Production Operations Group Lead - Day Shift

Takeda

Round Lake, Illinois, USA
Base: $71,800.00 - $112,860.00; bonus/equity: shor...
2-2-3 rotating schedule (day shift)
5+ years related experience or bachelor's degree
Cgmp and ehs regulatory compliance knowledge
Ability to work rotating night shifts and weekends
Takeda is seeking a Production Operations Group Lead for their Round Lake, Illinois facility, responsible for overseeing manufacturing processes and ensuring compliance with regulatory standards. The ideal candidate should have relevant experience in a regulated environment, strong leadership skills, and the ability to collaborate effectively across departments

Job Summary

  • This role supervises activities in initial inspection, pasteurization, and incubator production areas at the Round Lake facility.
  • The position requires ensuring manufacturing goals are achieved while maintaining strict compliance with cGMP, EHS, and FDA regulations.
  • Employees are eligible for a comprehensive benefits package including medical insurance, 401(k) match, and up to 120 hours of paid vacation.

Matching Summary

Match Score: 85

Takeda is seeking a Production Operations Group Lead for their Round Lake, Illinois facility, responsible for overseeing manufacturing processes and ensuring compliance with regulatory standards. The ideal candidate should have relevant experience in a regulated environment, strong leadership skills, and the ability to collaborate effectively across departments.

Salary

Base: $71,800.00 - $112,860.00; Bonus/Equity: Short-term and/or long-term incentives available; Benefits: Medical, dental, vision, 401(k), paid time off, tuition reimbursement

Skills & Requirements

Must-have

  • 5+ years related experience or bachelor's degree
  • cGMP and EHS regulatory compliance knowledge
  • Ability to work rotating night shifts and weekends
  • Proficiency in MS Word and Excel
  • Experience with FDA regulated environments preferred

Nice-to-have

  • Lean manufacturing principles application
  • Strong verbal and written communication skills
  • Collaborative team leadership approach
  • Process improvement project leadership
  • Troubleshooting support during deviations

Key Requirements

  • High School Diploma/GED with 5+ years experience OR Bachelor's degree with 2+ years
  • Understanding of cGMP and regulatory requirements
  • Willingness to work 2-2-3 rotating shift schedule
  • Ability to lift/push/pull up to 30 lbs
  • Experience in FDA regulated environment preferred

Work Rights

Not specified

Tailored Resume

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