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Nevisun Pharmaceuticals Hiring For Regulatory Affairs

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Nevisun Pharmaceuticals Pvt. Ltd

Bachelor's or Master's degree in Pharmacy or a relevant Life Sciences

Surat, Gujarat

2–4 Years

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Nevisun Pharmaceuticals Pvt. Ltd. has announced an excellent career opportunity for experienced Regulatory Affairs Executives to join its formulation pharmaceutical team in Surat, Gujarat. The company is looking for female candidates with 2 to 4 years of experience in pharmaceutical regulatory affairs, particularly in African market dossier compilation and regulatory submissions.

If you have expertise in handling regulatory documentation, post-submission queries, and African pharmaceutical registration processes, this is a great opportunity to advance your career with a growing pharmaceutical organization.

Job Highlights

  • Company: Nevisun Pharmaceuticals Pvt. Ltd.
  • Position: Regulatory Affairs Executive
  • Department: Regulatory Affairs
  • Location: Surat, Gujarat
  • Industry: Pharmaceutical (Formulation / Finished Dosage Form)
  • Experience: 2–4 Years
  • Eligibility: Female Candidates Only (as specified by the employer)
  • Local Candidates Preferred: Surat

Key Responsibilities

As a Regulatory Affairs Executive, you will be responsible for:

  • Preparing and compiling regulatory dossiers for African countries.
  • Managing pharmaceutical product registration documentation.
  • Handling regulatory authority queries after dossier submission.
  • Coordinating with internal departments for required documentation.
  • Ensuring compliance with country-specific regulatory guidelines.
  • Maintaining accurate regulatory records and documentation.
  • Supporting product registrations and lifecycle management activities.
  • Keeping updated with changing African pharmaceutical regulations.

Required Qualifications

Candidates should possess:

  • Bachelor’s or Master’s degree in Pharmacy or a relevant Life Sciences discipline.
  • 2–4 years of Regulatory Affairs experience in Formulation/FDF pharmaceutical companies.
  • Hands-on experience in African Market dossier preparation.
  • Strong knowledge of CTD/eCTD documentation.
  • Excellent documentation and communication skills.
  • Good understanding of pharmaceutical regulatory compliance.

Preferred Skills

  • African market registration expertise.
  • Regulatory query response management.
  • Dossier compilation.
  • Documentation review.
  • Regulatory compliance.
  • Pharmaceutical product registration.
  • Attention to detail.
  • Team collaboration.

Salary

Based on industry standards for Surat pharmaceutical companies, the expected salary is:

₹4.8 LPA – ₹7.2 LPA (Approx.)

Actual compensation will depend upon experience, technical expertise, and interview performance.

Why Join Nevisun Pharmaceuticals?

  • Growing pharmaceutical organization.
  • Exposure to international regulatory markets.
  • Opportunity to work on African pharmaceutical registrations.
  • Professional growth in Regulatory Affairs.
  • Collaborative work environment.
  • Career advancement opportunities.

How to Apply

Interested female candidates can apply through:

Email: hr@nevisunpharma.com

Nevisun Pharmaceuticals Hiring For Regulatory Affairs
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