103 Manufacturing jobs in Grayslake

Manufacturing Engineer

New
60714 Niles, Illinois LSL Healthcare

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Job Description

LSL Healthcare is a leading national supplier and a certified Minority Business Enterprise (MBE), recognized as a trusted partner in healthcare supply chains. We specialize in customizing medical and surgical kits, procedure trays, and disposable medical equipment. Committed to quality, value, and exceptional customer service, we provide tailored solutions to meet the unique needs of healthcare facilities nationwide.


Role Description

We are seeing a proactive and technically skilled Manufacturing Engineer to support and improve manufacturing processes for medical devices. This role will lead efforts in design transfer, process validation, automation deployment, and cost-effective scaling of manufacturing capabilities. This role will also contribute to project planning, budget management, and compliance activities working closely with cross-functional teams, and suppliers to ensure product quality, operational readiness, and distributor fulfillment


Key Responsibilities

  • Develop, validate, and optimize manufacturing processes to ensure quality, repeatability, and scalability.
  • Lead process improvement projects for assembly, packaging and labeling, tailored to distributor requirements.
  • Support the design, development and implementation of automated and semi-automated equipment for manufacturing processes.
  • Oversee and support IQ/OQ/PQ validations conducted
  • Collaborate with quality control teams to ensure adherence to quality standards and regulatory requirements
  • Drive continuous improvement initiatives through Lean and Kaizen methodologies.
  • Partner with Quality and Regulatory to ensure consistent operational excellence across external partners.
  • Ensure that manufacturing processes (including packaging and labeling) are suitable for distribution
  • Plan, coordinate, and execute manufacturing projects, ensuring timely completion within budgetary constraints
  • Develops and supports Standard Operating Procedures/Work Instructions with internal requirements to ensure regulatory and quality compliance.
  • Partner with supply chain and finance to track cost saving initiatives, cost- of poor quality, or cost per unit improvements.
  • Develop and maintain project plans, schedules and trackers for design transfer, process validation, and automation projects.
  • Participate in supplier audits and support CAPA investigations related to outsourced production.
  • Ensure manufacturing documentation aligns with FDA (21 CFR Part 13485, and company QMS requirements.


Qualifications

  • Proficiency with Microsoft office suite (PowerPoint, Excel, Word, etc.) and Windows
  • Analytical mindset with the ability to use data and information to drive decisions
  • The ability to communicate internally to all levels of the organization and externally with suppliers
  • Candidates are preferred that have experience managing medium sized projects as a Project Manager in Manufacturing (Medical or Non-Medical, but Medical is preferred).
  • Strong knowledge of FDA (21 CFR Part 820) ISO 13485, GMP and QMS documentation standards)


Skills & Experience

  • Bachelor’s degree in Engineering, Business Administration, Supply Chain, Logistics or related field, or an equivalent level of experience
  • 5-7 years of experience in manufacturing or relevant experience
  • Demonstrated ability to apply Lean, Kaizen, or Six Sigma methodologies (Certification preferred)
  • Bilingual in Spanish and English is a plus


Compensation & Benefits:

The anticipated salary range for this position is $90,000 - $120,000 annually. The actual pay rate will vary based on applicant’s location, education, relevant experience, skills, and education. This role is eligible for bonus and/or performance-based incentives.


LSL Healthcare offers a competitive salary, performance-based incentives, and a comprehensive benefits package, including health insurance, dental, vision, life, short- term and long-term disability, AD&D insurance, and 401(k) savings plan with employer match, paid time off and holiday pay, as well as professional development opportunities.


LSL Healthcare is an equal opportunity employer and prohibits discrimination and harassment of any kind. All applicants will be considered for employment without regards to race, color, religion, age, sex, sexual orientation, gender identity, national origin, veteran or disability status, or any other status protected by law. LSL is committed to cultivating a culture of diversity and inclusion promoting teamwork.

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Manufacturing Engineer

60047 Lake Zurich, Illinois LHH

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Job Description

LHH Recruitment Solutions has partnered with a growing organization, and they are seeking a motivated Manufacturing Engineer to join their team. This is more than just a job — it's a chance to be part of a company with over four decades of success and a reputation for excellence. You’ll work on high-impact projects from concept through production, contributing to automation, product development, and continuous improvement initiatives.


