Manager QA
Amgen
This listing was originally posted on Amgen's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moIf 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 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 as:
Manager QA
At Amgen Breda, medicines are labeled, assembled, stored, and eventually shipped to various countries worldwide. Every day more than 1000 people from 38 different nationalities are working on supply chain processes, manufacturing, marketing, and sales of our medicines and clinical research into new medicines.
LIVE
What you will do
Being in this role at the Quality team, you will be responsible for leading and directing Quality staff supporting production in the shift, including managing their performance and supporting their development.
The Manager QA is also responsible for providing guidance and direction to Production, Maintenance & Engineering, and Quality staff regarding compliance with quality standards and procedures. Optional, but not a requirement, you will be fulfilling the duties as a Qualified Person.
Let’s do this. Let’s change the world.
In this vital role, you will:
WIN
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The Manager QA professional we seek is a team leader with these qualifications:
• Master in Science degree in Pharmacy or equivalent; OR any other Master’s degree education supplemented with relevant Pharmaceutical GMP experience.
• Previous practical experience in processes involved in clinical and commercial manufacturing (GMP), warehousing, supply chain, equipment engineering principles, and validation; Typically 2+ years of related professional experience.
• Optional, but not mandatory: knowledgeable and skilled to fulfill the requirements of EU directive 2001/83/EC article 49 (Qualified Person) and GDP guidelines 2013/C 68/01 chapter 2.2 (Responsible Person). The least requirement is to have thorough knowledge about these processes, but it is not a requirement to execute.
• Ability to problem solve and make scientific risk-based decisions;
• Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with the ability to effectively communicate and collaborate with production and technical staff.
THRIVE
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.
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