Jubilant Pharma Hiring Executive Regulatory Affairs
Location: Greater Noida, Uttar Pradesh
Experience: 2 – 4 Years
Qualification: B.Pharm, M.Pharm, M.Sc, B.Sc, Life Sciences
Application Deadline: February 21, 2025
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About Jubilant Pharma Limited
Jubilant Pharma Limited is a global leader in integrated pharmaceutical solutions. The company operates in two major segments: Jubilant Pharma Hiring Executive Regulatory Affairs
- Specialty Pharmaceuticals: Radiopharmaceuticals, contract manufacturing of sterile injectables, non-sterile products, and allergy therapy products.
- Generics & APIs: Solid dosage formulations and active pharmaceutical ingredients.
With advanced R&D hubs in Noida and Mysore and cutting-edge manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, Jubilant is known for its innovation and commitment to global healthcare.
Job Role: Executive – Regulatory Affairs
As an Executive – Regulatory Affairs, you will ensure compliance with global regulatory standards. You’ll manage regulatory filings, intellectual property rights, and work with cross-functional teams to bring innovative pharmaceutical products to global markets. Jubilant Pharma Hiring Executive Regulatory Affairs
Key Responsibilities
- Prepare and submit regulatory filings for APIs, solid dosage formulations, and sterile injectables.
- Collaborate with R&D teams in Noida and Mysore for product development and compliance.
- Ensure adherence to guidelines from USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA.
- Manage intellectual property rights (IPR) and contribute to patent portfolio development.
- Support audits and inspections at manufacturing facilities in Mysore and Roorkee.
Why Join Jubilant Pharma?
World-Class Facilities
- Mysore Facility: A 69-acre, USFDA-approved site specializing in APIs for global markets.
- Roorkee Facility: Multi-audited plant approved by USFDA, Japan PMDA, UK MHRA, and others for B2B dosage manufacturing across various markets. Jubilant Pharma Hiring Executive Regulatory Affairs
Strong R&D Backbone
- A dedicated team of 500+ R&D professionals.
- In-house 80-bed BA/BE facility approved by USFDA, EMEA, and ANVISA.
Career Growth Opportunities
- Rapidly growing revenue and global market presence.
- Opportunities for professional growth and leadership roles in regulatory affairs.
Who Can Apply?
Qualifications & Skills
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or Life Sciences.
- 2-4 years of experience in regulatory affairs within the pharmaceutical industry.
- Knowledge of global regulatory guidelines (USFDA, WHO, etc.).
- Strong analytical and problem-solving skills.
- Excellent communication and teamwork abilities.
Location: Noida, Mysore, or Roorkee (final location to be confirmed during the selection process).
Apply Now to join Jubilant Pharma and contribute to shaping the future of global healthcare.
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