107 Manufacturing jobs in Gurnee

Location: Des Plaines, IL, 60018

Duration: 12 Months

Shift: 6:00 AM to 2:30 PM

Job Description: This position is Non Exempt. Hours over 40 will be paid at time and a half. Responsible for proper maintenance and operation of drug manufacturing equipment. Accurately weighing raw materials and active ingredients and combining them into.

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

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

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 will inspire and empower 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, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

#GMSGQ #ZR1 #LI-MA1

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

USA - IL - Round Lake - Drug Delivery

U.S. Hourly Wage Range:

$18.85 - $29.62

The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job?The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location.

U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

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

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

About the Role:

The Lead Manufacturing Technician is responsible for executing 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 both departmental projects and any quality working teams which may be applicable. Under the general direction of the supervisor, this position shall oversee the hands-on execution of all activities in the production area. In addition to making routine revisions to documents, you will rewrite complex procedures or initiate new procedures as applicable. You will have enough applied technical knowledge to perform complex trouble shooting tasks and may even assist during the transfer of new technologies into manufacturing. The position requires technical and administrative competence to organize and lead production activities, including demonstrating leadership in cGMP compliance, and environmental health and safety skills.

How you will Contribute:

• Lead training efforts and mentoring for manufacturing tech progression from level 1-3

• Conduct safety Gemba's and provide coaching daily to ensure technicians are observing proper ergonomic techniques.

• Support all local manufacturing operations.

• Demonstrate proficiency in electronic systems such as (EBM, JDE, etc.)

• Operate general production equipment (such as Filling, Inspection, & Packaging equipment)

• Ensure 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.

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

• Assemble and operate filtration systems.

• Ensure all components necessary for Manufacturing are prepped and ready to meet schedule adherence in addition to setting up incoming shift for success.

• Troubleshoot process & equipment problems promptly to minimize Manufacturing downtime.

• Coordinate with other groups such as maintenance/metrology to ensure preventative maintenance is done per plan.

• May perform other duties as assigned.

What you bring to Takeda:

• High school diploma or GED. 6+ years of experience or AA or higher with 4+ years related work experience

• Will speak, read, write, and follow detailed written and oral instructions in English.

• Must have excellent written and verbal communication skills and understanding of cGMP regulations.

• Procedural writing skills, required.

• Experienced with pharmaceutical production equipment including autoclave.

• Must be able to apply quantitative analysis to analyze process performance.

• Incumbent must be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurement.

• Highly effective interpersonal skills and be able to work in a team environment.

• Knowledgeable of chemical and biological safety procedures.

• Good computer skills

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. You may:

• Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.

• Need to remove all make-up, 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.

• Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.

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 will inspire and empower 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, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

#GMSGQ #ZR1 #LI-MA1

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. 

For Location:

U.S. Hourly Wage Range:

The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. 

U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. 

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.

Job Exempt

Job Description

Job Title: Drug Manufacturing Technician

Requisition ID: ABOJP00041081

Location: Des Plaines, IL

Contract Duration: 07/07/2025 – 07/07/2026

Work Schedule: Monday–Friday, 6:00 AM – 2:30 PM

Hours per Week: 40

Pay Rate: $22.00/hr

Benefits: Medical, Vision, Health Care, 25K Life Insurance

Job Description:

This is a Non-Exempt position. Hours worked over 40 per week will be paid at time and a half.

The Drug Manufacturing Technician is responsible for the proper maintenance and operation of drug manufacturing equipment in a cGMP environment. Key tasks include accurately weighing and blending raw materials and active ingredients, maintaining a clean and orderly work area, and ensuring all operations are documented per cGMP standards.

Key Responsibilities:

• Operate drug manufacturing equipment effectively and safely.
• Accurately weigh raw materials and active ingredients.
• Blend materials according to formula and procedures.
• Maintain equipment and facility in a clean, good repair state.
• Complete work orders and batch records with minimal errors.
• Follow all procedures exactly, maintaining strict adherence to cGMP standards.
• Complete required training in a timely manner, including safety and cGMP.
• Capable of working independently or within a team.

