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Medical Device Program Manager Jobs in Kenosha, WI

Nemera

Program Manager

Buffalo Grove, IL · On-site

The headquarters and Innovation Center for early device design and development are located in ... Program Manager provides successful new and existing product introduction through effective ...

Foxconn WI

Program Manager

Mount Pleasant, WI · On-site

Program Management Employment Type: Full Time Location: SMC Description FII USA, Inc., a Foxconn ... Comprehensive benefits package including medical, dental, and vision insurance coverage. * Basic ...

Foxconn WI

Program Manager

Mount Pleasant, WI · On-site

$95 - $135/hr

Program Management Employment Type: Full Time Location: SMC Description FII USA, Inc., a Foxconn ... Comprehensive benefits package including medical, dental, and vision insurance coverage. * Basic ...

Sanmina

Program Manager

Pleasant Prairie, WI · On-site

Program Manager - Pleasant Prairie (Kenosha, WI) Sanmina Corporation (Nasdaq: SANM) is a leading ... medical, multimedia, computing and storage, automotive and clean technology sectors. Sanmina ...

Foxconn WI

Program Manager

Mount Pleasant, WI · On-site

The Program Manager will serve as the primary point of contact for assigned programs, driving ... Comprehensive benefits package including medical, dental, and vision insurance coverage. * Basic ...

Plexus Corp.

Program Manager

Buffalo Grove, IL · On-site

$93K - $140K/yr

... including medical, dental, and vision insurance, paid time off, retirement savings, and ... The Program Manager leads the tactical interface between the customer and various Plexus functional ...

Plexus Corp.

Program Manager

Buffalo Grove, IL · On-site

$93K - $140K/yr

... including medical, dental, and vision insurance, paid time off, retirement savings, and ... The Program Manager leads the tactical interface between the customer and various Plexus functional ...

Nemera

Head of Program Management

Buffalo Grove, IL · On-site

$145K - $165K/yr

Manage and organize the activity of the Program Management team: planning, organization of work ... Background in medical device,pharmaceutical industry or industries of mass production such as ...

Nemera

Head of Program Management

Buffalo Grove, IL · On-site

$145K - $165K/yr

Manage and organize the activity of the Program Management team: planning, organization of work ... Background in medical device,pharmaceutical industry or industries of mass production such as ...

Nemera

Head of Program Management

Buffalo Grove, IL · On-site

Manage and organize the activity of the Program Management team: planning, organization of work ... Background in medical device,pharmaceutical industry or industries of mass production such as ...

MRINetwork Jobs

Operations Manager

Buffalo Grove, IL · On-site

... medical device components. This position is responsible for managing the overall production function, while collaborating with program management, quality assurance, engineering, maintenance, and ...

MRINetwork Jobs

Operations Manager

Buffalo Grove, IL · On-site

... medical device components. This position is responsible for managing the overall production function, while collaborating with program management, quality assurance, engineering, maintenance, and ...

MRINetwork Jobs

Operations Manager

Buffalo Grove, IL · On-site

... medical device components. This position is responsible for managing the overall production function, while collaborating with program management, quality assurance, engineering, maintenance, and ...

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Showing results 21-40

All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Kenosha, WI

Medical Device Program Manager information

See Kenosha, WI salary details

$37.6K

$104.8K

$153.2K

How much do medical device program manager jobs pay per year?

As of Sep 4, 2026, the average yearly pay for medical device program manager in Kenosha, WI is $104,829.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,600.00 and $129,300.00 per year, depending on experience, location, and employer.

What is a medical device program manager?

A Medical Device Program Manager oversees the planning, development, and execution of projects related to medical devices within a company. They coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and serve as the main point of contact for stakeholders. Their role is crucial in bringing safe and effective medical devices from concept to market, ensuring that all aspects of the program meet quality and regulatory standards. Medical Device Program Managers often work closely with engineering, quality assurance, regulatory affairs, and marketing teams.

How does a medical device program manager typically collaborate with cross-functional teams during product development?

A Medical Device Program Manager works closely with cross-functional teams including engineering, regulatory affairs, quality assurance, manufacturing, and marketing throughout the product development lifecycle. They coordinate timelines, facilitate communication, and resolve conflicts to ensure project milestones are met while maintaining compliance with regulatory standards. Regular meetings and progress updates are essential, as the Program Manager acts as a central point of contact to align various team goals and address issues proactively. This collaborative approach helps streamline development and supports successful product launches.

What are the key skills and qualifications needed to thrive as a medical device program manager, and why are they important?

To thrive as a Medical Device Program Manager, you need a strong background in project management, regulatory compliance, and biomedical engineering or a related field, often supported by a relevant degree and industry experience. Familiarity with project management tools (such as MS Project), quality management systems (QMS), and certifications like PMP or Six Sigma are highly valued. Exceptional leadership, cross-functional communication, and problem-solving skills help drive successful product development and team coordination. These competencies ensure programs meet regulatory standards, stay on schedule, and deliver safe, effective medical devices to market.

What is the difference between Medical Device Program Manager vs Medical Device Quality Engineer?

