Hetero Labs Careers Regulatory Affairs Professionals Wanted

Hetero Labs Hiring for Regulatory Affairs Professionals

Hetero Labs Limited, a leading global pharmaceutical company committed to providing affordable and high-quality healthcare solutions. With a focus on innovation, research, and development, Hetero Labs has established itself as a key player in the pharmaceutical industry. We take pride in our diverse team, cutting-edge technology, and a relentless pursuit of excellence.

Hetero Vacancies List

Position Title: Regulatory Affairs Professional

• Company Name: Hetero Labs Limited
• Location: Sai Rd, near Homeland City, Baddi, Himachal Pradesh 173205
• Qualification: B.Pharm. / M.Pharm.
• Experience: 1 to 3 years

Job Description

About the Department & Responsibilities

Joining our Regulatory Affairs team at Hetero Labs means contributing to a crucial aspect of pharmaceutical operations. Key responsibilities include:

1. Local FDA Application:
   • Submission and management of local FDA applications like COPP, FSC, product permission, MMC, test license.
2. Quality Document Review:
   • Thorough review of quality documents for dossier preparation.
3. Export ROW Dossier Preparation:
   • Preparation of regulatory dossiers for export to regions like Africa, ASEAN, LATAM, etc.
4. Coordination and Communication:
   • Collaborate with other departments for RA-related work and ensure effective coordination.
5. RA Data Management:
   • Efficiently manage regulatory affairs data to meet compliance and reporting requirements.

Additional Details

• Role: Regulatory Affairs Professional
• Industry Type: Pharmaceutical
• Department: Regulatory Affairs
• Employment Type: Full-Time
• Role Category: Pharmaceutical Operations
• Education:
  • UG: B.Pharm.
  • PG: M.Pharm.

How to Apply

If you are a qualified and motivated Regulatory Affairs Professional, we invite you to be part of our dynamic team. Please send your resume to anil.j@hetero.com or srinivasarao.da@hetero.com.

Key Skills

Regulatory Affairs, FDA Applications, Dossier Preparation, Quality Document Review, Export Regulations, Communication, Data Management