Key Responsibilities:

  • Lead engineering support to reduce scrap, optimize material usage, and minimize downtime.
  • Manage factory automation projects and process/equipment changes.
  • Maintain product drawings and documentation; drive standardization and control.
  • Champion continuous improvement in layouts, methods, and material flow.
  • Collaborate with cross-functional teams on new product development.
  • Assist in packaging design and ensure quality control systems are in place.
  • Conduct capacity analysis and recommend equipment upgrades.
  • Evaluate and improve operational efficiency.


Qualifications and Skills:

  • Bachelor’s degree in Mechanical or Industrial Engineering.
  • Minimum 3 years of experience in a manufacturing engineering role.
  • Proficiency in AutoCAD; SolidWorks preferred.
  • Strong problem-solving and communication skills.
  • Comfortable with hands-on work in a production environment.
  • Skilled in Microsoft Office (Word, Excel, PowerPoint).
  • Experience with prototyping, testing, and reporting is a plus.


Compensation Range: $80,000-$110,000


Benefits Offered: 10 days of vacation, paid sick leave where applicable by state law, Medical Insurance, Dental Insurance, Vision Insurance, 401K, and Life Insurance.


If you are a passionate Manufacturing Engineer looking for a new and rewarding career, please apply today! You don’t want to miss out on this opportunity!


LHH is a leader in permanent recruitment—and in the placement of top talent. Our areas of specialty include office administration, customer service, human resources, engineering, and supply chain and logistics. Please feel to check us out and apply for other opportunities if this role isn’t a perfect match.


Equal Opportunity Employer/Veterans/Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit

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MANUFACTURING TECH

60047 Lake Zurich, Illinois LISI

Posted 4 days ago

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Job Description

Termax is a dynamic manufacturing and engineering company specializing in metal, plastic and rubber fastening systems. Our 250,000 square foot facility in Lake Zurich, IL, provides manufacturing, engineering and in-house tooling capabilities that world-class organizations rely on to support their operations.

Job Description Summary

As a member of the automation team this individual will assist in the design, implementation, and maintenance of assembly equipment to assist our fastener assembly group.

Duties and Responsibilities

  • Assist in the build and de-bug of assembly machinery and systems.
  • Able to align and setup vision inspection system.
  • Able to debug and setup PLC's, HMIs, and servos.
  • Repair electrical, mechanical, and pneumatic machine components.
  • Read and understand assembly and detail blueprints to build and modify machines.
  • Create minor components such as brackets and spacers from detail drawings.
  • Set pneumatic cylinder sensors for proper functionality.
  • Adjust cylinder travel when required to align machine motions.
  • Align and set sensors for proper function.
  • Maintain the department/ work area clean and organized.
  • Follow ISO/IATF, safety, and environmental procedures as well as department and corporate policies and procedures.
Authority
  • Authority to stop machine operation when quality or safety issues are observed or reported.
Job Knowledge; Skills and Abilities
  • Basic knowledge in the design and troubleshooting of complex machine controls systems and programs.
  • Basic knowledge in PLC programming.
  • Basic knowledge on feeding and sorting bowls.
  • Know how to safely use power equipment.
  • Understand function of pneumatic valves and how to plumb tubing and adjust air flow settings.
  • Understand relationship of all machine sensors regarding the function of the machine.
  • Understand all assembly machine functions regarding debugging machine issues.
  • Understanding of machine and operator safety concerns in a production environment.
  • Basic understanding of vision sensors and systems helpful but not required.
  • Basic knowledge of electrical wiring and diagrams.
  • Basic understanding of robot controls and mechanical components.
  • Knowledge of measuring equipment (tape measure, calipers).
  • Ability to understand machine based mechanical, pneumatic, and electrical issues and correct them.
  • Ability to use basic hand tools and safely use drill press and band saws.
  • Able to complete work orders.
  • Must be able to lift up to 50 lbs.
Education and Training
  • Minimum High School Diploma or equivalent.
  • Training in mechanics and electronics helpful but not required.
  • Forklift operational training helpful but not required.
Tools and Equipment
  • Power and basic hand tools including wrenches and screw drivers.
  • Understanding of electronic measuring devises (voltmeter, comparator) desired but not necessary.
  • Steel toed shoes, safety glasses and ear plugs are required at all times.


The duties listed above are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related or a logical assignment to the position.

The job description does not constitute an employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change.

