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Medical Device Innovation Jobs in Indiana (NOW HIRING)

Actalent

Med Device Manufacturing Engineer II

Warsaw, IN

$40 - $48/hr

Maintain strong documentation practices aligned with medical device regulatory standards. Essential ... innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients ...

New

ResMed

Automation Specialist (Onsite)

Indianapolis, IN · On-site

Be part of a global leader in medical device innovation, driving cutting-edge manufacturing solutions that improve lives worldwide. This role offers the opportunity to lead transformative projects ...

Nexxt Spine

CNC Mill Setup/Operator

Noblesville, IN · On-site

$20.75 - $27.50/hr

... medical device industry, dedicated to designing, manufacturing, and distributing an expanding portfolio of innovative spinal implants and instruments. We are committed to a culture of innovation ...

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All JobsMedical Device Innovation JobsMedical Device Innovation Jobs in Indiana

Medical Device Innovation information

See Indiana salary details

$20

$47

$91

How much do medical device innovation jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for medical device innovation in Indiana is $47.42, according to ZipRecruiter salary data. Most workers in this role earn between $33.41 and $56.73 per hour, depending on experience, location, and employer.

What is the difference between Medical Device Innovation vs Medical Device Regulatory Affairs?

AspectMedical Device InnovationMedical Device Regulatory Affairs
Primary FocusDeveloping new medical devices, product design, and technological advancementsEnsuring compliance with regulations, managing submissions, and maintaining approval processes
Required CredentialsEngineering, product development, or biomedical backgroundsRegulatory affairs certifications, healthcare law knowledge
Work EnvironmentResearch labs, product development teams, innovation hubsRegulatory agencies, corporate compliance departments
Industry UsageDesign and create innovative medical devicesNavigate regulatory pathways and ensure legal compliance

Medical Device Innovation focuses on creating and developing new medical devices, emphasizing engineering and product design. In contrast, Medical Device Regulatory Affairs concentrates on ensuring that devices meet legal and safety standards, managing approval processes. Both roles are essential in the medical device industry but serve different functions in bringing a product from concept to market.

What are some common challenges faced by professionals working in Medical Device Innovation, and how can they be addressed?

Professionals in Medical Device Innovation often encounter challenges such as navigating complex regulatory requirements, ensuring cross-functional collaboration, and balancing innovation with patient safety. Staying up-to-date with regulatory changes and fostering open communication among engineering, clinical, and regulatory teams are essential for success. Additionally, adopting agile development methodologies and engaging with end-users early in the design process can help address these challenges and lead to more effective, compliant products.

What is medical device innovation?

Medical device innovation refers to the development and improvement of medical instruments, equipment, and technologies used in healthcare to diagnose, treat, or monitor patients. This process involves research, design, prototyping, regulatory approval, and commercialization of new or enhanced medical devices. The goal is to address unmet medical needs, improve patient outcomes, and increase the efficiency of healthcare delivery. Professionals in this field work closely with clinicians, engineers, and regulatory bodies to ensure devices are safe, effective, and compliant with industry standards.

What are the key skills and qualifications needed to thrive in Medical Device Innovation, and why are they important?

To thrive in Medical Device Innovation, you need a strong background in biomedical engineering or related fields, knowledge of regulatory standards, and experience with product development. Familiarity with CAD software, prototyping tools, and regulatory approval processes such as FDA or CE marking is typically required. Creativity, problem-solving, and effective cross-functional communication are standout soft skills in this role. These competencies are essential for designing safe, effective devices that meet market needs and comply with stringent regulations.
What are popular job titles related to Medical Device Innovation jobs in Indiana? For Medical Device Innovation jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Innovation jobs in Indiana look for? The top searched job categories for Medical Device Innovation jobs in Indiana are:
Medical Device Innovation jobs near you
Infographic showing various Medical Device Innovation job openings in Indiana as of June 2026, with employment types broken down into 5% As Needed, 90% Full Time, 2% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $98,641 per year, or $47.4 per hour.
Medical Device Manufacturing Engineer

Medical Device Manufacturing Engineer

PMC Smart Solutions LLC

Shelbyville, IN • On-site

$69K - $89K/yr

Full-time

Posted 9 days ago

PMC Smart Solutions rating

5.8

Company rating: 5.8 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

68th of 79 rated plastic manufacturers

Job description

Job Type
Full-time
Description
  • Do you enjoy building and optimizing manufacturing processes that support high-quality medical device production?
  • Are you energized by solving engineering challenges while developing innovative manufacturing solutions that improve efficiency and quality?
  • Are you looking to join a growing team in the medical manufacturing industry where innovation, collaboration, and continuous improvement directly impact products that save lives?

