Job Description

Job Description

Regulatory Knowledge & Compliance

  • Demonstrate strong understanding of the Drugs and Cosmetics Act, Central Drugs Standard Control Organization, Guidance for Industry, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Regulations, and Narcotic Drugs and Psychotropic Substances Act.
  • Ensure compliance with all applicable regulatory requirements for pharmaceutical products.

CDSCO Regulatory Submissions

  • Strategize, prepare, submit, and obtain approvals for:
    • FORM 11, CT-17, CT-04, CT-21, CT-18
    • Form 10
    • MD-5, MD-6, MD-15, MD-17
    • Dual NOC applications
  • Ensure timely approvals and proactive follow-up with authorities.
State FDA Approvals

  • Manage end-to-end approvals from State FDA, including:
    • Test Licenses
    • Manufacturing Licenses
    • Export & Domestic Licenses
    • COPP, FSC
    • Loan Licenses
    • WHO-GMP, State GMP/GLP certifications
CBN Regulatory Coordination

  • Liaise with Central Bureau of Narcotics (CBN) for:
    • Export Authorizations Import Authorizations
Cross-Functional Collaboration

  • Work closely with cross-functional teams (CFTs) including:
    • R&D
    • Quality Assurance / Quality Control
    • Manufacturing
    • Supply Chain & Logistics
    • Marketing
  • Ensure regulatory strategies are aligned and implemented effectively.
Regulatory Strategy in Product Development

  • Provide regulatory guidance during product development stages.
  • Define clear pathways for approvals in India and support global regulatory submissions.

Regulatory Strategy in Product Development

  • Provide regulatory guidance during product development stages.
  • Define clear pathways for approvals in India and support global regulatory submissions.

Regulatory Systems & Portals

  • Hands-on experience with regulatory portals:
    • SUGAM Portal
    • NSWS (National Single Window System)
    • IDML
    • IFP
    • Unified CBN Portal
Regulatory Query Management

  • Effectively handle and respond to queries raised by regulatory authorities.
  • Ensure timely and accurate submissions to avoid delays in approvals.

Communication & Stakeholder Management

  • Possess strong written and verbal communication skills.
  • Ability to coordinate with internal teams and external regulatory bodies efficiently.

Qualifications

B.Pharma with Six year of experience

About Us

Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.


Job Details

Role Level: Mid-Level Work Type: Full-Time
Country: India City: Ahmedabad ,Gujarat
Company Website: http://www.amneal.com Job Function: Legal & Compliance
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

Searching, interviewing and hiring are all part of the professional life. The TALENTMATE Portal idea is to fill and help professionals doing one of them by bringing together the requisites under One Roof. Whether you're hunting for your Next Job Opportunity or Looking for Potential Employers, we're here to lend you a Helping Hand.

Report

Disclaimer: talentmate.com is only a platform to bring jobseekers & employers together. Applicants are advised to research the bonafides of the prospective employer independently. We do NOT endorse any requests for money payments and strictly advice against sharing personal or bank related information. We also recommend you visit Security Advice for more information. If you suspect any fraud or malpractice, email us at abuse@talentmate.com.


Recent Jobs
View More Jobs
Talentmate Instagram Talentmate Facebook Talentmate YouTube Talentmate LinkedIn