Regulatory Affairs Manager (Site)

Amgen Inc.

3.6

(9)

Hyderabad, India

Why you should apply for a job to Amgen Inc.:

  • 67% say women are treated fairly and equally to men
  • 78% would recommend this company to other women
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Flexible work models that empower staff members to work where and when they are most productive
  • Award-winning PTO plan and bi-annual company-wide shutdowns
  • With 11 Employee Resource Groups, 60 chapters & 11000 members everyone has opportunity to connect, network & foster a culture of belonging
  • #R-222937

    Position summary

    n teams on strategies and activities impacting licensed products.

    Roles & Responsibilities:

    Key responsibilities of the Regulatory Affairs Manager include:

      • Conducts periodic assessments of licenses / facilities and ensures business practices comply with current regulations and statutes.

      • Evaluates new and existing regulations to maintain up-to-date compliance.

      • Communicates requirements to internal Amgen functional teams.

      • Obtains supplemental documentation from internal and external partners.

      • Prepares, reviews, and submits license applications and renewals.

      • Maintains all State Licensing documentation, submissions, and interactions with State Authorities.

      • Interfaces with State Board of Pharmacy (BoP) and/or Department of Health (DoH).

      • Completes required annual notifications to U.S. FDA

      • Obtains DUNS and FEI numbers for new U.S. sites, as required

      • Processes Financial obligations relating to fee payment.

      • Identifies and implements process improvements for the state licensing process

      • Coaches and supports junior regulatory staff's career development

    What we expect of you

    We are all different, yet we all use our unique contributions to serve patients. The successful candidate will have the following qualifications:

    Basic Qualifications:

    • Doctorate degree OR

    • Master's degree and 3 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR

    • Bachelor's degree and 5 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry

    Preferred Qualifications:

    • Degree in Life Science discipline

    • Regulatory CMC specific knowledge & experience

    • Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry

    • Working knowledge of US state and/or federal licensing requirements

    What you can expect of us

    As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.

    In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

    Apply now

    for a career that defies imagination

    Objects in your future are closer than they appear. Join us.
    careers.amgen.com

    .

    Why you should apply for a job to Amgen Inc.:

  • 67% say women are treated fairly and equally to men
  • 78% would recommend this company to other women
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Flexible work models that empower staff members to work where and when they are most productive
  • Award-winning PTO plan and bi-annual company-wide shutdowns
  • With 11 Employee Resource Groups, 60 chapters & 11000 members everyone has opportunity to connect, network & foster a culture of belonging