Amgen - Regulatory Affairs Manager - CMC

Regulatory Affairs Manager (CMC)

- To facilitate product development and global registration by developing and executing regulatory strategies and effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle.

- The RA CMC Manager is responsible for execution and/ or coordination of global regulatory CMC activities, including providing leadership, guidance, and insight to oversee the successful execution and implementation of the regulatory strategy for an assigned set of commercial products.

- The RA CMC Manager is responsible for communicating the regulatory strategy, risks and issues to Regulatory and Operations senior management. The RA CMC manager coordinates communication, collaboration, and coordination with the site and regional CMC representatives within the department to develop and execute global regulatory activities.

- Contributes to product teams and acts as product lead or principal for one or more products. Provides strategic regulatory input and regulatory risk assessments for product teams; executes regulatory strategy with respect to preparation of submissions; complies with critical RA CMC processes; identifies need for process and strategy changes to meet internal Amgen initiatives and changes in external regulatory policy and guidance; reports needs for process changes to CMC systems and contributes to process improvements; incorporates changes in external regulatory guidance into CMC strategy and guidance for product teams; reports issues to RA CMC product team management.

Key Responsibilities Include:

- Generate and execute of global and country-specific regulatory strategies

- Provide CMC regulatory strategy for assigned projects by defining minimal regulatory filing requirements, submission strategy, and regulatory risk assessments

- Develop global dossiers for CMC content for initial submissions, variations and amendments- Support change management activities

- Develop response strategy and respond to health authority questions-

- Liaise with other functions in development, operations and commercial to ensure alignment of global regulatory strategies, timing, execution and supply plans

- Liaise with local regulatory teams to align on filing strategy

- Monitor and, as necessary, provide data to be entered into tracking systems for department deliverables and ensure information is current. Maintain submission information according to the Regulatory Information Management (RIM) system

- Follow established department regulatory processes to ensure cross-product alignment

- CMC- specific regulatory knowledge & experience-

- Doctorate degree OR Master's degree and 3 years of directly related experience OR Bachelor's degree and 5 years of directly related experience OR Associate's degree and10 years of directly related experience OR High school diploma / GED and12 years of directly related experience

- Experience in manufacture, testing (QC/QA or clinical), or distribution

- Regulatory CMC experience

Note : For your candidature to be considered on this job, you need to apply necessarily on the company's redirected page of this job. Please make sure you apply on the redirected page as well