Associate Mfg

Thousand Oaks, CA
Jul 23, 2021
Required Education
High School or equivalent
Position Type
Full time


Youve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge youve worked hard to acquire and the passion you already have. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.

Associate Manufacturing


What you will do

Lets do this. Lets 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)


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:
  • Bachelors degree OR Associates 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.

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 Plancomprising health, finance and wealth, work/life balance, and career benefitswith 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.


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.

Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

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 but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

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, or disability status.