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Regulatory Affairs Mgr

6-8 years
Not Disclosed
10 Dec. 14, 2024
Job Description
Job Type: Full Time Education: PhD/BSc/MSc/DPharma/PharmD/MBBS/BDS/BAMS/BHMS/MD 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

Here’s a refined and concise version of the Regulatory Affairs, CMC Submission Specialist job description for Amgen:


Position: Regulatory Affairs Specialist – Chemistry, Manufacturing, and Controls (CMC)

Department: Regulatory Affairs (RA CMC)
Location: Amgen India


About Amgen

At Amgen, we are dedicated to serving patients with serious illnesses through groundbreaking biotechnology. With a focus on Oncology, Inflammation, General Medicine, and Rare Disease, our innovations touch millions of lives each year.

Join our collaborative, innovative, and science-driven culture to transform lives while advancing your career.


Role Overview

Amgen’s Regulatory Affairs CMC team plays a key role in facilitating product development and global registrations by managing regulatory strategies and interactions. As part of the expanding ROOTS2 (Regulatory Optimization of Tactical and Strategic Support) team in India, you will support CMC submission execution across all development phases, modalities, and countries.

You will work closely with Amgen’s global teams to execute submission activities, manage projects, and maintain compliance with regulatory requirements.


Key Responsibilities

Submission Management:

  • Lead and execute submissions for annual reports, facility registrations, renewals, and product approvals.
  • Coordinate and prepare content for CMC submissions, including IND/CTAs, marketing applications, facility updates, postmarket variations, and annual notifications.
  • Oversee or manage team members, depending on experience level.

Document Coordination:

  • Interact with subject matter experts to deliver required CMC documentation.
  • Prepare and archive submission-related documents in the document management system.
  • Ensure compliance with country-specific requirements for CMC documents, including legalization processes.

Process & Team Support:

  • Develop and maintain process documents and conduct staff training on CMC procedures and systems.
  • Track and report project progress to teams and leadership.
  • Participate in cross-functional special projects to improve regulatory processes.

Qualifications

Basic Qualifications:

  • Doctorate + 1–3 years of experience in manufacturing, QA/QC, or regulatory CMC in the pharmaceutical/biotech industry, OR
  • Master’s + 4–6 years of relevant experience, OR
  • Bachelor’s + 6–8 years of relevant experience.

Preferred Qualifications:

  • Experience managing or mentoring team members.
  • Expertise in manufacturing, Process Development, QA/QC, or Analytical Development.
  • Comprehensive knowledge of regulatory CMC processes.
  • Proficiency in Veeva Vault platforms and mature project management skills.

Soft Skills:

  • Strong oral and written communication abilities.
  • Exceptional organizational and problem-solving capabilities.
  • Team-oriented mindset with a focus on meeting goals and timelines.

Why Join Amgen?

What We Offer:

  • Growth opportunities in a dynamic, inclusive, and global environment.
  • Competitive salary and comprehensive Total Rewards Plans, including health, career, and work-life benefits.

Impactful Work:

  • Contribute directly to the development of innovative therapies that improve patient outcomes.

Equal Opportunity Statement

Amgen is an Equal Opportunity Employer committed to fostering diversity and inclusion. We provide reasonable accommodations to individuals with disabilities throughout the hiring process and employment lifecycle.


Ready to Transform Lives?

Apply now to be part of a team that’s reshaping the future of healthcare.

Visit careers.amgen.com


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