Assistant Manager

Glenmark Pharmaceuticals; Thane; On-site; INR 1,200,000 - 2,000,000; Full time

Job summary

Glenmark Pharmaceuticals in Navi Mumbai invites a seasoned regulatory affairs professional for the role of Assistant Manager in Global Regulatory Affairs. Based at Mahape, Navi Mumbai, you will drive regulatory submissions across EU and Canada, ensuring compliance and timely filing.

You will coordinate with cross-functional teams, prepare dossiers, and respond to agency queries, while maintaining meticulous traceability of activities. A 9–12 year background in regulatory submissions is essential.

Qualifications

• Must have 9–12 years of Regulatory Affairs experience (EU, US/CA markets).
• Experience in dossier submissions of drug products for regulated markets.
• Educational qualifications include M. Pharmacy (Pharmaceutics) and regulatory certifications.

Responsibilities

• Meet pre-requisites of Health Agencies and perform pre-submission due diligence (EU/Canada).
• Provide regulatory inputs in developmental activities at early product development stages.
• Coordinate with stakeholders for data requirements and dossier compilation in EU/Canada.
• Compile, review and submit MA applications to Europe and ANDS to Health Canada per guidelines.

Skills

Regulatory submissions

Dossier compilation

EU/Canada regulatory knowledge

Time management

Teamwork

Independent work

Education

M. Pharm (Pharmaceutics)

Regulatory Certification

Job description

Designation: Assistant Manager

Business Unit: Research & Development

Function: Global Regulatory Affairs

Office Location: Mahape, Navi Mumbai

Position description: To ensure regulatory submissions in various geographical areas like EU and Canada.

Primary Responsibilities:

• To meet the pre-requisites of respective Health Agencies and perform pre-submission due diligence where required (eg. EU/Canada where dossier extension from US approved portfolio is done).
• Participation and provision of regulatory inputs in developmental activities at initial stages of product development.
• To co-ordinate with various stakeholders for data requirements for review and dossier compilation in EU and Canada in accordance with updated regulatory guidance for the respective markets.
• Compilation, review and submission of marketing authorization (MA) application to Europe market and abbreviated new drug submission (ANDS) to Health Canada ensuring they are in conformance with applicable regulatory guidelines and that the highest quality of standards are met.
• Review and submit responses to queries (RTQ), clarifax (NON) received from the regulatory authorities within stipulated timelines
• Support to business for Consolidated Pre-approved dossiers and timely response to deficiencies for Out Licensing Partners for EU market.
• Tracking of Canadian Deficiency trends in order to establish a proactive approach during dossier filing.
• Database maintenance for easy traceability of activities performed.

Educational qualifications preferred

M. Pharmacy (Pharmaceutics) ; Regulatory Certification .

Required work experience

• 9-12 years in Regulatory Affairs (EU, US/ CA Markets)
• Experience in dossier submission of drug products for regulated markets.

Required Knowledge & Skills :

Functional / Technical

• Expertise in technical review of submission documents and compilation of dossier as per Agencys expectation, which will lead to minimize queries from health agency.
• Time management abilities, working well under pressure, self-motivated, strong work ethic, Flexibility/adaptability

Behavioural Attributes

• Team work, positive approach in work, time management
• Ability to work independently

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