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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.

Associate Manufacturing

Live

What you will do

Let’s do this. Let’s change the world. In this dynamic role you will collaborate with multiple functions within the Thousand Oaks site on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility. Responsibilities of the role include:

• Executing drug product filling and formulation activities, respectively

• Performing initial review of manufacturing batch records

• Maintaining a safe and compliant culture by identifying preventative measures

• Creating and/or revising standard operating procedures

• Leading continuous improvement initiatives, which may be cross-functional in nature

• Performing data analysis (e.g., SPC, CPV) of critical process parameters and making recommendations to Engineering and/or Process Development teams

• Developing finite schedule for tasks including, but not limited to unit operations

• Monitoring productivity and identifying countermeasures for issues impacting cycle time adherence

• Elevating critical and impactful events to management

• Utilizing appropriate systems for job duties (SAP, QMTS, and LIMS etc.)

• Supporting the introduction of new products and technologies into the facility

• Initiating and owning quality records, including but not limited to non-conformances (NC), Corrective/Preventative Actions (CAPA)

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Manufacturing professional we seek is a collaborative partner with these qualifications.

Basic Qualifications:

• Bachelor’s degree OR Associate’s degree and 4 years of Manufacturing experience OR High school diploma / GED and 6 years of Manufacturing experience

Preferred Qualifications:

• B.S. in a life science or related field

• 2 years of work experience in a GMP environment

• Ability to perform computer operations, such as ability to navigate in MS Office and Excel

• Ability to operate specialized equipment and computers as appropriate to the individual area

• Ability to adhere to regulatory requirements, written procedures and safety guidelines

• Ability to evaluate documentation/data according to company and regulatory guidelines

• Ability to interact with inspectors (internal and external)

• Technical writing capabilities

• Ability to organize work, handle multiple priorities and meet deadlines

• Demonstrated written and oral communication skills

• Presentation capabilities

• Detail oriented as well as flexible and adaptable to changing priorities and requirements.

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.

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