Sun Pharma is Hiring for Executive Job Role | M Pharm Graduates Join By Applying Now

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MPharma Job Vacancies at Sun Pharma
Sun Pharma Hiring for Executive Job Role | M Pharm Graduates Apply Now

MPharma Job Vacancies at Sun Pharma

Sun Pharmaceutical Industries Ltd, India’s leading pharmaceutical company, is hiring for the position of Executive – FRD Non-Orals at its R&D center in Baroda. This role offers an excellent opportunity for M.Pharm graduates with 1–3 years of experience to contribute to the development of innovative non-oral dosage forms, regulatory submissions, and technology transfer activities. Join Sun Pharma and be part of a team dedicated to advancing healthcare through continuous innovation.

  • Job Position: Executive – FRD Non Orals
  • Business Unit: R&D1 Regulatory Affairs
  • Job Grade: G12A
  • Location: Baroda (Tandalja – R&D Center)

About the Company

Sun Pharmaceutical Industries Ltd is the fourth-largest specialty generic pharmaceutical company in the world and India’s No. 1 pharma brand. Headquartered in Mumbai, Sun Pharma provides high-quality, affordable medicines trusted by healthcare professionals and patients in over 100 countries. With a strong emphasis on innovation, research, and patient care, Sun Pharma empowers its employees to grow while contributing to global healthcare solutions.

Education:

MPharm

Experience:

1-3 years in formulation development or regulatory projects

Skills Required:

  • Strong knowledge of QbD principles and non-oral dosage form development
  • Proficiency with MINITAB and eLNB/METIS software
  • Good understanding of regulatory requirements for ANDA submissions
  • Strong communication, documentation, and problem-solving abilities

Key Responsibilities

  • Design and conduct experiments for preformulation and formulation optimization of complex non-oral dosage forms.
  • Execute experiments as per the Design of Experiments (DoE).
  • Conduct literature searches and prepare summary reports for ANDA projects.
  • Prepare product development study protocols, reports, and regulatory submission documents.
  • Record experimental details in eLNB/METIS software and analyze results using MINITAB.
  • Draft Technology Transfer documents, risk assessments, and regulatory justifications.
  • Prepare stability protocols and product development reports in accordance with global requirements.
  • Support pre-ANDA meeting packages, scientific justifications, and regulatory submissions.
  • Draft SOPs and participate in equipment qualification activities.
  • Coordinate with ADD, RA, CQA, and plant teams for project execution.
  • Ensure compliance with internal quality systems during all activities.

Employee Benefits at Sun Pharma

At Sun Pharma, employee success and well-being are top priorities. The company offers comprehensive benefits, professional growth opportunities, and a collaborative work environment that empowers individuals to innovate and make a global impact.

APPLY ONLINE HERE

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