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Medical Device Manufacturing Jobs in Indiana (NOW HIRING)

Understanding of scientific principles and manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and assembly ...

Manufacturing Engineer

Warsaw, IN · On-site

$70K - $90K/yr

Experience in an ISO 13485, ISO 9001, or medical device manufacturing environment preferred * Excellent customer service skills via written and verbal communication required * Strong computer skills ...

Quality Engineer

Noblesville, IN · On-site

$67K - $87K/yr

Within the medical device manufacturing industry is preferred. Level: Engineer II * Bachelor's degree in Engineering or technical field equivalent experience. * 2 - 5 years of experience working in ...

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SUMMARY The Document Control Associate is responsible for maintaining the integrity of the Quality Management System (QMS) in a regulated medical device manufacturing environment. This role ensures ...

Electrical Technician

Warsaw, IN · On-site

$25 - $30/hr

Medical Device Manufacturing Company Duration: 6 Months (Possible Extension) Location: Warsaw, IN 46582 Shift: 1st Shift * Perform electrical installations and repairs. * Troubleshoot electrical ...

Medical Device manufacturing preferred Benefits Include: * Medical, Vision and Dental Insurance * Short-Term Disability * Life Insurance * 401(k) - 50% company match (up to 10% contribution) * Paid ...

Medical Device manufacturing preferred Benefits Include: * Medical, Vision and Dental Insurance * Short-Term Disability * Life Insurance * 401(k) - 50% company match (up to 10% contribution) * Paid ...

Specifically we are seeking people with knowledge of the design and manufacture of IVD cancer and ... Provide Medical Device QMS assessment and device expertise leadership and mentoring in areas of ...

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Specifically we are seeking people with knowledge of the design and manufacture of IVD cancer and ... Provide Medical Device QMS assessment and device expertise leadership and mentoring in areas of ...

New

Showing results 41-60

Medical Device Manufacturing information

See Indiana salary details

$17

$25

$38

How much do medical device manufacturing jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for medical device manufacturing in Indiana is $25.81, according to ZipRecruiter salary data. Most workers in this role earn between $21.97 and $30.19 per hour, depending on experience, location, and employer.

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

To thrive in Medical Device Manufacturing, you need strong attention to detail, knowledge of quality assurance processes, and an understanding of regulatory standards such as ISO 13485 or FDA requirements. Experience with manufacturing equipment, ERP systems, and specialized tools for assembly and testing is typically required, and certification in areas like Six Sigma or Lean Manufacturing can be advantageous. Effective communication, teamwork, and problem-solving skills help individuals excel in fast-paced, multidisciplinary environments. These skills are vital for maintaining product safety, ensuring regulatory compliance, and meeting production targets in the highly regulated medical device industry.

Is medical device manufacturing a good job?

Medical device manufacturing is considered a stable and growing field with opportunities for skilled workers, including roles in assembly, quality control, and engineering. It often requires attention to detail, technical skills, and adherence to safety and regulatory standards, with potential for career advancement and competitive wages.

What career advancement opportunities are available in medical device manufacturing?

Medical Device Manufacturing offers a variety of career advancement paths, allowing employees to move into roles such as production supervisor, quality assurance specialist, or process engineer as they gain experience. Many companies provide on-the-job training, mentorship programs, and support for additional certifications to help employees further develop their technical and leadership skills. Team members who demonstrate strong performance and a commitment to continuous improvement may also transition into management positions or cross-functional roles in research and development, regulatory affairs, or supply chain management. This field values both specialized technical expertise and a proactive approach to professional growth, providing long-term career stability and diverse opportunities.

What is a medical device manufacturing job?

A Medical Device Manufacturing job involves producing, assembling, and testing medical devices to ensure they meet regulatory and quality standards. Workers in this field may operate machinery, inspect products, and follow strict guidelines to maintain safety and efficiency. Roles can range from machine operators and quality control inspectors to engineers and regulatory compliance specialists. This industry is essential for creating devices like surgical instruments, pacemakers, and diagnostic equipment used in healthcare. Attention to detail, adherence to regulations, and technical skills are key for success in this field.

What are popular job titles related to Medical Device Manufacturing jobs in Indiana? For Medical Device Manufacturing jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Medical Device Manufacturing jobs? Cities in Indiana with the most Medical Device Manufacturing job openings:
Infographic showing various Medical Device Manufacturing job openings in Indiana as of August 2026, with employment types broken down into 77% Full Time, 17% Contract, and 6% Nights. Highlights an 100% In-person job distribution, with an average salary of $53,679 per year, or $25.8 per hour.

Full-time

Re-posted 25 days ago


Job description

Working at Freudenberg: We will wow your world!

Responsibilities:
  • Lead development of accuratemanufacturing cost models, make-vs-buy decisions, work-center costs, and support quote generation and pricing strategy for new business or large sustaining initiatives.

  • Establish, track, and report key performance metrics for development, project progression, and launch; champion continuous-improvement and Lean/Six Sigma activities to boost quality, delivery, and cost.

  • Gather and translate user, customer, clinician, and/or market needs and inputs into clear product and business requirements; present data-driven recommendations to stakeholders.

  • Maintain project documentation in line with internal procedures and notified-body expectations, supporting audits and ensuring robust change-control and traceability. Prepare reports and project summaries to communicate the status of projects on a regular basis.

  • Provide technical and project-management leadership, set priorities, allocate tasks, mentor team members, and foster a culture of efficiency, innovation, and regulatory excellence across the organization.

  • Manages a few discrete projects with teams, operating within a defined PDP process delivering to achieve defined scope, schedule, and budget performance goals.

  • Familiarity with and managing efforts for compliance with ISO standards, country-specific (FDA, MDR, Health Canada, PMDA, etc.), GMP regulations, and customer requirements.

  • Input and review for design history files, device master records, risk analyses, and validation protocols/reports (IQ/OQ/PQ) to ensure designs, processes, equipment, and products meet client, regulatory, and business needs.

Qualifications:
  • Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field.

  • 3+ years' experience in Medical Device or related industry

  • 2+ years' experience in leading teams in a manufacturing or engineering environment, with demonstrated experience of managing work within a project plan framework, including managing a schedule, budget, scope, progress, and reporting.

  • Understanding of scientific principles and manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and assembly, including the materials used.

  • Demonstrated experience with formal problem-solving methodologies, critical thinking, and deductive skills.

  • Understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971, and 45001. Knowledge of GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements (i.e., 21 CFR 820 in the United States, and EU MDR).

  • Demonstrated experience using Lean/Six Sigma tools as necessary for new and continuous improvement projects.

  • Demonstrated experience providing leadership and managing multiple projects of low to medium complexity.

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Freudenberg Medical LLC