Engineering Journal Jobs in Beach Park Illinois

Job Title: Packaging Engineer

Location: North Chicago, IL

Hire Type: Open-ended Contract, Onsite

Target Pay Rate: $40.00 - $45.00/hour (W2)

Benefits: PTO, paid holidays, BCBS Medical plans, Dental/Vision plans, 401(k), and ESOP

Must-Have Skills:

• Packaging design & development experience (materials, structures, functionality)
• Packaging testing & validation expertise (performance, shipping, integrity)
• Manufacturing/plant experience (trials, troubleshooting, production support)

Job Summary:

The Packaging Engineer develops and implements packaging solutions for new and existing products, ensuring functionality, cost-effectiveness, and compatibility with manufacturing. This role supports pharmaceutical and/or combination product packaging through design, testing, validation, and cross-functional collaboration.

Job Duties:

• Design and develop primary, secondary, and tertiary packaging solutions
• Create and maintain packaging documentation (BOMs, specs, assembly instructions)
• Lead packaging validation and ensure compliance with FDA regulations (21 CFR 201, 210, 211)
• Develop and execute testing protocols (performance, container/closure integrity, shipping)
• Conduct plant trials, analyze results, and make recommendations on packaging viability
• Evaluate new materials and technologies to improve performance, cost, and efficiency
• Collaborate with internal teams and external suppliers to meet project timelines
• Support labeling, artwork review, and packaging design verification
• Troubleshoot packaging issues and support manufacturing operations

Qualifications:

• Bachelor's degree in Packaging Science, Packaging Engineering, or related field
• 2+ years of packaging design experience.
• Strong knowledge of packaging materials (corrugate, plastics, cartons, films) and testing methods
• Experience with packaging validation, documentation, and regulatory requirements
• Familiarity with manufacturing processes and packaging equipment (e.g., form-fill-seal)
• Ability to create 2D drawings
• Experience with pharmaceutical or combination product packaging is a plus.

Manufacturing Operations Manager

Our Manufacturing Operations Manager oversees execution of manufacturing, and production for the plant which includes safety, productivity, labor, cost, production schedule, quality, and continuous process improvements to meet established business goals. Plans and coordinates efficient and economical manufacturing activities and provides quality levels and service that exceed the customer’s expectations. Responsible for driving key initiatives to ensure cost reduction, inventory management, delivery performance, and key performance indicator (KPI) targets.

What will you be doing -

• Oversee and manage all manufacturing activities to ensure safety, quality, cost, and morale and to meet and exceed customer and Company requirements.
• Assist General Manager in the development and management of annual plan, budget, operating and capital expense budgets, Key Performance Indicators (KPI), operating efficiency, and cost control.
• Coordinate and guide activities in the areas of manufacturing, Lean, 5S, quality enhancements, staffing, training, and employee relations. Manage production supervisors.

What are we looking for -

• Bachelor’s Degree in Manufacturing, Industrial, or Operations Management; Mechanical, Industrial or Manufacturing Engineering; Supply Chain; Business Administration; or related field preferred but not required.
• 7-10+ years of manufacturing (i.e., assembly, cutting, fabrication, welding, painting, etc.) experience.
• 5+ years of progressively responsible manufacturing supervision/management experience.
• Practical experience applying Lean, Continuous Improvement, and Total Quality Production System (TQPS) principles in a manufacturing environment preferred.
• Experience with manufacturing and production KPIs/Analytics including the Production Efficiency (PEFF) system preferred.
• Experience with ERP/MRP systems and integrated computer programs and applications.

4Front Engineered Solutions is a leader in the door and docking industry. This role supports High Performance Doors, under the brand names Dynaco, Albany, and TKO, on-site at our Kenosha, WI facility.

