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Manufacturing Technician II - Nights

Job in Round Lake, Lake County, Illinois, 60073, USA
Listing for: TAKEDA PHARMACEUTICALS AMERICA, INC.
Full Time position
Listed on 2026-01-01
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing Production
Job Description & How to Apply Below

Manufacturing Technician II - Nights role at TAKEDA PHARMACEUTICALS AMERICA, INC.

Job : R0164094 | Posted: 10/22/2025 |

Location:

Round Lake Beach, IL | Shift: 12‑hour 5:00pm – 5:30am

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
  • Understanding of cGMP regulations in a pharmaceutical manufacturing environment.
  • A self‑starter with a positive attitude and good time management skills.
  • Ability to remain professional at all times.
  • Meet the deadlines of individual production tasks during shift.
  • Follow the company’s safety and quality guidelines.
  • 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 following GDP/GMP guidelines.
  • Perform daily cleaning of the production area to maintain in GMP fashion.
  • Train our employees/contractors on procedures.
  • Communicate issues related to safety, quality, compliance and equipment to the manufacturing lead operator and supervisor.
Qualifications
  • High school diploma or GED.
  • 2+ years of experience or AA or higher and 1+ years of related work experience.
  • Must be able to speak, read, write, and follow detailed written and oral instructions in English.
  • Good interpersonal skills and ability to work effectively and efficiently in a team environment.
  • Understanding of cGMP regulations in a pharmaceutical manufacturing environment.
Legal Notice

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.

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