Termax is an equal opportunity at will employer and does not discriminate against any employee or applicant for employment because of age, race, religion, color, disability, sex, gender, sexual orientation or national origin.

Competitive Benefits Include: Medical, Dental, Vision, Health Savings Account (HSA), Flexible Savings Account (FSA), Life Insurance, Paid Time Off and 401K (Roth and Traditional). Tuition reimbursement to support your development.

We maintain a drug-free workplace and perform pre-employment substance abuse testing.

E-Verification: In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Come join the greatest team on the planet!

No recruiters, please.
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Manufacturing Technician

60089 Buffalo Grove, Illinois Volt

Posted 4 days ago

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Job Description

Let Volt help move you forward

Volt is immediately hiring for a Manufacturing Technician in Buffalo Grove, IL.

We are looking to find someone with machine shop skills that wants to learn surface grindig and Dead true grinding.

As a Manufacturing Technician you will:

  • Works with engineers in set-up and calibration tasks.
  • Works with engineers in conducting experiments.
  • Performs rework and quality testing related to the production of parts, components, subassemblies and final assemblies.
  • Uses sophisticated programs to collect and evaluate operating data to conduct on-line adjustments to products, instruments or equipment.
  • Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
This is a full-time opportunity.

The ideal candidate will have:
  • Machine Shop Skills are a plus
  • Prior assembly line experience preferred.
  • Ability to read blue print and schematics.
  • Ability to write routine reports and correspondence.
  • Able to read and comprehend moderately complex instructions.
  • Ability to effectively present information in small group situations.
  • Candidates selected must meet all pre-screening eligibility requirements

Pay Rate: $21.00 - $22.00 per hour (Monday - Friday7am-330pm)

*Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc.

Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible.

Benefits: Volt offers benefits (based on eligibility) that include the following: health, dental, vision, term life, short term disability, AD&D, 401(k), Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP).

Volt is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Volt is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please email or call . Please indicate the specifics of the assistance needed.

Volt does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

Volt is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Volt is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please click here or call . Please indicate the specifics of the assistance needed.
Volt does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.
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Manufacturing Scheduler

60073 Round Lake Beach, Illinois Takeda Pharmaceutical Company Ltd

Posted 10 days ago

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Job Description

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:

You are a member of the production scheduler team within the Round Lake site. As the Manufacturing Scheduler, they will create and update production schedules for the Filling, Inspection, and Packaging areas. The Manufacturing Scheduler will ensure the accuracy of the schedule and identify opportunities to minimize delays and to improve manufacturing processes. You will work together with manufacturing team members and support group members. Also, the manufacturing scheduler will build and improve systems to enhance schedule management, communication, and adherence.

How you will Contribute:
  • Maintain, and manage the daily manufacturing production schedules (Filling, Inspection, and Packaging). Lead daily scheduling meetings.
  • Oversee production scheduling changes directly to shop floor leadership.
  • Create advanced, weekly production schedules for all manufacturing departments.
  • Schedule non-production related activities such as qualifications, PM, corrective maintenance, engineering and validation projects.
  • Interface with Manufacturing, Supply Chain/Warehousing, Validation, Maintenance, Engineering, QA, and QC to forecast weekly production.
  • Create mock schedules based on alternate production conditions/scenarios for management.
  • Identify improvement opportunities in the schedule or in the process as related to WIP management.
  • Anticipate potential issues and conflicts and present options for resolution to functional management to optimize processes and minimize delays in the production.
  • Interface with production scheduling tools (Excel and/or INFOR), EBM, JDE, and other supporting tools.
  • Collect data and perform data analysis related to WIP, cycle time, lead time, etc.
  • Establish and maintain schedule adherence measures to drive improvement.
  • Manage the JD Edwards Work Order process (opening, closing, lot number assignment, etc.).
  • Participate in continuous improvement related activities in the site.
  • Perform other support activities for production needs as necessary.
What you bring to Takeda:
  • High School Diploma or GED plus 5+ years of related experience OR bachelor's degree in science, engineering or other related technical field and 2+ years of related experience.
  • General knowledge of biopharmaceutical manufacturing processes and unit operations preferred.
  • Math and computer skills (Microsoft Office programs such as PowerPoint, Excel, Word).
  • Experience in INFOR, EBM, scheduling software, or similar systems.
  • Must be able to read and follow detailed written instructions.
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:

