BioSpace
Manufacturing Technician III
– Takeda
Job Description About the Role: The Manufacturing Technician III reports to a Manufacturing Supervisor. In this role you will execute all processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply. You will participate in departmental projects and quality working teams as required. Under the general direction of the lead technician and the supervisor, you will oversee the hands‑on execution of all activities in the production area. In addition to making routine revisions to documents, you may rewrite complex procedures or initiate new procedures as applicable. You will have enough applied technical knowledge to perform complex troubleshooting tasks and may assist during new technology transfers into manufacturing. Technical and administrative competence to organize and lead production activities, including demonstrating leadership in cGMP compliance and environmental health and safety skills, is required. This position works 5:00 am – 5:30 pm on a rotating 2‑2‑3 schedule.
How You Will Contribute
Manage personal training plan to enhance knowledge, skills, and capabilities
Troubleshoot process & equipment problems in a timely manner to minimize manufacturing downtime
Conduct safety Gemba’s and provide coaching daily to ensure technicians adhere to proper ergonomic techniques
Support all local manufacturing operations
Operate general production equipment (e.g., filling, inspection, & packaging equipment)
Complete relevant paperwork following GDP/GMP guidelines
Manually clean all portable equipment and small parts
Participate on continuous improvement teams
Receive and distribute supplies into the production area
Ensure all components necessary for manufacturing are prepped and ready to meet schedule adherence, and set up next shift for success
Assemble and operate manufacturing equipment
Coordinate other groups such as maintenance / metrology to ensure preventative maintenance is performed
Demonstrate proficiency in electronic systems such as EBM, JDE, etc.
What You Bring To Takeda
High school diploma or GED with 4+ years of related work experience, or an AA degree or higher with 2+ years 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
Have a good understanding of cGMP regulations
Familiarity with pharmaceutical production equipment including autoclave, DP oven, and CIP/SIP
Proficient in different mathematical disciplines and able to work with both metric and U.S. measurement standards
Knowledge of basic chemical and biological safety procedures
Important Considerations
Work in a controlled environment requiring specialized gowning and protective clothing for head, face, hands, feet, and body, including additional hearing protection for loud areas
Must remove all makeup, jewelry, contact lenses, nail polish, and/or artificial fingernails while in the manufacturing environment
Work in a cold, wet environment
Work multiple shifts, including weekends, or be asked to work supplemental hours as necessary
Work around chemicals such as alcohol, acids, buffers, and Celite that may require respiratory protection
Must be able to work a 12‑hour shift (5:00 am – 5:30 pm or 5:00 pm – 5:30 am) in a 2‑2‑3 rotation
Requires flexibility to work during off‑shift hours and/or support other shifts as needed
Must be able to work overtime as required
Must be able to carry up to 30 lbs, lift up to 30 lbs, push/pull up to 30 lbs with material handling equipment assistance
Must stand and/or walk for an extended period over an 8–12 hour shift between rooms and across the site
Must walk within and between quality and packaging rooms, and throughout the entire plant
May require bending, twisting, reaching overhead, and/or squatting motions for certain tasks
Repetitive motions with hands, wrists, turning head, bending at knees and waist
20/20 vision, both near and distance, with or without glasses/contacts (Applies to roles performing visual inspection only)
Must not be colorblind (Applies to roles performing visual inspection only)
More About Us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best‑in‑class patient support programs. Takeda is a patient‑focused company that inspires and empowers you to grow through life‑changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Compensation and Benefits
U.S. Hourly Wage Range:
$20.53 – $32.26
Eligible for short‑term incentives and a 401(k) plan with company match
Medical, dental, vision insurance, short‑term and long‑term disability coverage, basic life insurance, tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits
Up to 80 hours of sick time per calendar year; new hires accrue up to 120 hours of paid vacation
Location USA – IL – Round Lake – Drug Delivery
Job Information Worker Type:
Employee
Worker Sub‑Type:
Regular
Time Type:
Full time
Job Exempt:
No
Seniority level:
Mid‑Senior level
Employment type:
Full‑time
Job function:
Management and Manufacturing
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.
