Brawn Laboratories Recruitment 2026: DRA Officer (LATAM Market) Vacancy for B.Pharm & M.Pharm Graduates

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Are you looking to build a rewarding career in Drug Regulatory Affairs (DRA)? If you have experience in LATAM dossier preparation and want to work with an internationally recognized pharmaceutical company, then this opportunity could be the next step in your professional journey.

Brawn Laboratories Limited is inviting applications for the position of DRA Officer (LATAM Market) at its Faridabad, Haryana facility. This role is ideal for B.Pharm and M.Pharm graduates with 1–2 years of regulatory affairs experience, especially those familiar with CTD/eCTD dossier preparation and international pharmaceutical regulations.

If you’re eager to gain global regulatory exposure and work on international product registrations, read this detailed job guide to learn everything about the vacancy, eligibility, responsibilities, and application process.

📌 Job Overview

ParticularDetails
CompanyBrawn Laboratories Limited
PositionDRA Officer (LATAM Market)
DepartmentDrug Regulatory Affairs
Experience1–2 Years
QualificationB.Pharm / M.Pharm
LocationFaridabad, Haryana
Employment TypeFull-Time
Application ModeEmail

🏢 About Brawn Laboratories Limited

Brawn Laboratories Limited is a reputed Indian pharmaceutical company engaged in the manufacturing and marketing of quality pharmaceutical formulations. The company has built a strong presence in domestic and international markets through its WHO-GMP compliant manufacturing facilities and commitment to quality.

With exports across several countries, Brawn Laboratories offers professionals an opportunity to work in global regulatory environments and gain exposure to international pharmaceutical standards.

💼 About the DRA Officer (LATAM Market) Role

Drug Regulatory Affairs professionals ensure pharmaceutical products comply with the legal and scientific requirements of different countries before they reach patients.

In this role, you’ll primarily manage product registrations and regulatory documentation for the Latin American (LATAM) market, making it an excellent opportunity for professionals interested in international regulatory affairs.

🎯 Key Responsibilities

Selected candidates will be responsible for:

✅ Preparing registration dossiers for LATAM countries.

✅ Compiling CTD and eCTD documents.

✅ Managing product lifecycle activities including:

  • Variations
  • Renewals
  • Amendments
  • Product maintenance

✅ Coordinating with:

  • Quality Assurance
  • Quality Control
  • Research & Development
  • Manufacturing
  • Documentation teams

✅ Preparing responses to regulatory authority queries.

✅ Monitoring changing regulatory guidelines in Latin American countries.

✅ Ensuring all submissions meet country-specific compliance requirements.

🎓 Educational Qualification

Applicants should possess:

  • Bachelor of Pharmacy (B.Pharm)
    OR
  • Master of Pharmacy (M.Pharm)

from a recognized university.

⏳ Experience Required

Candidates should have:

  • 1–2 years of Regulatory Affairs experience.

Preference will be given to candidates having practical exposure in:

  • LATAM dossier preparation
  • International pharmaceutical registrations
  • Regulatory documentation

💡 Required Skills

The ideal candidate should have knowledge of:

  • CTD documentation
  • eCTD submissions
  • Drug registration procedures
  • Pharmaceutical regulations
  • Documentation management
  • Regulatory compliance
  • Technical writing
  • Communication skills
  • Time management
  • Attention to detail

🌍 Why Choose a Career in LATAM Regulatory Affairs?

Regulatory Affairs professionals handling international markets are among the most sought-after professionals in the pharmaceutical industry.

Some major benefits include:

🌎 International Exposure

You’ll gain experience dealing with health authorities from multiple countries.

📈 Excellent Career Growth

Regulatory professionals often move into senior positions such as:

  • Senior DRA Executive
  • Regulatory Affairs Manager
  • Global Regulatory Lead
  • International Compliance Specialist

💼 High Industry Demand

Companies exporting pharmaceutical products continuously require skilled regulatory professionals.

📚 Continuous Learning

Every country has unique regulations, making this career intellectually rewarding.

🚀 Why Work at Brawn Laboratories?

Working at Brawn Laboratories offers several advantages:

✔ International exposure

✔ Professional learning

✔ Stable pharmaceutical organization

✔ Opportunity to work on global product registrations

✔ Collaborative work culture

✔ Strong career development prospects

📧 How to Apply?

Interested candidates can apply by sending their updated resume via email.

Email Your Resume To:

📩 talentacq@brawnlabs.in

Recruitment Contact

📞 +91-8130266355

📝 Email Subject Example

Use a professional subject line such as:

Application for DRA Officer (LATAM Market) – Your Name

Include the following details in your email:

  • Current Company
  • Total Experience
  • Relevant LATAM Experience
  • Current CTC
  • Expected CTC
  • Notice Period
  • Contact Number

📄 Documents to Keep Ready

Before applying, prepare:

  • Updated Resume
  • Educational Certificates
  • Experience Letters
  • Latest Salary Slip (if applicable)
  • Regulatory Experience Details

🌟 Tips to Increase Your Selection Chances

  • Highlight your LATAM dossier experience clearly.
  • Mention CTD/eCTD expertise prominently.
  • Include software or regulatory tools you’ve worked with.
  • Showcase successful product registrations or submissions.
  • Proofread your resume before sending it.

📈 Career Scope After Regulatory Affairs

Professionals in Drug Regulatory Affairs can explore opportunities in:

  • Pharmaceutical Manufacturing
  • CROs
  • Global Regulatory Consulting
  • Biotech Companies
  • Medical Device Companies
  • International Pharmaceutical Firms

With experience, professionals may also work in regulated markets like:

  • USFDA
  • EMA
  • MHRA
  • GCC
  • ASEAN
  • LATAM

❓ Frequently Asked Questions (FAQs)

1. Who can apply?

Candidates with B.Pharm or M.Pharm qualifications and 1–2 years of Regulatory Affairs experience.

2. Are freshers eligible?

The company prefers experienced candidates. However, candidates with strong internship or industrial training in Regulatory Affairs may still consider applying.

3. Where is the job located?

Faridabad, Haryana.

4. What market will I handle?

The role focuses on the LATAM (Latin America) pharmaceutical market.

5. What documents should I include?

Resume, educational details, experience information, current CTC, expected CTC, and notice period.

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