If yes, PMC SMART Solutions is the place for you!
Who is PMC SMART Solutions?
PMC, as a globally-recognized, award-winning contract manufacturer, provides life-saving medical devices and safety-enhancing automotive components to a broad base of international, market-leading OEMs and Tier One customers.
PMC offers services from design for manufacturability and program management through injection molding, full assembly, packaging and sterilization management, focusing on precise-tolerance, intricate devices and components. For its medical customers, PMC functions under ISO 13485 certification, FDA registration and operates state-of-the-art, certified Class 8 (100,000) clean rooms.
PMC is a certified Women-Owned Business Enterprise, offering a comprehensive range of services while supporting global OEMs' supplier diversity goals.
What would you look forward to in this role?
  • Developing and optimizing manufacturing processes that ensure efficient, high-quality, and cost-effective production of medical devices.
  • Designing tooling, fixtures, and manufacturing workflows that improve production accuracy, repeatability, and operational efficiency.
  • Leading engineering activities that support successful new product launches from development through full production readiness.
  • Partnering cross-functionally with Quality, Operations, customers, and Engineering teams to solve technical challenges and drive project success.
  • Supporting validation activities and regulatory compliance efforts that ensure manufacturing processes meet strict medical industry standards.
  • Playing a critical role in manufacturing products that directly support life-saving medical applications.

What key responsibilities would you assume in this role?
Device Building & Process Optimization
  • Develop and implement manufacturing processes supporting medical device production, including molding, machining, assembly, and post-processing operations.
  • Design and implement custom assembly fixtures, inspection tooling, and manufacturing solutions that improve production accuracy and efficiency.
  • Optimize production workflows to reduce cycle times, improve product yield, and lower overall manufacturing costs.
  • Analyze production data to identify process improvement opportunities and support cost reduction initiatives.
  • Troubleshoot manufacturing challenges, identify root causes, and implement corrective actions that improve operational performance.
  • Support Lean Manufacturing initiatives focused on improving efficiency, reducing waste, and increasing throughput.
  • Evaluate manufacturability of customer device designs to ensure production readiness and efficient manufacturing execution.
  • Provide technical feedback during design reviews to improve manufacturability, assembly performance, and product quality.

Project Launch Support
  • Lead engineering activities supporting projects from initial development through successful product launch and production readiness.
  • Coordinate cross-functional teams including Quality, Operations, customers, and internal stakeholders to align project deliverables and timelines.
  • Facilitate technical meetings that drive project alignment, resolve challenges, and maintain momentum toward successful launch milestones.
  • Support Sales and business development efforts by assisting with cost estimates, manufacturing quotes, and lead time projections for customer proposals.
  • Partner with internal teams to ensure manufacturing readiness before transitioning products into production.

Quality & Validation
  • Develop and execute validation protocols supporting equipment, manufacturing processes, and test methods.
  • Perform validation activities including Test Method Validation (TMV), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Ensure manufacturing processes comply with FDA regulations and applicable medical device industry standards.
  • Support preparation and maintenance of documentation required for customer regulatory submissions and internal quality systems.
  • Collaborate with Quality and Engineering teams to ensure validated manufacturing processes remain scalable, repeatable, and audit-ready.
  • Support ongoing compliance initiatives that reinforce PMC's commitment to quality, safety, and regulatory excellence.

Who will you work side by side to achieve extraordinary results?
  • Quality, Operations, and Engineering teams focused on successful product development and production execution
  • Cross-functional teams supporting new product launches and manufacturing readiness
  • Customers and project stakeholders collaborating on medical device development and production requirements
  • Internal leadership teams focused on innovation, quality, and operational excellence
  • Manufacturing teams committed to producing life-saving products with precision and consistency

Requirements
What is needed to thrive in this role?
  • Strong manufacturing engineering experience supporting process development, production optimization, and product launch activities.
  • Experience developing manufacturing processes involving molding, machining, assembly, and post-processing operations.
  • Experience designing tooling, fixtures, and manufacturing systems that improve efficiency and product quality.
  • Strong troubleshooting and root cause analysis skills with the ability to solve technical manufacturing challenges quickly and effectively.
  • Experience supporting validation activities including IQ, OQ, PQ, and Test Method Validation (TMV).
  • Familiarity with FDA regulations, medical device manufacturing requirements, and regulated quality systems.
  • Experience supporting new product launches and managing engineering deliverables from development through production.
  • Strong project management and cross-functional collaboration skills with the ability to manage multiple priorities simultaneously.
  • Experience with Lean Manufacturing, process improvement methodologies, and continuous improvement initiatives.
  • Strong communication skills and the ability to work effectively with customers, internal stakeholders, and cross-functional teams.
  • A proactive mindset focused on innovation, quality, accountability, and PMC's mission of manufacturing products that save lives.

Apply