Engineering Jobs in Indian Creek, IL

38 positions found

Senior Quality Engineer
✦ New
Salary not disclosed
Barrington, IL 6 hours ago

Senior Quality Engineer

Location: Near Barrington, IL

Hire Type: Direct Hire

Salary: $90,000–$105,000/year

Benefits: Medical, Dental, Vision, 401(k) with Match, Life Insurance, Tuition Reimbursement, PTO, Paid Holidays


Sterling Engineering is partnering with a growing manufacturing organization to hire a Senior Quality Engineer to support quality systems, investigations, and continuous improvement initiatives across a diverse set of industries, including aerospace, automotive, medical, energy, robotics, and industrial equipment.

This is a high-impact role for someone who enjoys working cross-functionally, driving quality improvements, and solving complex manufacturing challenges in a fast-paced environment.


Key Responsibilities

  • Lead continuous improvement and quality-focused projects across manufacturing operations
  • Apply statistical analysis to evaluate production data and drive process improvements
  • Partner with internal teams and customers to resolve quality concerns, complaints, and non-conformances
  • Drive corrective actions from root cause through implementation and validation
  • Support inspection and quality teams with investigations and material disposition
  • Conduct internal, customer, and supplier audits as needed
  • Utilize tools such as SPC, gage R&R, process capability, regression, and ANOVA to improve manufacturing performance
  • Facilitate structured problem-solving using 5-Why, fishbone diagrams, and other methodologies


Qualifications

  • Bachelor’s degree in Mechanical Engineering, Industrial Engineering, or related field
  • 5–8+ years of experience in a manufacturing quality environment
  • Experience working with quality standards such as IATF 16949, ISO 13485, and/or AS9100
  • Strong knowledge of APQP, PPAP, FMEA, Control Plans, and QMS processes
  • Proven experience with corrective actions, root cause analysis, and continuous improvement initiatives
  • Proficiency with statistical analysis tools and data-driven decision making
  • Experience conducting internal QMS audits
  • Background in automotive, aerospace, or medical manufacturing preferred
  • Strong communication skills with the ability to collaborate across teams and with external customers
Not Specified
Clinical Project Manager I – Clinical Supply Chain
✦ New
Salary not disclosed
Lake Bluff, IL 6 hours ago
Clinical Project Manager I – Clinical Supply Chain
North Chicago, IL (Onsite Required)
Contract: 12 months (potential to extend)
Rate: $43–$47/hour (based on benefit selection)

Orion Group is seeking a Clinical Project Manager I to support Clinical Supply Chain activities for our pharmaceutical client in North Chicago.

This role is responsible for managing clinical supply activities at the protocol level across Phase I–IV clinical trials, ensuring investigational drug supplies and related materials are delivered to global clinical sites on time and in compliance with regulatory requirements.

This is an excellent opportunity for professionals with experience in clinical development, supply chain, or pharmaceutical project management who are interested in supporting global clinical trial operations.
 
Key Responsibilities
  • Manage clinical supply chain activities at the clinical protocol level for Phase I–IV clinical trials
  • Coordinate forecasting, planning, scheduling, and execution of investigational drug supply distribution to clinical sites and depots
  • Collaborate with Clinical Study Teams to support protocol design and optimize clinical supply planning
  • Translate clinical study design requirements into packaging and labeling strategies
  • Author the study medication and labeling sections of clinical protocols
  • Develop protocol-specific labeling compliant with global regulatory requirements
  • Create and manage project timelines, milestones, and supply logistics plans
  • Conduct scenario analysis and develop risk mitigation and contingency plans for clinical supplies
  • Forecast protocol-specific drug product requirements including comparators, ancillary supplies, and clinical trial commodities
 
 
Required Qualifications
  • Bachelor’s degree required, preferably in:
    – Physical or Biological Sciences
    – Chemistry or Pharmacy
    – Engineering
    – Mathematics
  • 2+ years of experience within the pharmaceutical industry
Preferred experience in one or more of the following areas:
  • Drug discovery (Process Chemistry, Analytical Chemistry)
    • Drug development (Formulation)
    • Clinical operations / Clinical project management
    • Clinical supply chain management
    • Quality Assurance in regulated environments
 
