Are you passionate about pharmaceutical regulations and ready to contribute to international markets? If yes, Sovvaka Global is urgently hiring for the role of Regulatory Affairs (RA) Officer for ROW (Rest of World) markets at their Mumbai – Andheri East location.
This opportunity is ideal for professionals with 1-2 years of regulatory affairs experience who want to work in a fast-paced, compliance-driven environment and gain global exposure.
🏢 About Sovvaka Global
Sovvaka Global is an emerging name in the pharmaceutical sector, known for its expertise in regulatory compliance and dossier submissions across various international markets including LATAM, EU, Asia, and Africa. The company is building a reputation for delivering accurate, timely, and strategic regulatory solutions.
Sovvaka offers a platform where you can grow professionally, sharpen your regulatory knowledge, and collaborate with cross-functional teams to ensure global quality standards.
👨⚕️ Role: Regulatory Affairs Officer / Executive
📍 Location: Mumbai (Andheri East)
🕒 Experience: 1 – 2 Years
🎓 Qualification: B.Pharm / M.Pharm / M.Sc / PGD-RA
💼 Employment Type: Full-time
💸 Salary Range: ₹3.5 – 5.5 LPA (Based on interview & experience)
📋 Job Description
The Regulatory Affairs Officer will work on compiling, reviewing, and coordinating regulatory submissions for ROW markets. This includes ensuring that dossiers are compliant with international guidelines, coordinating with internal teams, and handling queries from health authorities efficiently.
This position is perfect for candidates who are detail-oriented, understand regulatory frameworks, and have a passion for cross-border compliance management.
✅ Key Responsibilities
Your day-to-day responsibilities as an RA Officer will include:
✔ Reviewing and compiling regulatory dossiers for submission in Rest of World (ROW) markets.
✔ Addressing and responding to regulatory queries from health authorities in regions like LATAM, Asia, and Africa.
✔ Ensuring complete compliance with local and international regulations.
✔ Coordinating with internal departments (QA, QC, Production, and Packaging) for necessary documents and updates.
✔ Checking artworks for labeling compliance and correcting any regulatory discrepancies.
✔ Maintaining an updated knowledge base of regulatory norms and changes globally.
🔍 Skills Required
To excel in this role, you should have the following:
- 1–2 years of hands-on regulatory affairs experience in the pharma industry.
- Working knowledge of ROW market regulations (especially LATAM, EU, Africa, and Asia).
- A keen eye for detail, especially in dossier preparation and data verification.
- Basic understanding of artwork review and packaging regulations.
- Good written and oral communication skills to handle both internal and external interactions.
- Effective time management and the ability to meet submission deadlines.
💡 Preferred but Not Mandatory:
🔹 Experience with CTD/eCTD submissions.
🔹 Familiarity with regulatory software, databases, and documentation systems.
🔹 Exposure to multiple regulatory jurisdictions and country-specific formats.
Even if you don’t have these, you’re still eligible—Sovvaka is open to training high-potential candidates who show promise.
🏙️ Why Work at Sovvaka Global?
Joining Sovvaka Global means becoming part of a growth-focused team in the regulatory affairs space. Here’s what makes this job special:
🌐 Global Market Exposure: You’ll get hands-on experience with ROW submissions, giving your career a global edge.
🧠 Skill Enhancement: Sovvaka supports continual learning with opportunities for cross-training and document automation tools.
👨👩👧👦 Team Culture: Friendly and collaborative team dynamics, with mentorship for early-career professionals.
📈 Career Growth: With the pharma sector booming, especially in regulatory roles, you’re positioned for fast-tracked growth.
💸 Salary Expectations
If you have 1–2 years of experience in regulatory affairs and are based in Mumbai or willing to relocate, you can expect a CTC of ₹3.5 – 5.5 LPA, based on your technical skills, market knowledge, and interview performance.
For candidates with more advanced experience in ROW regulatory environments, negotiable packages are possible.
📩 How to Apply
Sovvaka is inviting email applications for this role. Here’s how to apply professionally:
- Step 1: Update your CV with your latest experience and regulatory projects.
- Step 2: Compose an email and attach your CV.
- Step 3: Use the subject line:
📌 “Application for RA Officer – Mumbai – [Your Full Name]” - Step 4: Email it to: hr@sovvakaglobal.com
🧩 Final Thoughts
This urgent hiring by Sovvaka Global is a golden opportunity for those looking to build a solid career in Regulatory Affairs for international markets. With hands-on dossier preparation, real-time authority interaction, and multi-market exposure, this role offers more than a paycheck—it offers progress.
If you’re ready to contribute to global health compliance and accelerate your pharma career, this job is tailor-made for you.
Don’t delay—send your CV today and take your regulatory career global with Sovvaka!
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