Lead GMP Manufacturing Technician

USA - 3390 Baxalta U.S., Inc.

Round Lake (IL)

On-site

USD 40,000 - 63,000

Full time

2 days ago
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Job summary

Takeda is seeking a Lead Manufacturing Technician in Round Lake, IL to drive floor operations, ensure aseptic practices, and maintain strict cGMP compliance. You will lead scheduling, material management, and cross-functional collaboration to implement process changes and continuous improvement.

The role emphasizes safety, documentation integrity, and staff development while supporting tech transfer and GMP-driven investigations.

Qualifications

  • 6+ years of related industry experience or an associate degree with 5+ years GMP manufacturing experience.
  • Experience in manufacturing lead, team support, or coordination roles preferred.
  • Proficiency with aseptic techniques and cleanroom manufacturing practices.

Responsibilities

  • Serve as primary contact for troubleshooting and escalation.
  • Coordinate daily scheduling, staffing, and real-time staff assignments.
  • Oversee routine and critical manufacturing operations, including commissioning and changeover/validation.
  • Ensure documentation complies with cGMP and good documentation practices.
  • Manage floor inventory and material deliveries.
  • Promote safe and compliant operations and raise safety concerns as needed.
  • Support continuous improvement with visual management and ergonomic enhancements.
  • Provide team leadership through training, coaching, and performance feedback.
  • Support quality systems with deviations, investigations, and CAPAs.
  • Collaborate with QA, engineering, facilities, and operations to resolve issues and support tech transfer.

Skills

GMP manufacturing
Leadership
Aseptic technique
cGMP knowledge
Scheduling

Education

High school diploma + 6+ years
Associate degree in life sciences/engineering

Tools

SAP
LIMS
TrackWise

Job description

Takeda is seeking a Lead Manufacturing Technician in Round Lake, IL to drive floor operations, ensure aseptic practices, and maintain strict cGMP compliance. You will lead scheduling, material management, and cross-functional collaboration to implement process changes and continuous improvement.

The role emphasizes safety, documentation integrity, and staff development while supporting tech transfer and GMP-driven investigations.

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