Key Skills & Competencies
  • Understanding of clinical development and global clinical supply chain processes
  • Knowledge of regulatory compliance, SOPs, and GxP environments
  • Strong project management and organizational skills
  • Ability to manage multiple priorities and timelines in a fast-paced environment
  • Effective cross-functional collaboration with teams including Clinical Operations, Quality Assurance, Analytical, and Supply Chain
  • Strong written and verbal communication skills
 
Ideal Candidate Profile
The ideal candidate will have experience working in clinical trials, pharmaceutical development, or clinical supply chain management, and will be comfortable coordinating cross-functional teams to ensure investigational product supplies are delivered efficiently and compliantly to clinical sites.

People are our business worldwide
 
Orion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.

Not Specified
Product Manager
✦ New
🏢 Sterling Engineering
Salary not disclosed
Vernon Hills, IL 6 hours ago

Product Manager


Compensation & Benefits

  • Salary: $110,000 – $130,000 + Annual Bonus
  • Medical, Dental, Vision Coverage
  • 401(k) with Company Match


About the Opportunity

Sterling Engineering is partnering with a leading organization to hire a Product Manager who will drive innovation, profitability, and strategic growth across a diverse product portfolio.

This role is ideal for a data-driven, strategic thinker who thrives in retail manufacturing or industrial product environments and enjoys balancing high-level strategy with hands-on execution. You’ll play a key role in shaping product direction—not just responding to customer requests, but proactively identifying opportunities that impact the broader market.


What You’ll Do

Product Strategy & Portfolio Management

  • Lead product innovation through competitive analysis, gap identification, and market insights
  • Manage and optimize product portfolios, including SKU rationalization and lifecycle management
  • Identify new product opportunities aligned with business goals and market demand
  • Own product data and performance metrics to drive strategic decision-making
  • Partner with Supply Chain and Manufacturing to refine product specs, cost structures, and procurement strategies

New Product Development

  • Develop and execute product roadmaps focused on innovation and value creation
  • Collaborate cross-functionally to ensure successful product launches and market adoption
  • Support continuous improvement initiatives across multiple product lines

Pricing Strategy

  • Analyze market trends and competitor pricing to ensure optimal positioning
  • Implement pricing strategies that drive both revenue growth and margin expansion
  • Conduct pricing analysis and experiments to evaluate demand and profitability

Channel & Go-to-Market Strategy (Place & Promotion)

  • Define and optimize sales channels (distribution, e-commerce, dealer networks, etc.)
  • Partner with Marketing to develop promotional strategies, campaigns, and product positioning
  • Support merchandising, packaging, and product content strategies across channels
  • Build and manage promotional calendars aligned with key sales events and market opportunities

What We’re Looking For

  • 3–5+ years of Product Management experience with a focus on strategy, innovation, and analytics
  • Experience in retail manufacturing, industrial, or durable goods environments
  • Strong background in competitive analysis, pricing strategy, and portfolio management
  • Proven ability to influence internal product strategy at scale, beyond individual customer requests
  • B2B experience preferred
  • Bachelor’s degree required (Master’s preferred)
  • Excellent communication, leadership, and cross-functional collaboration skills
  • Demonstrated career stability and long-term impact in prior roles
Not Specified
Packaging Engineer
✦ New
🏢 Sterling Engineering
Salary not disclosed

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.
Not Specified
Tool Crib Supervisor
✦ New
🏢 LHH
Salary not disclosed
Barrington, IL 6 hours ago

Job Title: Tool Room Manager

Location: Barrington, IL

Salary: $105,000-$128,000


LHH Recruitment Solutions is currently seeking a Tool Room Manager to join our client's organization in the Barrington, IL area.


