Associate Manufacturing (swing Shift 2pm-11pm)

Amgen UK

Thousand Oaks, California, United States
Base: $70,985.20 - $96,038.80 usd annually; bonus:...
Swing shift (2pm-11pm)
Bachelor's degree or equivalent experience
Gmp/gdp regulatory compliance knowledge
Manual visual inspection of drug products
Amgen UK is seeking an Associate Manufacturing professional for their Thousand Oaks facility, focusing on drug product manual inspections, batch record reviews, and continuous improvement initiatives. The role requires collaboration with multiple functions and adherence to GMP standards, offering a dynamic workplace culture

Job Summary

  • This role supports Amgen's mission to serve patients living with serious illnesses by manufacturing innovative medicines.
  • The successful candidate will perform manual visual inspections, review batch records, and lead continuous improvement initiatives within a dynamic environment.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, and flexible work models to support professional growth.

Matching Summary

Match Score: 85

Amgen UK is seeking an Associate Manufacturing professional for their Thousand Oaks facility, focusing on drug product manual inspections, batch record reviews, and continuous improvement initiatives. The role requires collaboration with multiple functions and adherence to GMP standards, offering a dynamic workplace culture.

Salary

Base: $70,985.20 - $96,038.80 USD annually; Bonus: Discretionary annual bonus program available; Benefits: Comprehensive health, dental, vision, retirement plan, and stock-based incentives included

Skills & Requirements

Must-have

  • Bachelor's degree or equivalent experience
  • GMP/GDP regulatory compliance knowledge
  • Manual visual inspection of drug products
  • Batch record review and documentation
  • SAP, QMTS, and LIMS system usage

Nice-to-have

  • Continuous improvement initiative leadership
  • Cross-functional collaboration skills
  • Data analysis using SPC and CPV methods
  • Technical writing capabilities
  • Ability to present to management

Key Requirements

  • Bachelor's degree OR Associate's degree with 6 months GMP experience
  • High school diploma with 2 years GMP experience
  • Experience in a GMP environment preferred
  • Proficiency in MS Office and Excel required

Work Rights

Not specified

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