What we offer -

• Medical, dental and vision insurance (HSA includes company contribution)
• STD, LTD, Life and AD&D insurance
• 401k including company match
• Variable compensation bonus plan paid out quarterly
• Reimbursement for select PPE
• 11 paid holidays
• 3 weeks of PTO per year, accrued with each bi-weekly payroll cycle

Why apply?

• Empowerment: You’ll work as part of a global team in a flexible work environment, learning and enhancing your expertise.
• Innovation: You embrace challenges and want to drive ambitious change.
• Integrity: You are results-oriented, reliable, straightforward and value being treated accordingly.

If you are interested or know someone who may be interested in working for a premier employer or want more information, please contact John Vandenberg at , 262-496-5374.

We are seeking a hands-on, detail-oriented Quality Supervisor to lead quality assurance and inspection efforts within a fast-paced manufacturing environment. This is a high-impact leadership role for someone who thrives on driving quality standards, developing strong teams, and improving processes that directly impact product performance and customer satisfaction.

If you’re passionate about building a culture of accountability, continuous improvement, and operational excellence, this is an outstanding opportunity to make a visible impact.

This is more than a traditional quality leadership role — it’s a chance to step into a highly visible position within a growing manufacturing organization that is backed by a major industry player and investing heavily in its future. With strong momentum, expanding capabilities, and a clear path for growth, this role offers the opportunity to make a measurable impact while helping shape the next chapter of the business.

What You’ll Do

As the Quality Supervisor, you will oversee day-to-day quality operations across the manufacturing process and ensure products meet rigorous internal and external standards. You’ll partner cross-functionally with production, engineering, and operations teams to resolve issues, improve systems, and elevate overall quality performance.

Key Responsibilities

• Lead and coordinate quality assurance and inspection activities across manufacturing operations
• Supervise a team of quality inspectors, technicians, and team leads across multiple shifts
• Ensure compliance with ISO 9001, ISO 14001, and other applicable quality standards
• Develop, implement, and maintain quality control procedures, systems, and documentation
• Conduct internal audits and help prepare for external audits and inspections
• Drive root cause analysis on non-conformances and lead corrective/preventive actions (CAPA)
• Partner with cross-functional teams to quickly resolve quality issues and improve outcomes
• Maintain inspection records and quality documentation with a high level of accuracy
• Train team members on quality systems, inspection methods, and regulatory requirements
• Identify and implement process improvements that enhance product quality and operational efficiency
• Support and enforce plant safety standards and best practices

What We’re Looking For

We’re looking for a leader who can balance technical quality expertise with strong people leadership. The ideal candidate brings a solid foundation in manufacturing quality systems, understands how to work across teams, and knows how to create structure and accountability on the floor.

Preferred Qualifications

• 3+ years of supervisory experience in a manufacturing environment
• 5+ years of experience working with ISO 9001 quality systems
• Experience leading quality assurance, inspection, or quality systems in a production setting
• Strong experience with root cause analysis, non-conformance resolution, and CAPA processes
• Ability to read and interpret blueprints, technical drawings, machining drawings, and CAD models
• Experience with ERP systems and strong working knowledge of Excel
• Hands-on experience using precision inspection equipment such as:
• CMM
• 3D scanners
• Calipers
• Gauges and other metrology tools
• Strong communication skills with the ability to lead teams and collaborate cross-functionally
• High school diploma required; bachelor’s degree in Engineering, Quality, Business, or a related field preferred
• Relevant quality certifications are a plus

Responsible for the safe maintenance of park rides, machinery and equipment.

