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Moribus Pharma Walk-in Interview 2026 – Regulatory Affairs Specialist (FDF) Jobs in Surat

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Moribus Pharma is hiring Regulatory Affairs Specialist for FDF (Finished Dosage Formulation) through a walk-in interview from 8th to 12th June 2026 in Surat. This is a great pharma jobs opportunity for B.Pharm professionals with 1+ year experience in regulatory affairs and Module 3 dossier compilation.

About the Company

Moribus Pharma is a growing pharmaceutical company specializing in Finished Dosage Formulations (FDF). Committed to quality, innovation, and regulatory excellence, the company focuses on developing and manufacturing high-standard pharmaceutical products.

With a strong emphasis on compliance and continuous improvement, Moribus Pharma is expanding its presence in the competitive Indian pharma industry while maintaining global quality standards.

Job Details

  • Company Name: Moribus Pharma
  • Experience: 1+ Years
  • Qualification: B.Pharm
  • Location: Surat, Gujarat
  • Work Type: On-site

Job Description

Moribus Pharma is actively recruiting a Regulatory Affairs Specialist for its FDF division. The role is critical for Module 3 dossier preparation, compilation, and regulatory submissions. This walk-in drive offers a strong platform for experienced professionals seeking pharmaceutical careers in India in the regulatory domain.

Regulatory Affairs Specialist – FDF

  • Department: Regulatory Affairs
  • Role: Regulatory Affairs Specialist
  • Experience: 1+ Years
  • Education/Qualification: B.Pharm

Skills/Qualifications

  • Minimum 1 year experience in Regulatory Affairs in Pharmaceutical Industry
  • Strong understanding of Module 3 preparation and compilation
  • Knowledge of dossier compilation for Finished Dosage Formulations
  • Familiarity with regulatory submissions and compliance requirements
  • Excellent documentation and analytical skills
  • Surat local candidates preferred

Key Responsibilities

  • Prepare and compile Module 3 dossiers for FDF
  • Support regulatory submissions and approvals
  • Ensure compliance with regulatory guidelines
  • Review and update technical documentation
  • Coordinate with internal teams for dossier requirements
  • Maintain regulatory records and audit readiness

Benefits/Perks

  • Career growth in Regulatory Affairs
  • Opportunities to work on FDF projects
  • Learning and development in regulatory domain
  • Collaborative and growth-oriented work culture
  • Competitive compensation package

How to Apply

Moribus Pharma is hiring Regulatory Affairs Specialist for FDF (Finished Dosage Formulation) through a walk-in interview from 8th to 12th June 2026 in Surat.

Interested and eligible candidates should attend the walk-in interview directly at the venue with updated resume and relevant documents.

For more pharma jobs and walk-in interviews across India, visit Pharma Recruiter.

Don’t miss this opportunity — attend the walk-in and advance your regulatory career!

Walk-in Interview Details

  • Date: 8th June to 12th June 2026
  • Time: 11:00 AM to 6:00 PM
  • Venue: Prime Shoppers, Moribus Pharma, 4th Floor (425), Vesu, Rundh, Surat-395007, Gujarat
  • Contact: Not specified (walk-in only)

Note: Local candidates from Surat are preferred.

Why You Should Join

Moribus Pharma offers a dynamic and supportive environment focused on innovation, regulatory compliance, and employee growth. Joining the company provides long-term career stability, recognition for your regulatory expertise, and opportunities to contribute to high-quality FDF development. With a strong emphasis on learning and professional development, it is an ideal place to build a successful career in the pharmaceutical regulatory field.

FAQs

Q1: What is the minimum experience required?

A: At least 1 year of experience in Regulatory Affairs in the Pharmaceutical Industry.

Q2: What qualification is needed?

A: B.Pharm degree is required.

Q3: Is this a walk-in interview?

A: Yes, walk-in interviews will be held from 8th to 12th June 2026.

Q4: Are local candidates preferred?

A: Yes, candidates local to Surat are preferred.

Q5: What is the focus area of the role?

A: Module 3 preparation, compilation, and regulatory submissions for FDF.

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