Jobs in Ravian Life Science Pvt Ltd - Haridwar, Uttarakhand

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Asst. Manager/Dy. Manager-DRA Jobs in Ravian Life Science Pvt Ltd - Haridwar, Uttarakhand

work outline icon10 - 12 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Ravian Life Science Pvt Ltd

time outline iconHaridwar, Uttarakhand, India

Posted on 16-07-2026

1 Vacancy

Description

  • Job Title: Asst. Manager/Dy. Manager-DRA
  • Qualification: BPharm (Bachelor Of Pharmacy)
  • Location: Ravian Life Science Pvt Ltd - Haridwar, Uttarakhand
  • Work Experience: 10 to 12 Years

Job Description

  • Prepare, review, and submit regulatory documents to local and international health authorities.
  • Ensure compliance with national and international regulatory guidelines (FDA, EMA, CDSCO, etc.).
  • Maintain up-to-date knowledge of regulatory requirements for pharmaceuticals, devices, or biotech products.
  • Coordinate with R&D, QA, and Production teams to gather required data for submissions.
  • Track submission timelines and ensure timely approvals for product registrations.
  • Review and approve product labeling, packaging, and promotional materials from a regulatory perspective.
  • Respond to regulatory queries and inspections from authorities.
Take this opportunity to join Ravian Life Science Pvt Ltd - Haridwar, Uttarakhand as a Asst. Manager/Dy. Manager-DRA in Haridwar, Uttarakhand and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Regulatory Affairs / Pharmacovigilance

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

Attention to DetailProblem Solving SkillsAnalytical SkillsDocumentation

About Organization

Ravian Life Science Pvt Ltd is a pharmaceutical and life sciences company focused on developing, manufacturing, and supplying high-quality pharmaceutical formulations and healthcare products. The role involves supporting production, quality assurance, quality control, and documentation activities. Responsibilities include maintaining GMP compliance, monitoring manufacturing processes, and coordinating with cross-functional teams. The role requires strong analytical skills, teamwork, and adherence to regulatory guidelines. It also demands a commitment to delivering safe, effective, and high-quality pharmaceutical products.

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