Full-Time, Year Round, Hourly, paid weekly

Perks:

• Benefit options include, but are not limited to: Medical, Dental, Vision, Accident Insurance, and Group Auto and Home
• Retirement Benefits Include: 401K & Roth 401K
• Exclusive Employee Perks and Pricing for Season Passes and Tickets

• Perform visual inspections of assigned rides and attractions
• Perform rehab work on theme park rides and attractions
• Maintain, erect, repair and trouble-shoot various theme park rides and attractions
• Visually inspect and listen to machines and equipment to locate causes of malfunctions
• Remove and/or replace worn or defective parts using hand and/or power tools
• Perform routine preventative maintenance on various equipment including rides and attractions
• Keep a daily duty log of maintenance work performed as well as accurate records of preventative maintenance

• Should possess practical skill and proficient knowledge in two or more trades, such as: mechanical, electrical, electronics, hydraulics, pneumatics, carpentry, welding and small combustion engine repair and maintenance
• Must be able to trouble-shoot clearly, calmly and safely in the presence of Guests and fellow Team Members
• Should have strong mechanical, electrical & hydraulic experience
• Must possess strong safety sensitivity & ability to work with many different types of mechanical devises
• Must be able to read, write, speak and understand English
• Must possess the mental and physical capacities necessary to perform the primary job duties, including climbing and working at heights up to and in excess of 150ft., crawling and working in confined spaces and lifting up to 100 lbs. Must be able to work outdoors in extreme temperatures. Must possess the physical dexterity to operate hand tools and motor vehicles
• Must have tools and equipment to perform required duties and tasks as assigned
• Must possess a valid Driver's License
• Must be 18 years or older

• 
  
• Interface with vendors, OEM, and internal service organizations to address laboratory equipment service needs.
  
• Assist R&D personnel with selection and purchase of laboratory equipment and services.
  
• Provide administrative support throughout equipment lifecycle (onboarding, maintenance/repair, decommissioning).
  
• Serve as liaison to on-site vendor service personnel.
  
• Receive incoming work requests and generate workorders on demand.
  
• Process work orders and contracts within IBM Maximo system to ensure equipment status, service activities, and all cost of ownership expenses are properly documented.
  
• Maintain equipment warranty and service contract data within Maximo system and Access database.
  
• Process service contract renewals, including review of equipment reliability histories, determination of insourcing potential, and overall assessment of cost benefits.
  
• Work with department leadership to develop and refine processes in support of department functions.
  

• 
  
• College Degree or equivalent experience. A technical degree (Engineering or Science) is preferred.
  
• Knowledge of basic regulatory requirements, laboratory safety, and GxP.
  
• At least 2+ years of experience with a variety of laboratory equipment, either having served as a lab analyst, lab equipment service provider, or both.
  
• Effective written and oral communication skills capable of accommodating a diverse audience.
  
• Proficient in data entry, analysis, and presentation, particularly within Maximo, Cognos, and SAP environments.
  
• Attention to detail, strong organization and planning skills.
  
• Capable of independently developing creative solutions in a fast-paced environment.
  
• Self-motivated and positive attitude with a great desire to contribute to our success.
  

A leader in technology and innovation, Southwire Company, LLC is one of North America’s largest wire and cable producers. Southwire and its subsidiaries manufacture building wire and cable, utility products, metal-clad cable, portable and electronic cord products, OEM wire products and engineered products.

Value Stream Manager Summary

The Value Stream Manager is a leadership role that will be primarily focused on ensuring a safe work environment for all team members, while maintaining continuous operational execution and production of quality products that are delivered on-time to customers within established cost targets.

The Value Stream Manager will focus on eliminating waste developed in the value stream process, identifying business growth opportunities, understanding the importance of customer value created by the company, maximizing capacity to grow sales and driving lean continuous improvement.

Strategically focused and leading/driving team members in Kaizen events, problem solving activities, owning the value stream.

Key Responsibilities

• Manage all value stream related KPIs (SQDCI).
• Co-leads recordable or significant case investigations including root-cause and corrective actions.
• Responsible for ensuring the execution of findings of accident investigations and safety alerts within their value stream.
• Ensure policies and processes are deployed uniformly throughout the value stream.
• Actively leads the daily huddle process and can share information related to value stream as needed.
• Lead problem solving events and follow-up with corrective actions for completion
• Create a standard for value stream process and ensure entire team are properly trained, resourced, supplied, and managed to attain the objectives
• Develop a highly motivated and committed workforce with emphasis on the development of skills needed to accomplish safety, quality, on-time delivery, and product cost goals.

