Regulatory affairs jobs at Sun Pharma for life science professionals in Baroda
Sun Pharma Regulatory Affairs Jobs – Executive Role in R&D
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Regulatory Affairs Jobs at Sun Pharma for Life Science Graduates | Apply Now

Regulatory affairs jobs at Sun Pharmaceutical Industries Ltd offer rewarding life science jobs for professionals eager to work on global regulatory submissions and product lifecycle management. This Executive – Regulatory Affairs role strengthens Sun Pharma jobs by providing hands-on exposure to CMC documentation, regulatory approvals, and MENA market submissions within a collaborative R&D environment.

  • Job Title: Executive – Regulatory Affairs
  • Business Unit: R&D1 Regulatory Affairs
  • Job Grade: G12A
  • Location: Baroda

About the Company:

Sun Pharmaceutical Industries Ltd is one of India’s largest and most trusted pharmaceutical companies, operating across global markets. Known for innovation, quality, and patient-centric healthcare solutions, Sun Pharma jobs empower professionals to grow, lead, and thrive while contributing to life-changing medicines worldwide.

Job Overview:

This role focuses on regulatory submissions, renewals, variations, and lifecycle management for pharmaceutical products across MENA markets. Among today’s regulatory affairs jobs, this position plays a key role in ensuring timely approvals through high-quality dossier preparation and regulatory compliance.

Educational Requirements:

  • M.Sc. in Life Sciences

Key Responsibilities:

  • Prepare and review CMC dossiers for new submissions and renewals
  • Review development reports, scale-up documents, specifications, stability protocols, and artworks
  • Prepare and respond to regulatory deficiencies to enable product approvals
  • Manage lifecycle variations including API changes, site changes, and harmonization
  • Ensure regulatory compliance and maintain updated product history records
  • Coordinate approval packages and update central regulatory repositories
  • Review regulatory impact of variations and change controls

Skills Required:

  • Strong knowledge of pharmaceutical regulatory affairs and CMC documentation
  • Understanding of global regulatory submission processes
  • Attention to detail and documentation accuracy
  • Ability to collaborate with cross-functional stakeholders
  • Clear written and verbal communication skills

For professionals seeking long-term growth in regulatory affairs jobs, this opportunity at Sun Pharma offers global exposure, structured learning, and career progression. Among competitive life science jobs, Sun Pharma jobs stand out for their innovation-driven culture and commitment to professional development.

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