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Quality Manager Medical Device Jobs in Indiana (NOW HIRING)

Post Market Quality Engineer

Warsaw, IN ยท On-site

$69K - $89K/yr

The Post Market Quality Engineer is responsible for medical device complaint investigations and ... Comply with Quality Management's guidance and instruction and provide complaint status updates.

Comprehensive benefit offerings including medical, dental, vision, 401k with employer match ... The Quality Manager is responsible for overseeing and managing all aspects of quality assurance ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

Competitive salary and comprehensive benefits including medical, dental, vision, life insurance ... What You Will Do as the Quality Manager * Lead all Plant Quality and Food Safety programs ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

Additionally, the specialist must align tasks with a medical quality management system and have experience with healthcare and medical device regulatory, privacy, and risk management requirements.

Competitive salary and comprehensive benefits including medical, dental, vision, life insurance ... What You Will Do as the Quality Manager * Lead all Plant Quality and Food Safety programs ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

The Role We Want You For The Quality Manager will implement, oversee, and manage all aspects of the ... Medical, dental, and vision plans, 401(k), Generous PTO and paid company holidays, Employee ...

Showing results 41-60

Quality Manager Medical Device information

See Indiana salary details

$22.8K

$82K

$150.3K

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

As of Aug 10, 2026, the average yearly pay for quality manager medical device in Indiana is $81,986.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $129,400.00 per year, depending on experience, location, and employer.

What does a quality manager do in the medical device industry?

A Quality Manager in the medical device industry is responsible for ensuring that products meet all regulatory requirements and quality standards throughout their lifecycle. They develop, implement, and monitor quality management systems, oversee internal and external audits, and work closely with manufacturing, engineering, and regulatory teams to maintain compliance with standards such as ISO 13485 and FDA regulations. Their role is critical to ensuring patient safety and product efficacy by preventing defects and ensuring consistent quality.

What are some common challenges quality managers face when ensuring compliance in the medical device industry?

Quality Managers in the medical device industry often encounter challenges such as keeping up with evolving regulatory requirements (like FDA, ISO 13485, and MDR), coordinating cross-functional teams to maintain strict quality standards, and managing documentation for audits. They must also address nonconformities quickly and implement corrective and preventive actions to avoid product recalls. Effective communication and strong attention to detail are essential for navigating these challenges while maintaining product safety and regulatory compliance.

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

AspectQuality Manager Medical DeviceQuality Engineer Medical Device
Primary FocusOversees quality systems, compliance, and team managementDesigns, develops, and implements quality testing and inspection processes
CertificationsISO 13485, Six Sigma, Lead AuditorISO 13485, Six Sigma, Certified Quality Engineer (CQE)
Work EnvironmentManagement, regulatory compliance, cross-department collaborationProduct testing, process improvement, technical analysis
Industry UsageUsed across organizations to ensure overall quality managementUsed in product development and testing phases

The main difference is that the Quality Manager Medical Device focuses on managing quality systems and compliance at a strategic level, while the Quality Engineer Medical Device concentrates on technical testing and process improvements. Both roles require similar certifications and work within the same industry but serve different functions within quality assurance.

What are the key skills and qualifications needed to thrive as a quality manager in the medical device industry?

To thrive as a Quality Manager in the Medical Device industry, you need a solid background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and process improvement, often supported by a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), risk management tools (like FMEA), and certifications such as ASQ Certified Quality Auditor (CQA) or Six Sigma are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring cross-functional alignment. These skills and qualifications are crucial to ensure product safety, regulatory compliance, and the overall success of medical device manufacturing and delivery.
What are the most commonly searched types of Quality Medical Device jobs in Indiana? The most popular types of Quality Medical Device jobs in Indiana are:
What are popular job titles related to Quality Manager Medical Device jobs in Indiana? For Quality Manager Medical Device jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Quality Manager Medical Device jobs? Cities in Indiana with the most Quality Manager Medical Device job openings:
Infographic showing various Quality Manager Medical Device job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $81,986 per year, or $39.4 per hour.

