Regulatory Affairs Jobs 2026: Junior & Mid-Level Executive Openings for B.Pharm

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👉 ENROL IN THE PHARMACEUTICAL REGULATORY AFFAIRS COURSE ON UDEMY

Looking for Regulatory Affairs jobs for B.Pharm graduates in 2026? Two openings are available for Junior Regulatory Affairs Executive and Mid-Level Regulatory Affairs Executive positions in the Regulatory Affairs – ROW (Rest of the World) Markets department.

These opportunities are relevant to pharmacy graduates and regulatory affairs professionals interested in international pharmaceutical product registrations, CTD dossier preparation, regulatory submissions, and compliance documentation.

According to the available recruitment details, the salary ranges from ₹3 LPA to ₹8 LPA, depending on the position. Interested candidates can send their updated resumes to the recruitment contact listed below.

Regulatory Affairs Recruitment 2026 – Job Overview

  • Job Department: Regulatory Affairs – ROW Markets
  • Industry: Pharmaceutical
  • Job Positions: Junior Regulatory Affairs Executive, Mid-Level Regulatory Affairs Executive
  • Total Vacancies: 2
  • Qualification: B.Pharm
  • Salary: ₹3–4 LPA for Junior; ₹7–8 LPA for Mid-Level
  • Application Mode: Email
  • HR Contact: Shaikh Altaf
  • Email: see in how to apply
  • Phone: 8446710878
  • Job Location: Not specified
  • Experience Required: Not specified; confirm with HR

Note: The employer name, job location, experience requirements, and current vacancy status have not been independently confirmed. Candidates should verify these details with the recruiter before applying.

1. Junior Regulatory Affairs Executive

Vacancies: 1
Salary: ₹3–4 LPA
Qualification: B.Pharm

The Junior Regulatory Affairs Executive position may suit candidates looking to develop their careers in pharmaceutical regulatory affairs and international product registration.

Key Responsibilities

  • Assist with pharmaceutical product registrations in ROW markets.
  • Support the preparation and compilation of Common Technical Document (CTD) dossiers.
  • Help prepare regulatory submissions and documentation for product variations.
  • Track submission schedules, approval status, and regulatory deadlines.
  • Coordinate product sample submissions with relevant departments.
  • Review Certificates of Analysis (COAs), product artwork, and package leaflets.
  • Assist with product permissions and Certificate of Pharmaceutical Product (COPP) documentation.
  • Support WHO-GMP-related documentation and coordination.
  • Assist in preparing and updating Standard Operating Procedures (SOPs).
  • Maintain regulatory records and provide documentation during audits.

Candidates should have good documentation skills, attention to detail, and an interest in pharmaceutical regulations.

2. Mid-Level Regulatory Affairs Executive

Vacancies: 1
Salary: ₹7–8 LPA
Qualification: B.Pharm; additional criteria to be confirmed

This position may be suitable for regulatory affairs professionals with relevant experience in international pharmaceutical registrations, dossier preparation, and regulatory compliance.

Key Responsibilities

  • Coordinate product registrations and regulatory submissions for assigned ROW markets.
  • Prepare, compile, and review CTD dossiers.
  • Manage documentation for regulatory variations and post-approval changes.
  • Monitor submission progress, approval timelines, and regulatory queries.
  • Coordinate product sample submissions and supporting documentation.
  • Review COAs, product artwork, and package leaflets for consistency.
  • Coordinate product permissions and COPP-related requirements.
  • Support documentation associated with WHO-GMP requirements.
  • Maintain regulatory records and contribute to SOP updates.
  • Provide documentation and coordination support during manufacturing audits.

The recruiter should confirm the minimum experience requirement and specific international markets covered by this position.

Educational Qualification

The stated qualification for these Regulatory Affairs openings is Bachelor of Pharmacy (B.Pharm).

Pharmacy graduates interested in international product registration may explore the junior position, while candidates with relevant regulatory affairs experience may consider the mid-level opening.

The employer has not provided detailed eligibility criteria, so candidates should confirm the required experience, additional qualifications, and technical skills before applying.

What Is Regulatory Affairs – ROW Markets?

Regulatory Affairs is a key pharmaceutical function responsible for helping companies meet the regulatory requirements applicable to their medicinal products.

ROW stands for Rest of the World. Depending on the organization, it generally refers to international markets outside its primary or specifically designated markets.

Regulatory affairs professionals may work on:

  • Pharmaceutical product registration and renewals.
  • CTD dossier preparation and submission.
  • Regulatory variations and post-approval changes.
  • Product labeling, artwork, and package leaflet reviews.
  • Regulatory compliance and documentation.
  • Coordination with quality assurance, manufacturing, and other teams.

This field can provide opportunities to develop expertise in pharmaceutical documentation, international regulations, and product lifecycle management.

Important Regulatory Affairs Terms

1. CTD – Common Technical Document: A standardized format for organizing pharmaceutical registration information.

2. COA – Certificate of Analysis: A document containing analytical test results for a material or product.

3. COPP – Certificate of Pharmaceutical Product: A certificate used in international pharmaceutical trade and registration processes.

4. WHO-GMP: Good Manufacturing Practices associated with World Health Organization guidance.

5. Regulatory Variations: Regulatory applications or notifications for changes to an already registered pharmaceutical product.

6. SOP – Standard Operating Procedure: A controlled document describing how a process or activity should be performed.

Understanding these terms may help candidates prepare for regulatory affairs interviews.

How to Apply for Regulatory Affairs Jobs

Interested candidates can contact the recruiter using the details below.

Application Process

  1. Prepare an updated resume highlighting your B.Pharm qualification and relevant regulatory affairs skills.
  2. Mention whether you are applying for the Junior or Mid-Level Regulatory Affairs Executive position.
  3. Highlight relevant experience in CTD dossiers, product registrations, regulatory variations, COA reviews, or compliance documentation, where applicable.
  4. Include your current location, notice period, and contact information.
  5. Send your resume to altaf.shaikh@approachus.in.

Suggested Email Subject: Application for Regulatory Affairs Executive – ROW Markets

Before sharing personal documents, confirm the employer’s identity, job location, eligibility criteria, and vacancy status with the recruiter.

Conclusion

These two Regulatory Affairs Executive openings may interest B.Pharm graduates and experienced pharmaceutical professionals seeking opportunities in international product registration and regulatory compliance.

The advertised salary ranges are ₹3–4 LPA for the Junior Executive role and ₹7–8 LPA for the Mid-Level Executive role. Since several recruitment details remain unspecified, contact the recruiter to confirm eligibility and application requirements.

Share this opportunity with pharmacy graduates and regulatory affairs professionals looking for pharmaceutical jobs in 2026.

Disclaimer: This article is based on the recruitment information provided. JobsOnTheWay.com has not independently verified the employer, salary, recruiter, or vacancy status. Applicants should verify all details before proceeding.

👉 ENROL IN THE PHARMACEUTICAL REGULATORY AFFAIRS COURSE ON UDEMY