Specialist QA
AmgenUs - rhode island - west greenwichUpdate time: January 27,2022
Job Description

Career Category

Quality

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. 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, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.

Specialist QA

Live

What you will do

Let’s do this. Let’s change the world. In this vital role you will provide high complexity tactical support to Site Leads across multiple Quality Systems and Processes.

  • Perform tactical batch disposition activities in support of lot release

  • Lead and own NC, CAPA and Change Control records for External Supply Quality

  • Lead and drive Quality records to closure independently

  • Provide tactical information to the networks (i.e., metrics to QMR, MR, data verification, trending, periodic monitoring, APR)

  • Call out risks or roadblocks to management

  • Drive timely decision making using DAI principles

  • Drive continuous improvements and Amgen first mentality

  • Train on required Quality Systems (NCMS, CCMS, LIMS, SAP, and others as applicable)

Authority

  • Own Quality record content

  • Proposes revisions to SOPs in area of responsibility

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek will have these qualifications.

Doctorate degree

OR

Master’s degree and 3 years of directly related experience

Or

Bachelor’s degree and 5 years of directly related experience

Or

Associate’s degree and 10 years of directly related experience

Or

High school diploma / GED and 12 years of directly related experience

Preferred Qualifications:

  • 4+ years of quality and manufacturing experience in biotech or pharmaceutical industry

  • Bachelor’s Degree in a Science Field

  • cGMP Experience

  • Ability to lead all aspects of multiple projects simultaneously

  • Able to successfully lead workload to timelines

  • Familiarity with basic project management tools

  • Ability to negotiate a position after taking feedback from multiple sources

  • Proven ability to consistently deliver timely, and high-quality results

  • Ability to operate in a matrixed or team environment

  • Understanding of the applicable manufacturing/testing processes (i.e. API, Drug Substance, Drug Product, Packaging, Device manufacturing processes)

  • Ability to travel +/- 10% of time to domestic and international Amgen sites

  • Remote work availability

Thrive

Some of the vast rewards of working here

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.

  • Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey

  • A 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—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor

Apply now

for a career that defies imagination

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

careers.amgen.com

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