Qualifications And Experience Requirements

• Bachelor’s degree is required
• 5+ years of management experience
• Bilingual is a plus
• Lean manufacturing experience is required
• Strong MS Excel experience desired
• SAP is preferred

Benefits We Offer:

• 401k with Matching
• Family and Individual Insurance Packages (Health, Life, Dental, and Vision)
• Paid Time Off & Paid Holidays
• Long & Short-Term Disability
• Supplemental Insurance Plans
• Employee Assistance Program
• Employee Referral Program
• Tuition Reimbursement Programs
• Advancement & Professional Growth opportunities
• Parental Leave
• & More

Southwire is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

Role: MEP Engineer – Capital Projects

Location: North Chicago, IL/Milwaukee, WI/Indianapolis, IN

Duration: 12+Months(Contract#W2)

Client: Pharmaceutical

Objective:

Ensure all mechanical, electrical, and plumbing (MEP) installations meet the approved design, performance standards, and regulatory requirements through inspection, verification, and proper documentation.

Key Responsibilities:

Electrical Systems

• Inspect electrical equipment, wiring, and installations to ensure compliance with approved designs and regulations.
• Review instrument calibration certificates and loop testing documents.
• Check instrument air systems, tubing, and junction box installations.
• Verify grounding, bonding, and safety disconnect systems.
• Inspect motor control centers (MCC), variable frequency drives (VFD), and power distribution systems.
• Review electrical documentation and as-built drawings.

Mechanical Systems

• Inspect mechanical equipment and installations to ensure compliance with approved designs and regulations.
• Review mechanical drawings, specifications, and documentation.
• Monitor mechanical construction progress and quality.
• Review mechanical as-built documentation.

Quality & Compliance

• Review design documents, technical drawings, and layouts against project requirements (URS).
• Document construction progress and quality observations.
• Identify and report deviations or non-conformities.
• Inspect damaged materials and report issues.
• Schedule and conduct site inspections.

Coordination & Reporting

• Attend project meetings as required.
• Collaborate with engineering, QA, contractors, and suppliers to resolve issues.
• Provide inspection feedback and corrective action recommendations.
• Maintain and share earned value/credit reports with project stakeholders.

Kindly share resume at or call me at 678-935-7045 to discuss more!

Job Title: Deviation Investigation Writer/Associate

Location: Pleasant Prairie, WI

Duration: 3-Month Contract (Potential of Extension)

Overview:

We are seeking two detail-oriented and driven professionals to join a dynamic manufacturing

operations team as Deviation Investigation Writers. These individuals will play a critical role in

supporting quality compliance by documenting and investigating deviations—unexpected events that

impact product quality, safety, or regulatory standards.

Key Responsibilities:

• Ghostwrite deviation investigation reports on behalf of technical staff, including operators and engineers.
• Collaborate with subject matter experts to gather information and draft clear, audit-ready documentation.
• Support root cause investigations (RCI) and contribute to continuous improvement efforts.
• Assist in managing deviations across various manufacturing areas, including filling, inspection robotics, and process operations.
• Ensure documentation meets regulatory standards and is easily understandable by auditors and cross-functional teams.

Required Qualifications:

• Proven experience in technical writing, preferably in a regulated or manufacturing environment.
• Background in quality assurance, engineering, or a related technical field.
• Ability to quickly learn complex manufacturing processes and translate them into clear, structured documentation.
• Strong analytical and communication skills.
• Comfortable working independently and collaboratively in a fast-paced setting.

Preferred Qualifications:

• Experience writing deviation investigation reports or supporting root cause analysis.
• Familiarity with manufacturing environments such as pharmaceutical, chemical, or food production.
• Understanding of parenteral manufacturing processes is a plus, but not required.