Process Engineer Ii

Takeda

Thousand Oaks, CA, USA
Base: $70,000.00 - $110,000.00; bonus/equity: elig...
Process engineering support
Manufacturing operations in gmp environment
Equipment troubleshooting and investigations
The Process Engineer II independently supports moderately complex engineering activities, drives process improvements, and partners cross-functionally to ensure safe, compliant, and efficient manufacturing operations

Job Summary

  • The Process Engineer II independently supports moderately complex engineering activities, drives process improvements, and partners cross-functionally to ensure safe, compliant, and efficient manufacturing operations.
  • Takeda offers a patient-focused, inclusive, and collaborative workplace committed to delivering better health and a brighter future globally.
  • U.S. based employees may be eligible for medical, dental, vision insurance, 401(k) plan with company match, disability coverage, life insurance, tuition reimbursement, paid volunteer time off, company holidays, sick time, and paid vacation.

Matching Summary

The Process Engineer II independently supports moderately complex engineering activities, drives process improvements, and partners cross-functionally to ensure safe, compliant, and efficient manufacturing operations.

Salary

Base: $70,000.00 - $110,000.00; Bonus/Equity: Eligible for short-term and/or long-term incentives; Benefits: Medical, dental, vision, 401(k), disability, life insurance, tuition reimbursement, paid time off

Skills & Requirements

Must-have

  • Process engineering support
  • Manufacturing operations in GMP environment
  • Equipment troubleshooting and investigations
  • Process improvement projects
  • Use of engineering tools like FMEA and Design of Experiments
  • Compliance with cGMP and Good Engineering Practices

Nice-to-have

  • Strong technical writing skills
  • Cross-functional collaboration
  • Ability to manage multiple assignments
  • Presentation of technical information
  • Sound judgment and integrity

Key Requirements

  • B.S. in Engineering required
  • Minimum 3 years GMP pharmaceutical or biotechnology experience
  • 5 years preferred experience in regulated manufacturing
  • Experience supporting manufacturing operations and capital projects
  • Knowledge of cGMP manufacturing and Good Engineering Practices

Work Rights

Not specified

Tailored Resume

Cover Letter