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Regulatory Affairs Manager - Devices

6+ years
Not Disclosed
10 April 9, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 Job Title: Regulatory Affairs Manager – Devices
 Location: Not specified (assumed India – JAPAC region)
 Work Location Type: Not specified (typically on-site or hybrid)
 Category: Regulatory


About Amgen

At Amgen, we believe in using the power of science and biotechnology to fight serious illnesses and serve patients around the world. With more than 10 million patients reached globally, Amgen is one of the world’s leading biotech companies, driven by the mission to serve patients and defy imagination.


Role Summary

In the role of Regulatory Affairs Manager – Devices, you will lead or support the development and execution of regulatory strategies for new and existing drug delivery devices and combination products in the JAPAC region. You will be instrumental in ensuring successful regulatory submissions, agency interactions, and sustainable regulatory processes.


Key Responsibilities

  • Support the development, communication, and maintenance of JAPAC regulatory strategic plans.

  • Lead or support regulatory agency engagements in the JAPAC region.

  • Lead or support filing activities and respond to related health agency inquiries.

  • Support device design control activities and review documentation.

  • Assess device-related standards/guidance for regulatory applicability and help form Amgen’s regional regulatory positions.

  • Perform regulatory assessments for change controls relevant to JAPAC.

  • Assist in the implementation and maintenance of internal regulatory processes.

  • Conduct device determination decisions for regulated items in the JAPAC region.

  • Participate in supplier engagement teams and due diligence efforts.

  • Review and provide regulatory input in development, quality, and supply agreements.

  • Support regulatory compliance initiatives and audits.


Basic Qualifications

  • Doctorate degree
    OR

  • Master’s degree and 2 years of pharma/biotech and/or medical device regulatory affairs experience
    OR

  • Bachelor’s degree and 4 years of pharma/biotech and/or medical device regulatory affairs experience


Preferred Qualifications

  • Master’s degree in Regulatory Affairs, Engineering, or Life Sciences

  • 6+ years of experience in medical device regulatory affairs

  • Experience with:

    • Design controls

    • Manufacturing and process development

    • Quality assurance/control

    • Analytical development

  • Regulatory submission experience for drug delivery or diagnostic devices

  • Regulatory CMC knowledge and experience

  • Strong project management and organizational skills

  • Excellent written and verbal communication

  • Familiarity with Veeva Vault platforms


Soft Skills

  • Leadership and self-motivation

  • Collaboration across cross-functional and international teams

  • Problem-solving mindset and regulatory foresight

  • Attention to detail and compliance mindset