  • 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, as necessary.
  • 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-Onsite

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. Base Salary Range:

$70,000.00 - $110,000.00

The estimated salary range reflects an anticipated range for this position. The actual base salary 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 base salary 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 and/ or long-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

Yes
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Manufacturing Supervisor

60089 Buffalo Grove, Illinois Siemens

Posted 1 day ago

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Job Description

**Job Family:** Buildings
**Req ID:**
Here at Siemens, we take pride in enabling sustainable progress through technology. We do this through empowering customers by combining the real and digital worlds. Improving how we live, work, and move today and for the next generation! We know that the only way a business thrives is if our people are thriving. That's why we always put our people first. Our global, diverse team would be happy to support you and challenge you to grow in new ways. Who knows where our shared journey will take you? 
Our Smart Buildings help to create efficient, safe, adaptable, and responsible environments. Our aim isn't just about improving buildings; it's about creating perfect places that improve people's lives. 
**Transform the everyday with us!**
**We are looking for a 2nd Shift Production Supervisor. This position will be based at for our Buffalo Groove, IL factory.**
The Manufacturing Supervisor is the key driver of all daily production related processes and the hub of information transfer between the hourly assembly workforce and Management, Engineering, Quality Control, Purchasing and Planning. The base shift is 3PM-11PM, This person will have 20-30 direct reports.
**As a Manufacturing Supervisor, you will:**
+ Improve safety for all personnel that work in and around production lines
+ Drive initiatives to reduce production errors, improve quality and increase productivity
+ Adhere to production schedule, assigning personnel to work areas, monitoring
+ progress, resolving line constraint problems, and reporting results through shift production summaries
+ Plan, oversee and document training of personnel
+ Conduct annual employee performance reviews
+ Work closely with purchasing, planning and warehouse teams to ensure material availability and schedule adherence
+ Liaison between Manufacturing and Engineering
+ Support performance measurement and documentation of manufacturing processes
+ Drive continuous improvement projects
+ Support digitalization efforts to implement tools such as Digital Work Instructions, Operator Displays, Performance/Status Dashboards, and other connected tools
**You'll make an impact with these qualifications:**
Basic Qualifications:
+ 2+ years of successful experience in an Assembly/Manufacturing or related field in a supervisor role.
+ Mechanical Aptitude with experience using hand tools
+ Bachelor's degree (Engineering preferred) or equivalent experience
+ Project Management Experience
+ Proficiency in data collection and analysis.
+ Able to interpret or learn to interpret engineering drawings and schematics.
+ Strong leadership and time management experience.
+ Demonstrates full understanding and application of management approaches for work direction, motivation, talent development and performance management.
+ Experience collaborating and team building with different internal organizations and locations.
+ Legally authorized to work in the United States on a continual and permanent basis without company sponsorship
Preferred Qualifications:
+ Experience with Microsoft Office Products.
+ Experience with SAP or similar MRP system.
**Ready to create your own journey?**  Join us today. 
**About Siemens:**   
We are a global technology company focused on industry, infrastructure, transport, and healthcare. From more resource-efficient factories, resilient supply chains, and smarter buildings and grids, to sustainable transportation as well as advanced healthcare, we create technology with purpose adding real value for customers.   
**Our Commitment to Equity and Inclusion in our Diverse Global Workforce**  
We value your unique identity and perspective. We are fully committed to providing equitable opportunities and building a workplace that reflects the diversity of society, while ensuring that we attract the best talent based on qualifications, skills, and experiences. We welcome you to bring your authentic self and transform the everyday with us.
#SiemensMFGcareer #MFGBuffaloGrove #LI-SK1
66,220 113,520
**Organization:** Smart Infrastructure
**Job Type:** Full-time
**Category:** Manufacturing
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Manufacturing Engineer

