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Amgen Inc
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Regulatory Affairs Sr Associate (Site)

Regulatory Affairs Sr Associate (Site)

Amgen Inc

2 - 7 years

4 - 9 Lacs

hyderabad

Posted:8 hours ago| Platform:

Apply

Skills Required

supply chain qa qc pharma pharmacy qaqc cmc regulatory compliance licensing operations

Work Mode

Work from Office

Job Type

Full Time

Job Description

Career Category Regulatory Job Description

R egulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The Regulatory Compliance team is a part of RA CMC and is seeking to expand its capacity in India . The Regulatory Compliance team performs assessment of operational changes for regulatory reportability and maintenance of state and federal licenses for Amgen products across phases of development, modality, and countries.

The team member will be responsible for maintaining U.S. state and federal commercial product licenses and will collaborate with Global CMC, Site CMC, and Device Regulatory, Operations, Quality, and Supply Chain teams on strategies and activities impacting licensed products.

Roles & Responsibilities:

Key responsibilities of the Regulatory Sr Associate include:

- Tracks license status to ensure all are current and effective.
- 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 ).
- Complete s required annual notifications to FDA

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a type of person with these qualifications.

Basic Qualifications:

Master s degree OR
Bachelor s degree and 2 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR
Associate s degree and 6 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

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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Regulatory Affairs Sr Associate (Site)