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Regulatory Affairs Mgr

7+ years
Not Disclosed
10 May 1, 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

Location: India – Hyderabad (On Site)
Job ID: R-207691
Date Posted: April 8, 2025
Category: Regulatory
Company: Amgen


Job Summary

Amgen, a leading biotechnology company, is seeking a Regulatory Affairs Manager to join the Regulatory Optimization of Tactical and Strategic Support (ROOTS2) team. This team plays a pivotal role in supporting CMC (Chemistry, Manufacturing, and Controls) and Device submissions for Amgen products across global markets and product development stages. As a Regulatory Affairs Manager, you will drive regulatory submission execution, lead projects, and ensure compliance with regulatory requirements.


Key Responsibilities

  • Lead the submission process for annual reports, facility registrations, facility renewals, and product renewals

  • Oversee and manage staff, providing training and onboarding

  • Coordinate and prepare CMC submission content plans including IND/CTAs, IDE/PSA, new marketing applications, facility registrations, and more

  • Interact with subject matter experts and cross-functional teams for the preparation of regulatory submission documents

  • Manage product timelines for CMC and/or Device submissions

  • Maintain documentation of CMC and Device submissions and related communications

  • Participate in cross-functional project teams and communicate project statuses

  • Provide training on CMC procedures and systems to staff


Required Skills and Experience

  • Doctorate degree OR

  • Master’s degree with 5+ years of experience in regulatory CMC or QA/QC in the Pharmaceutical/Biotechnology industry

  • Bachelor’s degree with 7+ years of experience in manufacturing, QA/QC, or regulatory CMC

  • Strong experience in project management and staff management

  • Proficient in Veeva Vault and other relevant regulatory tools


Preferred Qualifications

  • BS degree in Life Science

  • Experience managing staff and overseeing regulatory submission processes

  • Knowledge in IVD, Device, or Combination Product regulatory submissions

  • Strong organizational, communication, and problem-solving skills


Why Join Amgen?

  • Impactful work: Help shape the future of biopharmaceutical products and ensure regulatory compliance across global markets

  • Collaborative culture: Join a dynamic team where innovation, growth, and diversity are prioritized

  • Competitive benefits: Comprehensive benefits package with opportunities for career advancement


How to Apply

Visit: careers.amgen.com