Manager/Sr. Manager-DRA Jobs in Verve Human Care Laboratories - Ahmedabad, Gujarat

Manager/Sr. Manager-DRA Jobs in Verve Human Care Laboratories - Ahmedabad, Gujarat

work outline icon10 - 15 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Verve Human Care Laboratories

time outline iconAhmedabad, Gujarat, India

Posted on 03-07-2026

1 Vacancy

Description

  • Job Title: Manager/Sr. Manager-DRA
  • Qualification: BPharm
  • Location: Verve Human Care Laboratories - Ahmedabad, Gujarat
  • Work Experience: 10 to 15 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 Verve Human Care Laboratories - Ahmedabad, Gujarat as a Manager/Sr. Manager-DRA in Ahmedabad, Gujarat 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

Verve Human Care Laboratories is a pharmaceutical company focused on developing, manufacturing, and marketing high-quality pharmaceutical formulations and healthcare products with an emphasis on innovation, regulatory compliance, and quality standards. The role involves working in a professional pharmaceutical environment to support production, quality assurance, quality control, documentation, and operational activities. Responsibilities include maintaining GMP compliance, handling manufacturing and quality records, coordinating with cross-functional teams, monitoring production and quality processes, and supporting smooth business operations. The role also requires strong analytical skills, teamwork, adherence to regulatory guidelines, and commitment to delivering safe, effective, and high-quality pharmaceutical products and healthcare solutions.

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