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
- 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.
- 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 OAM
- Review of change control and file variation as per country requirement
- eCTD compilation
- Ensure reposition of comprehensive product information into central repository
- Review 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
