Job Description
Job Purpose:
The purpose of this role is to execute OTC regulatory activities for new products registrations and life-cycle maintenance for the portfolio of products defined by the US Business Units.
Must have OTC experience.
Key Responsibilities:
• Ensures cross portfolio aligned regulatory strategy to deliver timely approvals for US submissions and OTC Monograph product launches.
• Develop and implement regulatory strategies and documents for new product launches and maintenance of current products aligned with the regulations.
• Support key processes and ways of working, regulatory labelling and artwork review and aligned with local requirements.
• Support the development of claims/advertising and promotion within the regulations, ensuring risks are appropriately addressed and communicated.
• Prepares registration files...
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Submit ApplicationJob Details
- Location warren, nj
- Job Type Full-time
- Category Pharmaceutical Manufacturing
- Posted Date June 09, 2026
- Application Deadline July 19, 2026