This position offers a chance to work in a dynamic environment focused on generic pharmaceuticals for emerging markets. As an individual contributor, you’ll apply your regulatory knowledge to help maintain licenses, prepare submissions, and drive process improvements.
Roles & Responsibilities
- Plan, prepare, and execute simple regulatory submissions while assisting with more complex dispatches and planning.
- Ensure timely compliance for new product registrations and renewals of existing products.
- Apply sound judgment in interpreting and following policies, regulations, and guidelines.
- Understand and implement relevant regulatory standards, promotional guidelines, and government regulations.
- Perform gap analysis on registration dossiers to confirm full compliance before submission.
- Proactively communicate important issues, key topics, and updates to managers and cross-functional teams.
- Collaborate effectively with other departments to resolve regulatory challenges.
Required Qualifications
- Education: B.Pharm or M.Pharm (essential).
- Preferred: Additional specialization in Formulation & Development or Pharmaceutical Technologies.
- Experience: 1-3 years in Regulatory Affairs, specifically with Solid Oral Dosage Forms. Relevant experience in Quality Control or R&D will be considered a strong advantage.
- Strong knowledge of regulatory requirements for pharmaceutical products in India.
- Good communication, problem-solving, and teamwork skills.
- Ability to work independently while contributing to team goals.
Salary, Benefits & How to Apply
Pelltech Healthcare offers a competitive compensation package suitable for this junior-level role in the Mumbai pharmaceutical sector. The expected salary range is ₹3.5 – 6.0 LPA (Lakhs Per Annum), depending on experience, qualifications, and negotiation.
Benefits typically include:
- Health insurance
- Performance-based incentives
- Professional development opportunities
- Supportive work environment in a growing pharma company
To apply, visit the official Pelltech Healthcare website or LinkedIn company page to submit your resume and cover letter. Reference the position “Junior Executive – Regulatory Affairs” in your application. Direct applications through company channels are recommended for fastest consideration.