60172 Roselle, Illinois ITW

Posted 1 day ago

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Job Description

**Job Description:**
The main responsibility of this position will be to drive continuous improvement in the areas of safety, quality, productivity, and cost reduction. This is a hands-on role that will support the manufacturing processes by driving the attainment of goals and KPI's through working with Plant Leadership. Needs to be self-motivated, energetic leader who will recognize areas needing improvement, implement effective solutions, and provide training to guide positive changes in plant processes and procedures leveraging the ITW Toolbox.
**Primary Responsibilities:**
+ Develop, test, and implement process adjustments and/or new manufacturing techniques to reduce manufacturing costs and waste, and to improve safety, product quality, manufacturing efficiency, and machine reliability.
+ Lead change through facilitating USa Events, writing standard operating procedures, and training key production employees on new work procedures and processes.
+ Utilizing ITW Toolbox training, identify and lead changes using 80/20, Inlining, USa, Product Line Simplification, and Market Rate of Demand tools as appropriate.
+ Provide key troubleshooting on dies, tooling, and machine parts to improve production processes.
+ Train and monitor operators on proper die setup/changeover techniques.
+ Design new parts to improve machine performance.
+ Understand machine capabilities for new product development and continuous improvement throughout the manufacturing processes.
+ Revise and develop prints for current tooling and production part using CAD/Solidworks.
+ Draft and design layout of equipment, materials, and workspace to achieve maximum efficiency.
+ Perform capacity planning and provide solutions to meet continued growth. Manage capital projects from quoting/approval stage through training & implementation.
+ Support maintenance in root cause analysis, strategies to reduce mechanical downtime, and drafting and implementing preventive maintenance practices.
+ Mentor and support the professional growth of fellow engineers and cross-functional team members by sharing technical expertise, promoting best practices, and fostering a culture of continuous improvement across operations.
+ Creating and maintaining business relationships with suppliers, vendors and contractors.
+ Perform other tasks and functions as directed for the benefit of the business.
**Job Requirements:**
+ Bachelor's degree in Engineering Required; Mechanical, Manufacturing or Industrial Engineering preferred
+ 2-5 years of experience in high-volume manufacturing environment
+ Knowledge and application of design, engineering and technology, computers and electronics, technology design, and problem solving
+ Proficiency in AutoCAD and /or SolidWorks CAD software
+ Experience with Value Stream Mapping, Six Sigma Tools, Lean Manufacturing, Automation, and Capital Project
+ Safety focused mindset able to identify unsafe actions/conditions
+ High level of written and oral communication skills, organizational planning, teamwork, analytical reasoning, and adaptability
+ Must be well organized, detailed oriented, and able to coordinate multiple projects simultaneously
+ Ability to work with hands and to work in mechanically oriented situations
+ Self-starter with a lot of energy to see projects through to completion
+ Proficiency in Microsoft Office and data analysis
**CRITICAL COMPETENCIES FOR SUCCESS**
+ Delivers results: Exhibit exceptional business acumen and excellent management skills to hold themselves accountable for consistently meeting ITW's targets.
+ Good Judgment: Ability to use good judgment and discretion. Must be adept at analysing facts and issues, identifying options, and able to decide and recommend a course of action.
+ Impeccable Integrity: Embodies and practices unquestioned personal and business integrity. Recognized as a highly credible business leader. Creates an environment of trust by acting with fairness and consistency, keeping commitments, and providing rationale for decisions.
+ Approachable: Inspires trust and confidence. Independent and organized work style.
+ Team Player: An aggressive, results-oriented individual who, at the same time, is the consummate team player. Respected by senior management, peers, and subordinates, and secure in technical abilities. In addition, able to command loyalty and a sense of commitment from all colleagues. Lives the ITW Values and promotes ITW culture.
+ Relationships Builder: Excellent relationship builder, understanding the internal and external customers' requirements.
+ Structure: Comfortable with ambiguity, change and ability to succeed within a matrix organizational structure.
**PHYSICAL DEMANDS:** The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to stand; walk; kneel; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is required to climb or balance. The employee must regularly lift and/or move up to 25 pounds, frequently lift and/or move up to 50 pounds, and occasionally lift and/or move up to 60 pounds.
**WORK ENVIRONMENT:** Th **e** work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Good working conditions involving occasional exposure to noise and chemicals, but with none present to the extent of being disagreeable.
**Compensation Information:**
Pay Range : $73,000 to $90,000
Our employees enjoy competitive, merit-based salaries, plus excellent Benefits including:
Health, Vision and dental insurance
Company Paid Life insurance/Short- and Long-term disability
401k Plan with generous company match
3 weeks' vacation, sick days, and holidays
Continuing education reimbursement program
Flexible spending accounts
_ITW is an equal opportunity employer. We value our colleagues' unique perspectives, experiences and ideas and create workplaces where everyone can develop their careers and perform to their full potential._
_As an equal employment opportunity employer, ITW is committed to equal employment opportunity and fair treatment for employees, beginning with the hiring process and continuing through all aspects of the employment relationship._
_All qualified applicants will receive consideration for employment without regard to race, color, sex, gender identity, sexual orientation, religion, national origin, age, disability, protected Veteran status or any other characteristic protected by applicable federal, state, or local laws._
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Manufacturing Supervisor