Post Market Quality Engineer

OrthoPediatrics

Warsaw, IN โ€ข On-site

$69K - $89K/yr

Full-time

Re-posted 6 days ago


Job description

Founded in 2006, OrthoPediatrics is an orthopedic company focused exclusively on advancing the field of pediatric orthopedics. As such it has developed the most comprehensive product offering to the pediatric orthopedic market to improve the lives of children with orthopedic conditions. OrthoPediatrics currently markets 53 products that serve three of the largest categories within the pediatric orthopedic market. This product offering spans trauma and deformity, scoliosis, and sports medicine/other procedures. OrthoPediatrics' global sales organization is focused exclusively on pediatric orthopedics and distributes its products in the United States and over 70 countries outside the United States. For more information, please visit www.orthopediatrics.com.
GENERAL SUMMARY: The Post Market Quality Engineer is responsible for medical device complaint investigations and write-ups as part of the Complaint Handling, Medical Device Reporting and Vigilance Reporting process. This position will ensure timely, accurate, and complete failure investigations, root cause analyses, risk analyses, and other complaint-related tasks are performed and documented for product field failures.
ESSENTIAL FUNCTIONS:
  • Work within cross-functional internal and external teams to investigate device field complaints and provide solutions to resolve complaints in a timely manner.
  • Perform failure analysis of medical devices using various types of test equipment, fixtures, and software tools.
  • Utilize applicable quality tools (Root cause analyses) to ensure timely, accurate, and complete failure investigations of product complaints leading to the root cause and ensure that all activities are documented in the complaint management system.
  • Review internal and external documentation such as device history records, material certifications, inspection reports, and any additional supporting documentation for conformance for complaint investigations.
  • Comply with Quality Management's guidance and instruction and provide complaint status updates.
  • Work with Product Line Engineers to complete post market risk assessments and drive periodic updates to risk management documentation and potentially other documents.
  • Develop, update, and maintain Job Aids and Work Instructions to facilitate and standardize investigation activities.
  • Ability to interface with external auditors.

SUPERVISORY RESPONSIBILITIES:
There are no supervisor responsibilities with this position.
QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. (The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
  • Thorough knowledge of specifications, dimensions, tolerances, and GD&T.
  • Ability to work in a strong team environment and/or independently while being self-motivated and having self-direction.
  • Proficient in the use of statistical applications; must be familiar with the use of SPC.
  • Knowledge on non-destructive testing and measuring techniques.
  • Must have excellent verbal and technical writing skills.
  • Must be analytical and can interpret data.
  • Ability to solve problems.
  • Strong working knowledge of medical device quality system regulations and standards (e.g. 21CFR820, ISO 13485, ISO 14971)
  • ISO 13485 Audit Certification preferred
  • 5 years of Medical Device Quality experience preferred.

EDUCATION AND/OR EXPERIENCE: Requires a bachelor's degree in an Engineering discipline, or equivalent experience in a related quality role. ASQ certification preferred. Must have computer skills; (MS-Excel). Knowledgeable in gauging methods and their applications.
LANGUAGE SKILLS: Ability to read and comprehend instructions, correspondence, and memos. Ability to prepare routine reports and correspondence. Ability to communicate effectively with customers, vendors and other employees of the organization. Requires excellent grammar and spelling.
Mathematical Skills: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
Reasoning Ability: Ability to carry out instructions furnished in written, oral, or diagram form. Ability to use critical thinking to deal with problems involving multiple variables in a variety of situations.
Certificates, Licenses, Registrations: Requires a valid driver's license. ISO 13485 Audit Certification
Other Skills and Abilities: Requires the ability to operate a variety of standard office equipment, such as a computer and keyboard, calculator, fax, photocopier, telephone, cell phone, etc. Requires proficiency with Microsoft Word, Excel, Outlook and PowerPoint.
physical demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
While performing the duties of this job, the employee is regularly required to sit and use hands to finger, handle or feel. The employee is frequently required to climb stairs, talk and hear. The employee is occasionally required to stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and ability to adjust focus.
Work Environment: (The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
The noise level in the work environment is that found in a "normal office environment; noise levels during visits to other locations in the building may be moderate and occasionally loud. The employee will be required to travel 5% of the time.
The above statement reflects the general details necessary to describe the principle functions of the occupation described and shall not be construed as a detailed description of all the work requirements that may be inherent in the occupation.