hyderabad telangana cmc regulatory affairs Jobs – 6 Open Jobs Today

Regulatory Affairs Manager (CMC)
Amgen —Hyderabad, Telangana
- Bachelor's degree
- Quality control
- In-person
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Lonza —Hyderabad, Telangana
- Full-time
- English
- Project management
- Agile
Regulatory Affairs Senior Specialist
Lonza —Hyderabad, Telangana
- Full-time
- English
- Project management
- Agile
Senior Manager, Global Regulatory Affairs
DIFGEN PHARMACEUTICALS PRIVATE LIMITED —Kukatpally, Hyderabad, Telangana
- Full-time
- Master's degree
- Project management
- APIs
Team Leader, RA
AVEVA DRUG DELIVERY SYSTEMS INC —Kukatpally, Hyderabad, Telangana
- ₹13,00,000 - ₹20,00,000 a month
- Project management
- Communication skills
Associate Director, Commercial Tech Lead
DIFGEN PHARMACEUTICALS PRIVATE LIMITED —Kukatpally, Hyderabad, Telangana
- Manufacturing

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Regulatory Affairs Manager (CMC)

Amgen -
Hyderabad, Telangana

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Job details

Qualifications

Bachelor's degree
Quality control

Full job description

India - Hyderabad

JOB ID: R-244226 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: May. 11, 2026 CATEGORY: Regulatory

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 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

Knowledge and Skills

CMC- specific regulatory knowledge & experience

Education & Experience (Basic)

Bachelor’s degree and 8-13 years of directly related experience

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

Regulatory CMC experience

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cmc regulatory affairs jobs in hyderabad telangana

Regulatory Affairs Manager (CMC)

Regulatory Affairs Specialist

Regulatory Affairs Senior Specialist

Senior Manager, Global Regulatory Affairs

Team Leader, RA

Associate Director, Commercial Tech Lead

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