Company

RegulatoryAffairsManager(CMC)

Madurai, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Regulatory Affairs Manager (CMC). Skills: Regulatory Affairs (CMC), Regulatory Strategy, Dossier Development, Health Authority Interactions. Execution and/or coordination of global regulatory CMC activities. Providing leadership, guidance, and insight to oversee the successful execution and implementation of the regulatory strategy for an assigned set of commercial products”

Industry & Context.

Problems you'll solve

Regulatory risk assessments; Responding to health authority questions

What They're Looking For.

Must Have

CMC- specific regulatory knowledge & experience, 3 years of directly related experience (with Master's degree), 5 years of directly related experience (with Bachelor's degree), Experience in manufacture, testing (QC/QA or clinical), or distribution, Regulatory CMC experience

What You'll Do.

Execution and/or coordination of global regulatory CMC activities

and insight to oversee the successful execution and implementation of the regulatory strategy for an assigned set of commercial products

Communicating the regulatory strategy

risks and issues to Regulatory and Operations senior management

Coordinating communication

and coordination with the site and regional CMC representatives within the department to develop and execute global regulatory activities

Contributing to product teams and acting as product lead or principal for one or more products

Providing strategic regulatory input and regulatory risk assessments for product

Executing regulatory strategy with respect to preparation of regulatory filings

Identifying need for process and strategy changes to meet internal Amgen initiatives and changes in external regulatory policy

Reporting needs for process changes to CMC systems

Contributing to process improvements

Incorporating changes in external regulatory guidance into CMC strategy and guidance for product

Reporting issues to RA CMC product team management

Generating and executing of global and country-specific regulatory strategies

Providing CMC regulatory strategy for assigned projects by defining minimal regulatory filing requirements

and regulatory risk assessments

Developing global dossiers for CMC content for initial submissions

variations and amendments

Supporting change management activities

Developing response strategy and responding to health authority questions

Liaising with other functions in development

operations and commercial to ensure alignment of global regulatory strategies

execution and supply plans

Liaising with local regulatory teams to align on filing strategy

providing data to be entered into tracking systems for department deliverables and ensuring information is current

Maintaining submission information according to the Regulatory Information Management (RIM) system

Following established department regulatory processes to ensure cross-product alignment

How You'll Work.

Team & Collaboration

Contributes to product teams; Coordinates communication, collaboration, and coordination with the site and regional CMC representatives; Liaises with other functions in development, operations and commercial; Liaises with local regulatory teams

Communication Scope

Communicating the regulatory strategy, risks and issues to Regulatory and Operations senior management; Coordinates communication; Communicating regulatory strategy

Process & Methodology

Oversee the successful execution and implementation of the regulatory strategy, Develop and execute global regulatory activities, Acts as product lead or principal for one or more products, Manage submission information

Full Job Description

## **Career Category** Regulatory ## ## **Job Description** 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. **Key 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

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