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– Takeda
Job Description About the Role: The Manufacturing Technician III reports to a Manufacturing Supervisor. In this role you will execute all processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply. You will participate in departmental projects and quality working teams as required. Under the general direction of the lead technician and the supervisor, you will oversee the hands‑on execution of all activities in the production area. In addition to making routine revisions to documents, you may rewrite complex procedures or initiate new procedures as applicable. You will have enough applied technical knowledge to perform complex troubleshooting tasks and may assist during new technology transfers into manufacturing. Technical and administrative competence to organize and lead production activities, including demonstrating leadership in cGMP compliance and environmental health and safety skills, is required. This position works 5:00 am – 5:30 pm on a rotating 2‑2‑3 schedule.
How You Will Contribute
Manage personal training plan to enhance knowledge, skills, and capabilities
Troubleshoot process & equipment problems in a timely manner to minimize manufacturing downtime
Conduct safety Gemba’s and provide coaching daily to ensure technicians adhere to proper ergonomic techniques
Support all local manufacturing operations
Operate general production equipment (e.g., filling, inspection, & packaging equipment)
Complete relevant paperwork following GDP/GMP guidelines
Manually clean all portable equipment and small parts
Participate on continuous improvement teams
Receive and distribute supplies into the production area
Ensure all components necessary for manufacturing are prepped and ready to meet schedule adherence, and set up next shift for success
Assemble and operate manufacturing equipment
Coordinate other groups such as maintenance / metrology to ensure preventative maintenance is performed
Demonstrate proficiency in electronic systems such as EBM, JDE, etc.
What You Bring To Takeda
High school diploma or GED with 4+ years of related work experience, or an AA degree or higher with 2+ years 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
Have a good understanding of cGMP regulations
Familiarity with pharmaceutical production equipment including autoclave, DP oven, and CIP/SIP
Proficient in different mathematical disciplines and able to work with both metric and U.S. measurement standards
Knowledge of basic chemical and biological safety procedures
Important Considerations
Work in a controlled environment requiring specialized gowning and protective clothing for head, face, hands, feet, and body, including additional hearing protection for loud areas
Must remove all makeup, jewelry, contact lenses, nail polish, and/or artificial fingernails while in the manufacturing environment
Work in a cold, wet environment
Work multiple shifts, including weekends, or be asked to work supplemental hours as necessary
Work around chemicals such as alcohol, acids, buffers, and Celite that may require respiratory protection
Must be able to work a 12‑hour shift (5:00 am – 5:30 pm or 5:00 pm – 5:30 am) in a 2‑2‑3 rotation
Requires flexibility to work during off‑shift hours and/or support other shifts as needed
Must be able to work overtime as required
Must be able to carry up to 30 lbs, lift up to 30 lbs, push/pull up to 30 lbs with material handling equipment assistance
Must stand and/or walk for an extended period over an 8–12 hour shift between rooms and across the site
Must walk within and between quality and packaging rooms, and throughout the entire plant
May require bending, twisting, reaching overhead, and/or squatting motions for certain tasks
Repetitive motions with hands, wrists, turning head, bending at knees and waist
20/20 vision, both near and distance, with or without glasses/contacts (Applies to roles performing visual inspection only)
Must not be colorblind (Applies to roles performing visual inspection only)
More About Us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best‑in‑class patient support programs. Takeda is a patient‑focused company that inspires and empowers you to grow through life‑changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Compensation and Benefits
U.S. Hourly Wage Range:
$20.53 – $32.26
Eligible for short‑term incentives and a 401(k) plan with company match
Medical, dental, vision insurance, short‑term and long‑term disability coverage, basic life insurance, tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits
Up to 80 hours of sick time per calendar year; new hires accrue up to 120 hours of paid vacation
Location USA – IL – Round Lake – Drug Delivery
Job Information Worker Type:
Employee
Worker Sub‑Type:
Regular
Time Type:
Full time
Job Exempt:
No
Seniority level:
Mid‑Senior level
Employment type:
Full‑time
Job function:
Management and Manufacturing
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.
#J-18808-Ljbffr