53158 Pleasant Prairie, Wisconsin Lilly

Posted 15 days ago

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Job Description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
**Job Description Supervisor PFS11**
Organization Overview:
The Filling Operations Teams are an essential part of Lilly's Kenosha County (LKC) Parenteral Manufacturing site. We manufacture and fill injectable parenteral products in state-of-the-art facilities to supply patients around the world. This position will work in a new facility with best in class, globally replicated production equipment. Operations team members will work with the latest industry technologies, while learning from global teams, to manufacture key current parenteral products and preparing for upcoming products.
This role will be responsible for direct line supervision of operators, providing administrative leadership to filling operations team members, and developing technical expertise of employees. The leader will also assure quality behavior in the area and suggest technical improvements for delivery and operation of the areas. This specific role will support PFS11, delivering new pre-filled syringe filling capacity to IPM.
**Responsibilities:**
+ Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
+ Ensure strict compliance with established policies/procedures (Safety, Production Procedures, Sanitization, Gowning, Etc.), ensure operators are trained appropriately.
+ Take ownership for implementation of countermeasures associated with audits, observations, inspection findings, and deviations.
+ Participate in planning of equipment prep, formulation and filling operations. Network with various areas to verify components and equipment are available for orders.
+ Identify/escalate issues to the Manager / Associate Director (if applicable).
+ Responsible for the coaching, development and performance evaluation of Operations personnel.
+ Act as both administrator and technical leader for operations, setting a good example through demonstrated knowledge of procedures, compliance with quality systems and use of proper technique.
+ Responsible for shop floor execution as it relates to business plan, GMP conformance, and OSSCE.
+ Ensure adherence to use of proper technique in isolator and Grade C operational areas.
**Basic Requirements:**
+ High School Diploma/GED
+ Completion of Post Offer Exam, Completion of Work Simulation or Completion of Administrative Skills Testing if applicable.
+ Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
**Basic Preferences:**
+ Ability to work cross-functionally with other areas of LKC Parenteral Manufacturing (Operations, Engineering, Maintenance, Quality, etc.)
+ Good interpersonal and communications skills to be able to work effectively in a team-based environment.
+ Previous parenteral manufacturing experience.
+ Strong understanding of quality systems in a manufacturing environment.
+ Flexible to work overtime, weekends, off-shifts.
+ Must be able to work a 3-2-2-3 shift schedule.
**Additional Skills/Preferences:**
+ Flexibility to support capital projects
+ Root Cause Analysis
+ Computer Proficiency
+ Leadership skills
+ Innovation and creativity
+ Teamwork/Interpersonal skills
+ Organizational skills
+ Attention to detail
**Additional Information:**
+ This role will be a 12-hour shift production schedule (3-2-2-3), 6am-6pm concurrent with scaleup and transition to production operations.
+ Project related travel may be required.
+ Applicant will work in various areas within LKC Parenteral where allergens may be present. Mobility requirements and exposure to allergens should be considered when applying for this position.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$35.33 - $51.83
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
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Manufacturing Engineer

Niles, Illinois LSL Healthcare

Posted today

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Job Description

LSL Healthcare is a leading national supplier and a certified Minority Business Enterprise (MBE), recognized as a trusted partner in healthcare supply chains. We specialize in customizing medical and surgical kits, procedure trays, and disposable medical equipment. Committed to quality, value, and exceptional customer service, we provide tailored solutions to meet the unique needs of healthcare facilities nationwide.