Qualifications:

• Education: High School Diploma or GED equivalent required
• Experience: Entry-level role – prior experience is helpful but not mandatory

WIELAND JOB FAIR

WALK-INS WELCOME | ON THE SPOT OFFERS!

THURSDAY, JULY 31ST, 2025

12PM - 7PM CST

LOCATION: 340 EAST IL ROUTE 22, LAKE ZURICH, IL

Wieland - Creating Value for Generations!

Wieland is a global leader in copper and copper alloy manufacturing, processing, and distribution. We provide a large product and service portfolio including power, automotive, ammunition, coinage, construction materials, refrigeration, electronics and many other industries. To us, metal is more than material.

Wieland's Cultural Values

Wieland's culture is what makes for a fun and rewarding place to work! As a company, we benefit daily from our employees' knowledge and abilities. With our cultural vision, we place our core values at the heart of everything we do: safety , ambition , optimism , reliability , ownership , diversity , & respect .

Wieland is hiring a Manufacturing Cost Estimator . The Manufacturing Cost Estimator will be responsible for performing functions to determine accurate cost of producing manufactured product; including determining proper material, outside operations, labor and machine to be utilized in production process for each part quoted. Work across other departments to derive information needed. Perform analysis on large vendor pricing for obtaining the best possible cost of each material and/or service purchased. This role is located in Lake Zurich, IL and will be fully onsite.

Base Salary Range: $56,000 - $79,000

May be eligible for a variable compensation plan bonus based upon company performance within fiscal year cycle.

At Wieland, we recognize that attracting the best talent is key to our strategy and success as a company. As a result, our ranges reflect our good faith estimate to pay fairly. The final pay offered to a successful candidate will be based upon various factors unique to each individual that may include but are not limited to years of eperience, industry knowledge, technical skills, education, qualifications, etc.

Manufacturing Cost Estimator Responsibilities:

Provide timely manufacturing product quotes based on customer requirements to existing & potential customer base.
• Develops and maintain performance metrics for quoting team (i.e. completion to target, Com. Ex.).
• Source material and outside operations requests with vendors.
• Conduct Contract Review as to verify that all correct information is included in system prior to initiation of production and costs updated.
• Assist outside & inside sales representatives to service potential and existing customers as requested.
• Identify additional supplier options able to provide competitive quality products on time.
• Identify secondary sources of supply, when applicable.
• Investigate and research new materials, suppliers and processes to achieve the best possible quality, reliability, prices, continuity and delivery and achieve operational excellence
• Keep abreast of materials and material pricing trends that effect company products. Share this with our management team, as appropriate.
• Participate in APQP meetings and process to ensure new products costs within budget.
• Maintains standard metals pricing and stocking lists from metals suppliers.
• Lead project teams to accomplish MBP's goals, as related to our Annual Strategic Goals and our Balanced Scorecard initiatives.
• Maintains knowledge of processing rates and methods from operations to accurately quote.

Manufacturing Cost Estimator Qualifications:

• Ability to create written and verbal instructions
• Excellent written and verbal communication
• Strong computer skills (Outlook, Word, Excel, Powerpoint, Access)
• Strong mathematical and analytical skills
• Advanced blueprint reading
• Knowledge of ferrous and/or non-ferrous materials
• Knowledgeable in heat treating and metals processing
• Strong mechanical aptitude
• Background in CNC turning and milling
• Knowledge of aerospace flow down requirements
  
  COURSEWORK OR EQUIVALENT EXPERIENCE
• High school diploma or GED required, Bachelor's preferred
• 5 years manufacturing experience in a CNC turning job shop required
• Knowledge of Aerospace product processing and approved sources
• Previous quoting experience with Aerospace OEM products (Raytheon, Bell, HDI, Collins)
• Experience with copper-based alloys preferred
• Previous experience completing CNC set-ups and operations preferable
• Minimum 5 years of experience in cost calculating for manufactured products
• Strong math skills and attention to detail, accuracy is a must

Joining Wieland's team gives you.

