Regulatory Affairs Manager
Regulatory Affairs Manager
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
- The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS) Company Core Safety Information (CCSI) and Reference Safety Information (RSI for assigned products including regulatory responsibilities in associated change control and labeling processes.
- This person is instrumental in the design development and maintenance of global regulatory processes and business solutions.
- This is a meaningful individual contributor who will partner with key business functional and business partners to ensure commercial objectives are achieved.
- Accountable for all operational aspects including owning creating and/or maintaining CCDS/CCSI/RSI documentation delivering maintaining and driving regulatory systems databases and labeling processes that support therapeutic and combination products.
- Lead the initial development approval and ongoing compliance of product labeling content throughout the product life cycle; track status and maintain documents in controlled process and systems workflows; lead reviews and manage the documents through approvals and governance by cross-functional executive and subject matter authority leadership.
- Make decisions regarding patient safety signals indications risk and other sophisticated change or regulated content creation/modification triggers.
- Support global implementation of CCDS/CCSI/RSI into country-specific labelling by developing and approving implementation of complex global and local labelling and other regulated solutions in accordance with the end-to-end regulated content labelling processes and commercial objectives including reviewing deviations exemptions and deferrals.
- Participate in the execution of regulatory labelling and content strategies for new products and ongoing compliance for products already on the market including monitoring evaluating and internally communicating new and existing applicable regulatory requirements.
- Lead or support global technology process and solution initiatives to standardize and enable standard process in labelling and content management including requirements use cases and translations.
- Deliver responses solutions and find opportunities to improve based upon quality initiatives including audits and risk mitigation.
- Perform gap analysis on regulated content management processes; design develop assess improve implement and maintain associated complex and simple Global Regulatory Affairs and Quality processes and business solutions.
- Bachelors degree in pharmacy biochemistry or similar science related field preferred.
- Minimum 5 years of pharmaceutical regulatory or regulated content management (e.g. labeling or Company Core Data Sheets) experience.
- Ability to run sophisticated projects and timelines in a matrix team environment.
- Strong project management and organizational skills.
- Ability to independently identify compliance risks and raise when necessary.
Employment Type
Full Time
