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Associate Manufacturing - Thousand Oaks CA

VetJobs
Thousand Oaks, CA Full Time
POSTED ON 3/29/2026
AVAILABLE BEFORE 4/26/2026
Job Description

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Associate Manufacturing

What you will do

Responsibilities

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 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

Applying 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)

Auto req ID

468672BR

Minimum Education Required

High School/GED

Job_Category

Manufacturing

Additional Qualifications/Responsibilities

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 6 months of Manufacturing and/or Operations experience OR High school diploma / GED and 2 years of Manufacturing and/or Operations 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.

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In Addition To The Base Salary, Amgen Offers a Total Rewards Plan, Based On Eligibility, Comprising Of Health And Welfare Plans For Staff And Eligible Dependents, Financial Plans With Opportunities To Save Towards Retirement Or Other Goals, Work/life Balance, And Career Development Opportunities That May Include

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts

A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

Stock-based long-term incentives

Award-winning time-off plans

Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Salary Range

75,618.00 USD - 89,473.00 USD

City*

Thousand Oaks

State*

California

Job Code

Pharmaceutical Pharmaceutical

Affiliate Sponsor

Amgen

Salary Range

$75,000-$100,000

Salary : $75,000 - $100,000

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