• Benefits - Starting on Day 1! Including Medical, Dental, Vision, Disability, Life & more!
• Retirement Savings - 401(k) contribution + match.
• Work/Life Balance - Paid Vacation & Holidays.
• Growth Opportunities - We have over 9,000+ employees worldwide and 40+ locations in North America alone. Growth opportunities are limitless!
• Wellness Programs - Wieland encourages participation in our unique and personalized approach to wellness, where you are eligible to earn healthcare premium discounts as well as HSA employer contributions based on your status within the program.
• Sustainability - Wieland continues to break ground with eco-friendly solutions and push the barrier in sustainability for future generations.

Wieland is an equal opportunity and affirmative action employer . We celebrate diversity and are committed to fostering an inclusive environment for all employees. Come join Wieland today and help us continue to build a global corporation we are all proud to belong to.

100% onsite

The primary focus of the Manufacturing Technician role will be the cleaning and sanitization of the Libertyville Manufacturing Facility, Warehouse, and any other areas or satellite facilities designated by management. The MFG Technician will be part of a select team to perform these cleanings on a daily rotational basis according to Current Good Manufacturing Practices (cGMP's), relevant Standard Operating Procedures (SOPs) and facility scheduling. The Technician will also be responsible for proper GDP documentation of these cleanings, and responsible for completing all trainings necessary to remain in compliance with company policies and SOPs.

DUTIES AND RESPONSIBILITIES:
• The MFG Technician will be a professional individual with a strong work ethic, be highly dependable, and able to adhere to their assigned work schedule.
• They will be responsible as a part of a select team to perform the daily cleaning and sanitization of facilities and equipment according to SOPs.
• Assist in staging of materials for MFG processes
• Perform proper cleaning techniques per SOP such as vacuuming, trash disposal, wiping of equipment, and mopping of walls, ceilings and floors.
• Responsible for the operation and maintenance of all cleaning equipment.
• Responsible for the preparation of cleaning/sanitization solutions and cleaning materials to specifications outlined in SOPs.
• Accurately documents solution preparation and cleaning activities in logbooks in accordance to Good Documentation Practices (GDPs), and company SOPs.
• Must possess the willingness to learn new concepts in order to fully understand aseptic technique and demonstrate proper cleanroom behavior at all times.
• Works on routine manufacturing cleaning and sanitization assignments per written procedures, where ability to recognize deviation from accepted practice is required.
• Adheres to Good Manufacturing Practices and standard operating procedures.
• Completes work instructions and maintains clean room environment to comply with regulatory requirements.
• Trains for proficiency in process systems (i.e. Oracle interfaces) and some supporting business systems.
• Assists in maintaining material and components inventory level.
• Supports safe work environment.
• Receives, trains on, and understands general instructions for routine work.
• Work in teams and have continual interaction with members of his/her team as well as other manufacturing teams throughout the production process in order to exchange information regarding the batch(s) in process.

Education:
High school diploma/GED required

• Operate conventional and CNC machine shop equipment (e.g., lathes, mills, grinders, saws) to produce precision parts.
• Perform machine set-ups and adjustments based on blueprints and engineering specifications.
• Inspect finished parts to ensure they meet required tolerances.
• Program, grind, inspect, and document work as required.

• High school diploma or equivalent; technical training a plus.
• Basic understanding of machining processes and mechanical drawings.
• Willingness to learn and follow instructions in a hands-on environment.
• Comfortable working the night shift (2:00 pm - 10:30 pm) and with pay ($18 an hour)
• Strong attention to detail and commitment to safety and quality.

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