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Regulatory Affairs Mgr

5-7 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 (RA CMC)

Department:

Regulatory

Company:

Amgen

Location:

Hyderabad, India

Work Location Type:

On Site

Date Posted:

April 8, 2025

Application Deadline:

Not specified

Job ID:

R-207691


Job Summary:

Amgen is hiring a Regulatory Affairs Manager in Regulatory Affairs – Chemistry, Manufacturing and Controls (RA CMC). The role is part of the ROOTS2 (Regulatory Optimization of Tactical and Strategic Support) team, which supports global regulatory submission execution across the product lifecycle and modalities. The role includes project leadership, regulatory strategy execution, and direct interaction with global and site-based RA CMC teams.


Key Responsibilities:

  • Lead regulatory submissions for:

    • Annual reports

    • Facility registrations/renewals

    • Product renewals

  • Potential oversight or management of junior staff

  • Act as a key contact for submission execution or reporting activities

  • Develop and maintain regulatory process documentation

  • Train and onboard new team members

  • Coordinate with cross-functional teams and SMEs for CMC documentation

  • Prepare/oversee CMC submission content plans:

    • IND/CTAs, IDE/PSA/CIA, marketing applications, post-market supplements, Module 3 baselines, annual reports

  • Manage CMC country-specific documents and legalization

  • Document and archive submissions in document management systems

  • Initiate and maintain timelines for CMC/Device submissions

  • Interface with regulatory operations and cross-functional teams

  • Participate in special project teams and status reporting


Basic Qualifications:

One of the following:

  • Doctorate degree OR

  • Master’s degree + 5 years in manufacturing, QA/QC, or regulatory CMC (Pharma/Biotech) OR

  • Bachelor’s degree + 7 years in manufacturing, QA/QC, or regulatory CMC (Pharma/Biotech)


Preferred Qualifications:

  • BS degree in Life Sciences

  • Experience managing or mentoring staff

  • Experience in:

    • Manufacturing

    • Process Development

    • Quality Assurance/Control

    • Analytical Development

  • Regulatory submission experience in IVD, Device, or Combination Products

  • Strong Regulatory CMC knowledge

  • Project management and organizational skills

  • Effective written and verbal communication

  • Experience using Veeva Vault platforms


About Amgen:

Amgen is a Fortune 500 biotechnology company with over 40 years of scientific innovation. It serves millions of patients globally and is committed to advancing medicine and transforming lives. The company fosters a collaborative, inclusive, and science-driven culture.