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Medical Device Operations Jobs in Cary, IL (NOW HIRING)

We are seeking an experienced and results-driven Operations Manager to oversee the operations of our plastic injection molding facility specializing in the production of medical device components.

Research Scientist

Lake Zurich, IL ยท On-site

$120 - $180/hr

Experience in an FDA-regulated laboratory environment in the drug and medical device industries, including GMP/GLP/GDP operations * Ability to perform analytical laboratory testing and demonstrate ...

New

Engineering Manager, NPI

Wheeling, IL ยท On-site

$135 - $150/hr

Viant is a global medical device partner providing design, development, manufacturing, and assembly ... The NPI Engineering Manager will partner closely with customers, Operations, Quality, Manufacturing ...

New

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

Quality Technician II

Lake Zurich, IL ยท On-site

$24 - $36/hr

... a privately owned medical device company specializing in the development, testing, and ... Ability to communicate effectively with Engineering, Quality, and Operations teams. * Good hand-eye ...

Showing results 21-40

Medical Device Operations information

See Cary, IL salary details

$11

$26

$54

How much do medical device operations jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for medical device operations in Cary, IL is $26.62, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $30.72 per hour, depending on experience, location, and employer.

What is medical device operations?

Medical device operations refer to the processes and activities involved in the manufacturing, assembly, quality control, supply chain management, and distribution of medical devices. This field ensures that devices are produced efficiently, meet regulatory standards, and are delivered safely to healthcare providers and patients. Operations teams collaborate with engineering, quality assurance, and regulatory departments to maintain compliance and optimize production workflows. Their work is crucial for ensuring that medical devices are safe, effective, and readily available for patient care.

What are the key skills and qualifications needed to thrive in medical device operations?

To thrive in Medical Device Operations, you need a solid understanding of regulatory compliance, quality assurance, and supply chain management, often supported by a degree in engineering, life sciences, or business. Familiarity with quality management systems (QMS), FDA regulations, and software like ERP systems is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring compliance. These competencies are vital for delivering safe, high-quality medical devices efficiently and in accordance with rigorous industry standards.

What are some common challenges faced by professionals in medical device operations, and how can they be addressed?

Professionals in Medical Device Operations often face challenges related to maintaining strict regulatory compliance, ensuring product quality, and managing cross-functional communication between manufacturing, quality assurance, and regulatory teams. Staying up to date with changing FDA or international regulations is essential, and frequent documentation or process audits can be demanding. Building strong organizational habits, leveraging digital tracking tools, and fostering open communication channels with other departments can help address these challenges and ensure smooth operations.

What is the difference between Medical Device Operations vs Medical Device Quality Assurance?

AspectMedical Device OperationsMedical Device Quality Assurance
Primary FocusManaging manufacturing, supply chain, and product deploymentEnsuring product quality, compliance, and safety standards
Required CertificationsRegulatory knowledge, manufacturing certificationsQuality management certifications, ISO standards
Work EnvironmentManufacturing plants, supply chain settingsQuality labs, compliance departments
Industry UsageUsed across production and logistics teamsUsed within quality control and regulatory teams

Medical Device Operations and Medical Device Quality Assurance roles often overlap but focus on different aspects of the product lifecycle. Operations centers on manufacturing and logistics, while Quality Assurance emphasizes compliance and safety. Both roles require regulatory knowledge and are essential in the medical device industry.

What job categories do people searching Medical Device Operations jobs in Cary, IL look for?

The top searched job categories for Medical Device Operations jobs in Cary, IL are:

What cities near Cary, IL are hiring for Medical Device Operations jobs?

Cities near Cary, IL with the most Medical Device Operations job openings:

Infographic showing various Medical Device Operations job openings in Cary, IL as of August 2026, with employment types broken down into 86% Full Time, 6% Part Time, and 8% Contract. Highlights an 89% In-person, 8% Hybrid, and 3% Remote job distribution, with an average salary of $55,374 per year, or $26.6 per hour.

Operations Manager

MRINetwork Jobs

Buffalo Grove, IL โ€ข On-site

Other

Re-posted 4 days ago


Job description

Operations Manager

Our partner is a diversified manufacturing partner of choice that helps market-leading brands design, build, and deliver innovative products that improve the world.

A career here offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.

Position Summary:

We are seeking an experienced and results-driven Operations Manager to oversee the operations of our plastic injection molding facility specializing in the production of medical device components. This position is responsible for managing the overall production function, while collaborating with program management, quality assurance, engineering, maintenance, and supply chain functions to ensure compliance with ISO 13485, FDA regulations, and internal quality standards. The ideal candidate will possess strong leadership skills, deep manufacturing knowledge, and a commitment to continuous improvement and regulatory compliance.

Key Responsibilities:

·       Oversee daily operations of injection molding production to meet or exceed safety, quality, delivery, and cost goals.

·       Ensure compliance with all regulatory and quality system requirements (e.g., ISO 13485, FDA cGMP).

·       Develop and implement operational policies, procedures, and best practices.

·       Collaborates with management, production, and the commercial team to evaluate manufacturing feasibility leading to quote compilation for new and existing products.

·       Forecasts operating costs of the department and directs preparation of budget requests.

·       Partners with team and management in the development of the strategic plan and Annual Operating Plan (AOP) for the function.

·       Reviews and establishes material, equipment, and manpower resource requirements.

·       Prioritizes production schedules based on product introduction, equipment efficiency, and materials supply to meet customer requirements.

·       Coordinates production activities with other functional groups, such as planning and distribution.

·       Selects and develops personnel to ensure the efficient operation of the production function.

·       Accountable for controlling manufacturing operations, and ensuring that production quality and cost targets are met.

·       Develop customer relationships to be the partner of choice.

·       Plan, organize and lead production ramps to meet customer demand increases.

·       Drive continuous improvement initiatives using Lean, 5S, KAIZEN and other methodologies.

·       Explores technology trends and market demand to plan projects.

·       Collaborate with Engineering on design for manufacturability (DFM), mold validation, and new product introduction (NPI).

·       Manage staffing, training, performance reviews, and development of team members

·       Monitor KPIs and use data to identify areas for improvement in efficiency, scrap reduction, and downtime.

·       Oversee plant scheduling, capacity planning, and resource allocation.

·       Ensure proper preventive maintenance and readiness of molding equipment and tooling.

·       Coordinate with supply chain and procurement teams to ensure material availability and inventory optimization.

Qualifications:

Required:

·       Bachelor’s degree in Engineering, Operations Management, or related field.

·       Minimum of 7 years’ experience in a manufacturing leadership role, with at least 5 years in plastic injection molding.

·       Strong knowledge of medical device manufacturing standards and regulations (ISO 13485, FDA 21 CFR Part 820).

·       Demonstrated experience with Lean Manufacturing and/or Six Sigma methodologies.

·       Strong leadership, problem-solving, and organizational skills.

·       Excellent communication and interpersonal abilities.

·       Demonstrates detailed expertise in very complex functional/technical area or broad breadth of knowledge in multiple areas; understands the strategic impact of the function across sites.

·       Demonstrates advanced people and/or process management skills as well as customer (external and internal) relationship skills.

·       Demonstrates knowledge of multiple functional technologies/processes, industries or functions, and understanding of interdependencies of such processes at the site.

·       To perform the major job responsibilities the use of the following tools may be required: Office Skills: telephones, word processing, spreadsheet (PC), presentation, and database software.

Preferred:

·       Certification in Six Sigma (Green Belt or higher), PMP, or Lean.

·       Experience with Class I, II, or III medical device manufacturing.

·       Scientific Injection molding process knowledge

Working knowledge of molds and tool maintenance