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Associate Manufacturing - Swing Shift Midnight

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Amgen Inc. (IR)
Full Time position
Listed on 2026-01-31
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering, Manufacturing Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 75618 - 89473 USD Yearly USD 75618.00 89473.00 YEAR
Job Description & How to Apply Below
Position: Associate Manufacturing - Swing Shift (1pm - Midnight)
##
** Career Category
** Manufacturing## ##
** Job Description
** Join Amgen’s Mission of Serving Patients 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** **(Swing Shift)
**** What you will do
** Let’s do this! Let’s change the world! In this dynamic role, you will be an Associate in the manufacturing organization at Amgen Thousand Oaks (ATO). The initial schedule will be 10 hours shift Mon to Thursday or Tuesday to Friday. Associates will be completing operations on the floor in our manufacturing services, upstream area and are responsible for the manufacturing of cGMP (Current Good Manufacturing Practices) drug substance.

With general direction, the Associate will support all floor operations in accordance with cGMP practices.
*
* Please note:

** no relocation assistance will be provided for this position.
** Responsibilities will include...
**** Compliance:
*** Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance
* Assure proper gowning and aseptic techniques are always followed
** Process/Equipment/Facilities:
*** Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment and assigned area
* Run and monitor critical process tasks per assigned procedures
* Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records [EBRs])
* Complete washroom activities: cleaning equipment, small to large scale, used in production activities
* Identify and raise issues and concerns regarding daily routine functions related to process and tasks; may engage with team on potential solutions
* Perform documentation for assigned functions (i.e., equipment logs, EBRs)
* Collaborate as part of a cross-functional team (i.e., QA/QC, F&E (Facilities & Engineering), PD (Process Development), Regulatory, etc.) in completing production activities
** What we expect of you
** We are all different, yet we all use our unique contributions to serve patients. The hard-working professional we seek is a standout individual with these qualifications.
*
* Basic Qualifications:

*** Bachelor's degree Or
* Associate's degree and 6 months of biotech or pharmaceutical manufacturing, process development or quality experience Or
* High School diploma/GED and 2 years of biotech or pharmaceutical manufacturing, process development or quality experience
*
* Preferred Qualifications:

*** Experience in a regulated industry such as biotechnology or pharmaceutical
* Basic understanding and process experience in a cGMP manufacturing facility
* Excellent verbal and written communication
* Proficient Microsoft Office skills, and knowledge of other electronic systems such as E /MES, Delta V, and Electronic Quality Systems
* An ability to demonstrate desire and drive to learn and grow their understanding of operations and processes
** 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…
Position Requirements
10+ Years work experience
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