Key Responsibilities:

  • Lead and manage daily operations of the tool room, ensuring efficient support of manufacturing and production needs.
  • Plan, schedule, and coordinate tooling workloads, personnel, and resources to meet production schedules and delivery commitments.
  • Track and analyze tooling costs, labor efficiency, and time spent to support continuous improvement and cost control.
  • Oversee preventive maintenance programs for tooling, dies, molds, and tool room equipment to ensure reliability and uptime.
  • Recommend and implement improvements to tooling processes, workflows, and equipment to enhance quality, efficiency, and safety.
  • Support new product introductions by assigning tooling work, monitoring progress, and resolving start‑up issues.
  • Lead and support lean manufacturing initiatives, including 5S and continuous improvement activities within the tool room.
  • Manage inventory and stock control of tooling, components, and supplies.
  • Ensure compliance with quality systems, safety standards, and applicable regulatory requirements.
  • Supervise, coach, and develop tool room staff, including performance management and workforce planning.

Key Qualifications:

  • Experience managing a tool room or similar technical manufacturing function in a production environment.
  • Strong background in tool and die, machining, stamping, molding, or related manufacturing processes.
  • Demonstrated leadership experience supervising skilled trades or technical teams.
  • Knowledge of preventive maintenance practices for dies, molds, and tooling equipment.
  • Familiarity with lean manufacturing principles, including 5S and continuous improvement methodologies.
  • Working knowledge of inventory control, cost tracking, and production scheduling.
  • Ability to interpret blueprints, technical drawings, and specifications.
  • Experience with quality systems and standards such as ISO or IATF preferred.
  • Strong problem‑solving, communication, and organizational skills.
  • Technical education, journeyman training, or a degree in engineering or a related field preferred.

Benefits:

  • Medical, Dental and Vision
  • 2 Weeks PTO (negotiable) & Paid sick leave where applicable by state law
  • 401(k)
  • HSA and FSA
  • Life and AD&D
  • STD and LTD
  • Norton LifeLock

Equal Opportunity Employer/Veterans/Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act

• Los Angeles City Fair Chance Ordinance

• Los Angeles County Fair Chance Ordinance for Employers

• San Francisco Fair Chance Ordinance

Not Specified
Manufacturing Engineer
✦ New
🏢 Sterling Engineering
Salary not disclosed
Barrington, IL 6 hours ago

Title: Manufacturing Engineer

Location: Barrington, IL 60010

Hire Type: Direct Hire

Compensation: $115k-130k

Benefits: Medical, Dental, Vision, 401k, PTO, Holiday Pay, Retirement, Life Insurance, and many more….

Overview: Our client is seeking a Manufacturing Engineer for a highly visible role that is designed to evolve into a true subject matter expert position, with clear leadership potential over time. This is an opportunity to own complex manufacturing processes end-to-end, influence technical direction, and become a go-to resource across engineering and operations.


Key Responsibilities:

  • Serve as a technical authority for assigned manufacturing processes and product lines
  • Lead manufacturing process design, optimization, and validation for precision metal components
  • Drive Lean manufacturing and continuous improvement initiatives (yield, cycle time, scrap, cost)
  • Partner cross-functionally with Design Engineering, Quality, and Operations on new product introductions
  • Develop and improve tooling, fixturing, work instructions, and standard processes
  • Troubleshoot complex manufacturing and quality issues using data-driven root cause analysis
  • Support capacity planning, capital equipment justification, and implementation
  • Mentor junior engineers and technicians; contribute to long-term technical strategy
  • Gradually take on informal and formal leadership responsibilities as the role matures

Qualifications:

  • Bachelor’s degree in Mechanical, Manufacturing, or Industrial Engineering (or similar)
  • 7+ years of manufacturing engineering experience in precision manufacturing environments
  • Strong background in metal forming, stamping, springs, or closely related processes preferred
  • Experience with Lean manufacturing, process optimization, and root cause analysis
  • Ability to operate as both a hands-on problem solver and strategic technical resource
  • Strong communication skills and comfort working cross-functionally
Not Specified
Quality Associate II
✦ New
🏢 Vantive
$80,000
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere.

For 70 years, our team has driven meaningful innovations in kidney care.

As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies.

Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre.

Each of us is driven to help improve patients’ lives worldwide.

