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Senior Manager - 2 at SUN PHARMA — Gurgaon

Experience13–18 yrs
SalaryNot disclosed
Work modeonsite
Posted29 Sept 2026

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About SUN PHARMA

SUN PHARMA is hiring in Gurgaon in pharma biotech. This role looks for around 13+ years of experience.

Skills

USFDA
CMC Module One
CMC Module Two
CMC Module Three
CMC Dossier Preparation
Lifecycle Management
eCTD Compilation
Regulatory Compliance
Cross-functional Collaboration

The role

A regulatory compliance manager at a pharmaceutical company prepares CMC Dossier Preparation and manages Lifecycle Management for USFDA submissions, applying Regulatory Compliance and eCTD Compilation. Cross-functional collaboration supports approvals and ongoing formulation changes.

Full job description

Job Title

Sr. Manager-2

Business Unit

Regulatory & Business Continuity

Job Grade

G9B

Location:

Gurgaon

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

Key Responsibilities

Regulatory submission of new products, variations, response to queries, Life cycle management for US and OAM region through preparation of quality dossiers enabling timely approvals.

Area Of Responsibility

New submissions:Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions.Review documents (Development report, scale up report, specification, stability protocol, analytical validation), etc. Before initiation of Exhibit batches for adequacy.Approval:Review & prepare response to deficiency enabling approval of products filed to regulatory agency.Lifecycle management for drug formulations:Prepare and review variation, Annual notification and labelling approval for US and OAMReview of change control and file variation as per country requirement Regulatory compliance:eCTD compilationEnsure reposition of comprehensive product information into central repositoryReview regulatory filing impact of variations, change controls, etc.

Competencies Required

Experience of USFDA market. Knowledge of CMC Module-1,2 & 3. CMC Dossier Preparation Lifecycle Management Cross-Functional Collaboration

Job Requirements

Educational Qualification –

M.Pharma

Experience –

Tenure : 13-18 Years

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).