Lead Manufacturing Technician – cGMP & Process Optimization

Takeda

Round Lake (IL)

On-site

USD 30,000 - 47,000

Full time

8 days ago

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Job summary

Takeda is seeking a Manufacturing Technician III in Round Lake, IL. This role involves executing production processes with strict adherence to cGMP, safety, and quality guidelines. You will troubleshoot, lead hands-on production activity, and assist in new procedures or technology transfers as needed.

You will manage paperwork per GDP/GMP, train peers, and participate in continuous improvement initiatives while supporting multiple shifts on a 2-2-3 schedule.

Qualifications

  • Must have 4+ years of related work experience or AA degree or higher with 2+ years of related work experience.
  • English language proficiency in reading, writing and following detailed instructions.
  • Good interpersonal skills and ability to work in a team.
  • Strong understanding of cGMP regulations.
  • Familiarity with pharmaceutical production equipment including autoclave, DP oven and CIP/SIP.

Responsibilities

  • Execute production processes following cGMP and safety guidelines.
  • Troubleshoot process & equipment problems to minimize downtime.
  • Lead hands-on production activities under supervision and rewrite procedures as needed.
  • Complete relevant paperwork following GDP/GMP guidelines.
  • Participate on Continuous Improvement Teams.
  • Prepare the next shift for success and coordinate with maintenance/metrology for preventive maintenance.

Skills

Troubleshooting
Production ops
cGMP compliance
Team leadership
Documentation

Education

High school diploma or GED
AA/AS degree or higher

Tools

JDE
ERP systems
Autoclave
DP oven
CIP/SIP

Job description

Takeda is seeking a Manufacturing Technician III in Round Lake, IL. This role involves executing production processes with strict adherence to cGMP, safety, and quality guidelines. You will troubleshoot, lead hands-on production activity, and assist in new procedures or technology transfers as needed.

You will manage paperwork per GDP/GMP, train peers, and participate in continuous improvement initiatives while supporting multiple shifts on a 2-2-3 schedule.

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