Join us in advancing our mission to extend lives and expand possibilities.

Your Role: Responsible to ensure compliance with Regulatory, Corporate and Local Quality requirements and for providing Quality oversight of Vantive US and Canada warehousing and distribution operations, including internal warehouse site QA activities, internal renal fleet drivers, external warehousing partners (i.e., 3PL providers, wholesalers, freight forwarders and consolidation/ deconsolidation centers), and external transportation providers.

Oversight of distribution/warehouse-related external suppliers.

Act as a key partner with US and Canada Vantive Operations (including Supply Chain, Logistics and Fulfillment) to manage Quality requirements and oversight of all 3PL activities.

Responsible for compliance with FDA and Health Canada requirements, ISO standards and Vantive QMSby applying rigorous quality standards, including Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP).

What you'll be doing: Responsible for the implementation of Distribution QA activities to ensure compliance to FDA and Health Canada requirements.

This includes activities related to issue management (product dispositions, deviations, complaint investigations, holds), site QA management (pest control, temperature monitoring, returns, validation) and internal/supplier/3PL QA management (warehouses, internal private fleet, transportation carriers, suppliers impacting fulfillment).

Participate in discussions and on projects and cross-functional teams as required.

Support distribution and warehousing-associated external suppliers which includes audit support, supplier corrective action requests, quality/distribution agreements, new supplier requests, supplier notifications of change and change controls.

Work closely with UCAN planning and fulfillment organizations to meet business goals and objectives.

Facilitate and assist in GMP, ISO, US state distribution/pharmacy licensing and other internal/external audits and investigations pertaining to Vantive and/or 3PL facilities, where applicable.

What you'll bring: Able to manage multiple projects and/or responsibilities simultaneously   Support in meeting and exceeding quality key performance indicators (KPIs)          Solid understanding of FDA Regulations, Health Canada requirements and Application of Good Distribution Practices·          Must be proficient with Microsoft Office and other data collection/analysis programs (e.g.

Minitab) Excellent interpersonal/communication/presentation/negotiation skills Must have basic English written and oral communication skills adequate to connect with other team members        Initiative to be a subject matter expert in select processes and areas Supports ethical behaviors and decision-making Education and/or Experience: Bachelor’s Degree required (preferably in science, engineering or equivalent field) Minimum of 3 years of experience in Quality, or related field in the medical products/pharmaceutical industry Experience preferred for the following: distribution and warehousing in US and Canada, Quality Management Systems, FDA and Health Canada regulations, supplier quality Vantive is committed to supporting the need for flexibility in the workplace.

We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite.

This policy provides the benefits of connecting and collaborating in-person in support of our Mission.

We understand compensation is an important factor as you consider the next step in your career.

At Vantive, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

The estimated base salary for this position is $80,000 to $90,000 annually.

The estimated range is meant to reflect an anticipated salary range for the position.

We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change.

Individual pay is based on upon location, skills and expertise, experience, and other relevant factors.

This position may also be eligible for discretionary bonuses.

For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

US Benefits at Vantive This is where your well-being matters.

Vantive offers comprehensive compensation and benefits packages for eligible roles.

Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance.

Financial and retirement benefits include the Aon Pooled Employer Plan (“Aon PEP”), Vantive’s 401(k) retirement savings plan, to help you prepare for your future.  The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently.  The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals.

We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave.

Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits.

Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive’s US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Vantive Equal Employment Opportunity Vantive is an equal opportunity employer.

Vantive evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.                                                                                                                                                               Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information.

To learn how you can protect yourself, review our Recruitment Fraud Notice .
Not Specified
Operations Support III JP32786
✦ New
🏢 Orion Group
Salary not disclosed
Lake Bluff, IL 1 day ago
Operations Support III – Patient Services Operations
Location: Mettawa, IL 
Work Model: Hybrid – onsite approximately one week per month
Contract Duration: Through December 2026 (extension likely)
Rate: $21-26/HR based on benefit selection

Orion Group's pharmaceutical client is seeking an Operations Support III professional to join the U.S. Patient Services (APS) Operations team. The APS organization is recognized as an industry leader in delivering high-quality patient support programs that enhance both patient satisfaction and brand loyalty.