AspectMedical Device Program ManagerMedical Device Quality Engineer
CredentialsProject management certifications, engineering degreeQuality assurance certifications (e.g., CQE), engineering degree
Work EnvironmentCross-functional teams, project planning, product developmentQuality systems, compliance, testing, and validation
Employer & Industry UsageMedical device companies, manufacturing, R&DRegulatory agencies, manufacturing, quality departments
Search & Comparison IntentManaging projects, product launches, timelinesEnsuring quality, compliance, risk management

The Medical Device Program Manager focuses on overseeing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Engineer concentrates on maintaining quality standards, regulatory compliance, and testing processes. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What are popular job titles related to Medical Device Program Manager jobs in Kenosha, WI?

For Medical Device Program Manager jobs in Kenosha, WI, the most frequently searched job titles are:

What job categories do people searching Medical Device Program Manager jobs in Kenosha, WI look for?

The top searched job categories for Medical Device Program Manager jobs in Kenosha, WI are:

What cities near Kenosha, WI are hiring for Medical Device Program Manager jobs?

Cities near Kenosha, WI with the most Medical Device Program Manager job openings:

Medical Device Program Manager jobs near you
Infographic showing various Medical Device Program Manager job openings in Kenosha, WI as of June 2026, with employment types broken down into 1% As Needed, 78% Full Time, 20% Part Time, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $104,829 per year, or $50.4 per hour.

Program Manager

Nemera

Buffalo Grove, IL • On-site

Full-time

This job post has expired 2 days ago. Applications are no longer accepted.

Nemera rating

8.8

Company rating: 8.8 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

Company Description
With sales of €500m and 2,800 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing.
Nemera's manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon).
We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities.
Job Description
Position Purpose: Program Manager provides successful new and existing product introduction through effective utilization of communication, project coordination and people management skills
KEY RESPONSIBILITIES/ESSENTIAL FUNCTIONS:
  • Utilizes technical experience to validate product tooling and automation design approach.
  • Maintains strong interaction with manufacturing environment to support products and equipment design modifications on existing business.
  • Creates and executes project work plans and revises as appropriate to meet changing needs and requirements.
  • Directs project teams as the main point of contact for suppliers and customers.
  • Manages daily operational aspects of a project, including identification of resources needed and assigning individual responsibilities.
  • Reviews deliverables prepared by team before passing to client.
  • Effectively applies current methodology and enforces project standards by complying with project guidelines and company standards.
  • Partners with the Quality department to prepare for engagement reviews and quality assurance procedures.
  • Manages project budget, analyzes project profitability, revenue, margins, bill rates and utilization.
  • Identifies business development and "add-on" sales opportunities as they relate to a specific project.
  • Holds regular status meetings with project team and communicates relevant project information to management.
  • Provides technical knowledge to customer in support of Sales team.
  • Leads cross functional teams in the development and introduction of new programs into the lean manufacturing environment.
  • Estimates or revises costs on existing or new molding/assembly programs and directs modifications and changes to existing molds from customer revisions.
  • Works with the engineering team to acquire equipment prices for new or revised programs.
  • Communicates effectively with clients to identify needs and evaluate alternative business solutions.
  • Adheres to company safety policies.
  • Other duties as assigned

POSITION REQUIREMENTS:
  • Bachelor's degree in Engineering or related field
  • 5 years' experience in Project Management
  • Understanding and experience with automation in manufacturing industry strongly preferred
  • Understanding of lean and continuous improvement practices
  • Understanding of injection molding, tooling, materials, processing, etc.

PREFERRED KNOWLEDGE/SKILLS:
  • Clear and well organized oral and written communication
  • Be able to motivate others to a common goal
  • Strong computer skills, including Microsoft Office applications

WORK ENVIRONMENT:
  • Works in an office and clean manufacturing environment that may include moderate noise levels and required appropriate PPE and cleanroom apparel
  • Some travel required

ADDITIONAL NOTES
This Job Description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee and may be revised at any time by the Company.
Qualifications
POSITION REQUIREMENTS:
  • Bachelor's degree in Engineering or related field
  • 5 years' experience in Project Management
  • Understanding and experience with Automation in manufacturing industry strongly preferred
  • Understanding of lean and continuous improvement practices
  • Understanding of injection molding, tooling, materials, processing, etc.

PREFERRED KNOWLEDGE/SKILLS:
  • Clear and well organized oral and written communication
  • Be able to motivate others to a common goal
  • Strong computer skills, including Microsoft Office applications

Additional Information
Why Join Nemera?
At Nemera, we prioritize patients when creating drug delivery devices, understanding that accurate dosing and ergonomics are crucial for treatment adherence. Joining Nemera means becoming part of a team that enjoys working together and consistently delivers on its commitments. We take pride in our work because it improves patients' lives.
We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group, if you want to discover more about Nemera, please look at our website www.nemera.net
Know someone at Nemera? We have a Referral Program so, be sure to have them submit you as a referral prior to applying for this position!
POSITION RANGE: $115,000 - $125,000 Salaried(This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.)
For US Benefits, CLICK HERE.
Nemera is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other protected class indication. This company is required by federal law to hire only persons who can establish they are eligible to work in the United States.
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