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Job Description

About the role:

As a Manufacturing Technician II, you will implement all processes in production while strictly following cGMP, environmental health and safety guidelines and any applicable related regulations. You will have technical and administrative competence to organize and lead production activities. You will participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include assisting with the movement of Flexbumin between the different stages of inspection to packaging within the value stream. In this role, you may act as line lead, and will ensure the line operates smoothly and keeps up with daily goals. In addition, you will document your process activities on routers or in the electronic batch management system (EBM). You will report to the Supervisor, Manufacturing. The role supports Takeda's mission by ensuring efficient and high-quality production processes.

How you will contribute:

• Maintain a safe and quality working environment

• Participate in Continuous Improvement Teams.

• Support manufacturing operations.

• Lead Manufacturing Technicians I in daily tasks.

• Operate general production equipment (such as Downstream Automated Packaging {DAP} lines, forklifts, and hoists).

• Move pallets to different rooms within the value stream.

• Communicate and work cross-functionally with other departments.

• Receive and distribute supplies into the production area.

• Follow cGMP, environmental health and safety guidelines, and any other regulations.

• Complete relevant paperwork and electronic system prompts/tasks, following GDP/GMP guidelines.

• Perform daily cleaning of the production area to maintain in GMP fashion.

• Train new and existing employees/contractors on procedures.

• Communicate issues related to safety, quality, compliance and equipment to the manufacturing lead operator and supervisor.

• May perform other duties as assigned to enable team success and contribute toward professional development.

What you bring to Takeda:

​Education & Experience:

• High school diploma or GED with 2+ years of relevant experience, or Associate degree with 1+ year in a cGMP-regulated manufacturing or packaging environment.

Technical Skills:

• Proficient in operating and troubleshooting equipment (e.g., DAP lines, forklifts, hoists).

• Familiarity with cGMP, GDP, and electronic batch management systems.

• Experience handling and moving pharmaceutical products under contamination control protocols.

Leadership & Communication:

• Ability to guide and support junior team members during production activities.

• Strong interpersonal skills to collaborate cross-functionally and report issues effectively.

• Problem Solving & Improvement:

• Able to identify deviations, assist with root cause analysis, and support continuous improvement initiatives (e.g., 5S, Kaizen).

Adaptability & Reliability:

• Comfortable working in a fast-paced, 24/7 environment with rotating 12-hour shifts, overtime, weekends, and holidays.

• Committed to quality, safety, and meeting production goals.

• Physical & Safety Readiness:

• Able to lift/move up to 30 lbs, stand for extended periods, and work in cleanroom/cold conditions with required PPE.

• Must follow strict gowning and allergen safety protocols (e.g., cephalosporin sensitivity).

Important Considerations:

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:

• Perform a combination of sedentary work and extended walking/standing during 12-hour shifts.

• Lift, carry, push, or pull up to 30 lbs (with material handling assistance as needed).

• Perform repetitive motions (e.g., bending, squatting, reaching, twisting) throughout your shift.

• Work in cleanrooms, cold/wet areas, or other controlled environments requiring full gowning (no makeup, jewelry, nail polish, or artificial nails).

• Be exposed to moving machinery, confined spaces, and chemicals (e.g., alcohol, acids, buffers, Celite) that may require respiratory protection.

• Work across packaging, quality, and production rooms throughout the facility.

• Meet visual standards (20/20 near and distance vision, with or without correction) and must not be colorblind (if performing visual inspection).

• Be available to work 12-hour shifts on a 2-2-3 rotation, including weekends, holidays, overtime, and off-shift hours as required.

• Be able to meet any immunization requirements and work safely around potential allergens (e.g., cephalosporins, if applicable).

Shift Requirements and Associated Compensation:

Shift Schedule: 2-2-3 Rotation, 5:00 PM – 5:30 AM

Takeda Compensation and Benefits Summary

For Location:

USA - IL - Round Lake - Drug Delivery

U.S. Hourly Wage Range:

$18.85 - $29.62

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Locations

USA - IL - Round Lake - Drug Delivery

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

No