This role provides operational coordination, reporting, and project support to ensure efficient service delivery across APS initiatives. The position reports to the Director or Associate Director of APS Operations and collaborates closely with internal teams and external vendors.

Key Responsibilities

Operational Coordination
  • Coordinate onboarding and offboarding processes in partnership with internal stakeholders and external vendors
  • Support operational workflows to ensure continuity and efficiency of APS programs
Process Improvement
  • Identify and recommend process improvements and operational efficiencies within APS operations
  • Support initiatives that enhance workflow consistency and service delivery quality
Issue & Ticket Management
  • Monitor and manage tickets within a custom issue management system
  • Analyze trends, identify recurring issues, and support resolution efforts
Project & Reporting Support
  • Provide project management and operational support across APS initiatives
  • Develop and maintain routine reports using Microsoft Excel
  • Create PowerPoint presentations for leadership and stakeholder updates
Additional Support
  • Assist with special projects and ad hoc operational initiatives as assigned by APS Operations leadership
Required Qualifications
  • Strong written and verbal communication skills
  • High level of attention to detail and accuracy
  • Ability to manage multiple priorities in a fast-paced environment
  • Strong organizational and time management skills
  • Comfortable working across multiple systems and tools simultaneously
  • Proficiency in Microsoft Office, particularly Excel and PowerPoint
Ideal Candidate Profile
The ideal candidate is a highly organized operations professional who thrives in collaborative environments and enjoys supporting operational processes, reporting, and cross-functional initiatives.
Experience supporting healthcare, pharmaceutical, patient services, or operational teams is a plus.

People are our business worldwide
 
Orion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.

Not Specified
Director, Indirect Procurement
✦ New
🏢 LHH
Salary not disclosed
Vernon Hills, IL 1 day ago

LHH Recruitment Solutions has partnered with a growing organization, and they are seeking a motivated Director, Indirect Procurement to join their team. You will lead a large, enterprise-wide spend portfolio. This is a highly visible role for a procurement leader who thrives in hands-on, stakeholder-facing environments and brings deep expertise across transportation, logistics, facilities, and utilities categories. This position offers the opportunity to shape strategy while remaining closely embedded in the business—working directly with executive leadership, plant operations, and cross-functional partners to drive value, resilience, and long-term capability.


The Opportunity:

The Director of Indirect Procurement will own and lead a $1B+ annual indirect spend portfolio, with primary emphasis on:


  • Transportation and logistics (3PL – over-the-road and ocean).
  • Warehousing and distribution services.
  • Utilities, facilities, and site services.


This leader will be responsible for developing and executing sourcing strategies that balance cost, service, risk, and scalability across a multi-site manufacturing and operations footprint.


Key Responsibilities:

  • Lead enterprise-wide sourcing strategies across transportation, logistics, warehousing, utilities, facilities, and related indirect categories.
  • Act as a trusted business partner to senior executives and site leadership, ensuring procurement is fully embedded in core business decisions.
  • Drive total cost of ownership improvements while maintaining service continuity and supply assurance.
  • Lead complex supplier negotiations and long-term contractual strategies across domestic and international providers.
  • Build and maintain strong supplier relationships that enable innovation, flexibility, and performance improvement.
  • Partner closely with operations, finance, engineering, and HR to align procurement strategies with business objectives.
  • Develop and manage annual value creation targets, budgets, and performance metrics.
  • Ensure procurement governance, policies, and standards are consistently applied across the organization.


Leadership & Talent Development:

  • Lead, coach, and develop a high-performing indirect procurement team.
  • Play an active role in hiring, onboarding, and succession planning for procurement talent.
  • Establish clear performance expectations, development plans, and engagement rhythms.
  • Foster a hands-on, collaborative culture that values accountability, ownership, and continuous improvement.