Role Description

We are seeing a proactive and technically skilled Manufacturing Engineer to support and improve manufacturing processes for medical devices. This role will lead efforts in design transfer, process validation, automation deployment, and cost-effective scaling of manufacturing capabilities. This role will also contribute to project planning, budget management, and compliance activities working closely with cross-functional teams, and suppliers to ensure product quality, operational readiness, and distributor fulfillment

Key Responsibilities

  • Develop, validate, and optimize manufacturing processes to ensure quality, repeatability, and scalability.
  • Lead process improvement projects for assembly, packaging and labeling, tailored to distributor requirements.
  • Support the design, development and implementation of automated and semi-automated equipment for manufacturing processes.
  • Oversee and support IQ/OQ/PQ validations conducted
  • Collaborate with quality control teams to ensure adherence to quality standards and regulatory requirements
  • Drive continuous improvement initiatives through Lean and Kaizen methodologies.
  • Partner with Quality and Regulatory to ensure consistent operational excellence across external partners.
  • Ensure that manufacturing processes (including packaging and labeling) are suitable for distribution
  • Plan, coordinate, and execute manufacturing projects, ensuring timely completion within budgetary constraints
  • Develops and supports Standard Operating Procedures/Work Instructions with internal requirements to ensure regulatory and quality compliance.
  • Partner with supply chain and finance to track cost saving initiatives, cost- of poor quality, or cost per unit improvements.
  • Develop and maintain project plans, schedules and trackers for design transfer, process validation, and automation projects.
  • Participate in supplier audits and support CAPA investigations related to outsourced production.
  • Ensure manufacturing documentation aligns with FDA (21 CFR Part 13485, and company QMS requirements.

Qualifications

  • Proficiency with Microsoft office suite (PowerPoint, Excel, Word, etc.) and Windows
  • Analytical mindset with the ability to use data and information to drive decisions
  • The ability to communicate internally to all levels of the organization and externally with suppliers
  • Candidates are preferred that have experience managing medium sized projects as a Project Manager in Manufacturing (Medical or Non-Medical, but Medical is preferred).
  • Strong knowledge of FDA (21 CFR Part 820) ISO 13485, GMP and QMS documentation standards)

Skills & Experience

  • Bachelor’s degree in Engineering, Business Administration, Supply Chain, Logistics or related field, or an equivalent level of experience
  • 5-7 years of experience in manufacturing or relevant experience
  • Demonstrated ability to apply Lean, Kaizen, or Six Sigma methodologies (Certification preferred)
  • Bilingual in Spanish and English is a plus

Compensation & Benefits:

The anticipated salary range for this position is $90,000 - $120,000 annually. The actual pay rate will vary based on applicant’s location, education, relevant experience, skills, and education. This role is eligible for bonus and/or performance-based incentives.

LSL Healthcare offers a competitive salary, performance-based incentives, and a comprehensive benefits package, including health insurance, dental, vision, life, short- term and long-term disability, AD&D insurance, and 401(k) savings plan with employer match, paid time off and holiday pay, as well as professional development opportunities.

LSL Healthcare is an equal opportunity employer and prohibits discrimination and harassment of any kind. All applicants will be considered for employment without regards to race, color, religion, age, sex, sexual orientation, gender identity, national origin, veteran or disability status, or any other status protected by law. LSL is committed to cultivating a culture of diversity and inclusion promoting teamwork.

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SAP Manufacturing Architect

New
60060 Mundelein, Illinois YASH Technologies

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Job Description

The S4 HANA MFG stream encompasses all manufacturing processes. Not only will you provide support for the S4 HANA MFG business processes, you will also share your expertise in the end-to-end supply chain process and its key integration with EWM, Supply chain/MM and finance.


Bachelor’s Degree in Computer Science or Manufacturing area are required.

At least 15 years total SAP systems experience

At least 3 implementations on SAP S4 system leading MFG workstream

Strong functional and business knowledge in different SAP MM & PP modules.

Basic knowledge of EDI functions and usages.

Experienced with SAP MM & PP master data is required.

Past experience in SAP Fiori is preferred.

Experienced with labelling software such as OpenText, Document Presentment a plus.

Strong communication skills - both written and verbal.

Strong analytical and problem-solving skills.

Excellent interpersonal skills in areas such as teamwork, facilitation, and negotiation

Skilled at influencing, guiding and facilitating stakeholders and peers with decision making.

Good understanding of strategic and emerging technology trends, and the practical application of those technologies to evolving business and operating models

Ability to organize & balance multiple projects/priorities

Must be self-motivated with capability to work independently.

Ability to estimate the financial impact of technology alternatives

Trusted and respected as a thought leader who can influence and persuade business and IT leaders and IT development teams

Availability for 10-15% overnight domestic travel.

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