Assistant Manager
AssistantManager-RA
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“Assistant Manager - RA at Assistant Manager. Skills: Regulatory Affairs, Dossier compilation, HA submissions, Regulatory compliance. Lead compilation and submission of regulatory dossiers for new drugs, line extensions, additional indications, and lifecycle changes (renewals, site registrations, production transfers). Manage Clinical Trial Application (CTA) submissions and ensure compliance throughout study lifecycle”
What They're Looking For.
Must Have
Bachelor’s degree in Pharmacy / Life Sciences / Health Sciences/ Chemistry, 5 + years of hands-on experience in Regulatory Affairs within Indian regulatory framework, preferably in a multinational pharmaceutical environment, experience in dossier compilation and HA submissions (NDAs, CTAs, lifecycle management), Good understanding of Indian regulatory requirements (e.g. , CDSCO processes, clinical trial regulations, post-approval compliance), cross-functional collaboration and stakeholder management skills, Effective communication (written and verbal) and interpersonal skills
Nice to Have
Post-graduate degree in Pharmacy / Life Sciences / Regulatory Affairs/ Chemistry, Exposure to global regulatory environments or working with HQ/overseas teams, Experience in regulatory strategy planning for new product launches
What You'll Do.
Lead compilation and submission of regulatory dossiers for new drugs
additional indications
and lifecycle changes (renewals
production transfers)
Manage Clinical Trial Application (CTA) submissions and ensure compliance throughout study lifecycle
Support development and execution of regulatory strategies for pipeline products to enable timely market access
Ensure timely execution of post-approval regulatory commitments including PSURs
Drive regulatory compliance tracking
including monitoring submissions
and ongoing obligations with Health Authorities
Support critical regulatory changes (e. g.
supply chain changes) with minimal disruption to business
Ensure data integrity and compliance through maintenance of regulatory databases and audit readiness
Drive process improvements
and compliance oversight to enhance regulatory efficiency and inspection readiness
How You'll Work.
Team & Collaboration
Collaborate with cross-functional stakeholders (Legal, QA, Supply Chain, Global teams) to ensure seamless regulatory execution and supply continuity
Communication Scope
Effective communication (written and verbal)
Full Job Description
**Job Description Summary** Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify and maintain records. Interprets & enforces all documentation formatting, standards, policies, and operating procedure requirements. May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers. May analyze and evaluate data, extract pertinent information, prepare information abstracts and executive summaries of material searched. May maintain extensive knowledge of product information and continuous contacts with local, regional, and divisional customers. **Job Description** **Key Responsibilities** * Lead compilation and submission of regulatory dossiers for new drugs, line extensions, additional indications, and lifecycle changes (renewals, site registrations, production transfers). * Manage Clinical Trial Application (CTA) submissions and ensure compliance throughout study lifecycle. * Support development and execution of regulatory strategies for pipeline products to enable timely market access. * Ensure timely execution of post-approval regulatory commitments including PSURs, CMC variations, and labeling updates. * Drive regulatory compliance tracking, including monitoring submissions, approvals, and ongoing obligations with Health Authorities. * Collaborate with cross-functional stakeholders (Legal, QA, Supply Chain, Global teams) to ensure seamless regulatory execution and supply continuity. * Support critical regulatory changes (e.g., site changes, legal entity updates, supply chain changes) with minimal disruption to business. * Contribute to regulatory intelligence gathering and provide guidance on evolving regulatory
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