Stakeholder Engagement:

  • Serve as a primary procurement interface to executive leadership and senior business stakeholders.
  • Navigate complex, sometimes competing priorities across multiple plants and functions.
  • Travel to manufacturing sites, vendors, and key stakeholders as needed (approximately 20–25%; majority of sites located in IL/WI).


Qualifications and Skills:

  • Bachelor’s Degree required; advanced degree (MBA or equivalent) preferred.
  • Significant, progressive leadership experience in indirect procurement within large, complex organizations.
  • Deep expertise in transportation procurement (3PL – over-the-road and ocean), warehousing, utilities, and facilities.
  • Proven experience managing and influencing large-scale spend portfolios (approaching or exceeding $1B annually).
  • Strong executive presence with the ability to influence, challenge, and partner at the senior leadership level.
  • Hands-on leadership style with a track record of being embedded in the business.
  • Experience supporting multi-site manufacturing, industrial, or asset-intensive environments.
  • Background in organizations with mature procurement and sourcing functions.
  • Exposure to international suppliers and global sourcing strategies.


Compensation Range: $200,000 - $240,000 + 25% Bonus


Benefits Offered: 3 weeks 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 Director, Indirect Procurementlooking for anew 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 free 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

Not Specified
Manufacturing Engineer II
✦ New
Salary not disclosed
Buffalo Grove, IL 1 day ago

Job Description


Who will you be working with?

You'll be joining Wabtec Bus Solutions, a team driving innovation in Transit Bus & Rail systems, including passenger door systems, wheelchair lifts & ramps, e-Bus charging systems, driver’s protective barriers, and more. We blend technical expertise with deep product knowledge to deliver high-impact solutions for our customers and communities.


How will you make a difference?

As a Manufacturing Engineer II within Wabtec Bus Solutions, you will perform a variety of manufacturing engineering assignments including developing, evaluating and improving manufacturing methods within the industrial plant. Estimate production times, staffing requirements, and related costs to provide information for management decisions. Confers with management, engineering, and other staff regarding manufacturing capabilities, and other considerations to facilitate production processes. Train technical as well as non-technical associations, assist others through moderate to complex tasks and apply statistical methods to estimate future manufacturing requirements and potential issues while driving solutions.


What do we want to know about you?

You may be a good fit if you have:

  • Bachelor's degree (B. S.) from four-year College or university; or three to six years related experience and/or training; or equivalent combination of education and experience.
  • Experience in Lean Manufacturing, FMEA, PFMEA ,Gemba events. Experience (6 months or more) in Auto-Cad, or ProE/ Solid Works is required.
  • Exceptional technical and problem-solving skills and reasoning capability
  • Must be a self-motivated and a great team worker


What will your typical day look like?

  • Quality Management - Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness.
  • Visionary Leadership - Displays passion and optimism; Inspires respect and trust; Mobilizes others to fulfill the vision; Provides vision and inspiration to peers and subordinates.
  • Cost Consciousness - Works within approved budget; Develops and implements cost saving measures; Contributes to profits and revenue; Conserves organizational resources.
  • Project Management - Develops project plans; Coordinates projects; Communicates changes and progress; Completes projects on time and budget; Manages project team activities.
  • Conduct DFMEA sessions to identify and mitigate design risks


What about the physical demands of the job?

  • Primarily office-plant based work
  • Use a computer for extended periods
  • Occasionally lift/move up to 25 pounds
  • Stand, walk, and navigate facilities
  • Occasional travel (10%) to customers and manufacturing sites


You may also be asked to perform other duties outside of your function or trade, for which adequate training will be provided if necessary.

Relocation assistance may be provided if eligibility requirements are met.

Wabtec will only employ those who are legally authorized to work in the U.S. for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable) and fitness for duty test (as applicable).


Additional Information

Our job titles may span more than one career level. The salary rate for this role is currently $6 The actual salary offered to a candidate may be influenced by a variety of factors, such as training, transferable skills, work experience, education, business needs, market demands and work location. The base pay range is subject to change and may be modified in the future. More information on offered benefits, which include health, welfare, and retirement, are available at . Other benefit offerings for this role may include annual bonus, if eligible.


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Not Specified
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