Sr Associate Regulatory Affairs - CMC in Uxbridge

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

What you will do

• In this vital role you will interface with the Amgen global, international, site and biosimilars Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) teams and the device team for specific strategies or activities that impact a product.
• You will be responsible for varying levels of product support, including leading projects, based upon your experience level.
• The 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.
• Contribute as a key member of the global regulatory CMC product team.
• Interact with authors/reviewers and subject matter experts with respect to delivery of regulatory documents required for regulatory submissions.
• Contribute to the organization and preparation of CMC investigational product amendments, post‐market supplements/variations, and new marketing applications.
• Document and archive CMC submissions and related communications in the document management system.
• Initiate and maintain CMC product timelines at the direction of product lead.
• Interface with the regulatory operations team.
• Train staff on select CMC procedures and systems.
• Provide report status of activities and projects to teams and department.
• Participate in cross-functional special project teams.

What we expect of you

• We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:
• Degree educated.
• Background in CMC related functions (e.g., Quality, Manufacturing, etc) with limited or no prior Regulatory Affairs experience.
• Curious, proactive, confident in tackling new challenges, and comfortable working collaboratively in a fast-paced learning environment.
• Developed project management and organizational skills.
• Strong and effective oral and written communication skills.

What you can expect of us

• As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.
• Vast opportunities to learn and move up and across our global organization.
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.
• Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.

LOCATION: Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a 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 an accommodation.