Minimum of 6 years full-time medical device engineering/quality/regulatory technical experience. This experience shall be in addition to any college internships. Relevant experience in other areas ...

1 Exactech Full Time Jobs Hiring Near You
Minimum of 6 years full-time medical device engineering/quality/regulatory technical experience. This experience shall be in addition to any college internships. Relevant experience in other areas ...
Exactech Jobs Information
Do workers at Exactech get paid breaks?
40% of people say they don’t get paid breaks.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and March 2026.
Does Exactech pay people when they’re sick?
40% of people say they wouldn’t get paid if they were sick but scheduled to work.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and August 2025.
Do Exactech workers get to choose the shifts they work?
60% report that they don’t have enough control over which shifts they work.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and August 2025.
How easy is it to get time off at Exactech?
67% of people report it’s easy to get time off.
Based on data from 6 people who took the Breakroom Quiz between February 2025 and March 2026.
Do Exactech managers change schedules at the last minute?
100% of people say their manager doesn’t change their shift schedule at the last minute.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and August 2025.
Do jobs at Exactech spill into time workers aren’t paid for?
20% of people report that their job takes up time that they don’t get paid for.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and August 2025.
How easy is it to take sick days at Exactech?
67% of people report that it’s hard to take time off if they are sick.
Based on data from 6 people who took the Breakroom Quiz between February 2025 and March 2026.
Do people at Exactech feel treated with respect by their managers?
60% of people say they’re not treated with respect by their managers.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and March 2026.
Is it stressful to work at Exactech?
67% of people say they often feel stressed at work.
Based on data from 6 people who took the Breakroom Quiz between February 2025 and March 2026.
Do people at Exactech enjoy their jobs?
50% of people report they don’t enjoy their job.
Based on data from 6 people who took the Breakroom Quiz between February 2025 and March 2026.
Do people at Exactech recommend working with their team?
67% of people report that they wouldn’t recommend working with their immediate team to a friend.
Based on data from 6 people who took the Breakroom Quiz between February 2025 and March 2026.
Do people get enough training when they start at Exactech?
67% of people report they didn’t get enough training when they started working here.
Based on data from 6 people who took the Breakroom Quiz between February 2025 and March 2026.
Do people get support to advance at Exactech?
In the last year, 50% of people report not being given support to advance their career here.
Based on data from 6 people who took the Breakroom Quiz between February 2025 and March 2026.
Do people think Exactech’s headquarters understands what’s happening where they work?
100% of people think that this employer’s headquarters or owners don’t have a good understanding of what’s really happening where they work.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and August 2025.
Do workers feel well informed about how Exactech is doing?
80% of people feel that they aren’t kept well informed about how the company is doing as a whole.
Based on data from 5 people who took the Breakroom Quiz between February 2025 and March 2026.
What are the most popular jobs at Exactech?

Exactech rating
8.0
Based on 6 frontline employees who took The Breakroom Quiz
Job description
- Quality Systems and Regulatory Compliance:
- Know and apply the Quality System and any appropriate Federal and International standards (FDA, ISO 13485, MDSAP, EU MDR, etc.)
- Provide leadership and strategy for the team in the overall administration and maintenance of the QMS processes, ensuring alignment with organizational goals.
- Ensure that Quality Management Systems documentation meets the required guidelines for maintaining FDA compliance and ISO/EC/MDR certification.
- Support the strategic initiatives of the company to achieve and maintain regulatory compliance.
- Corrective and Preventive Action:
- Oversees CAPA system, including maintenance, development and system validation.
- Develops and facilitates continuous training and development for the CAPA process, including root cause analysis and verification of effectiveness.
- Responsible for the reporting of CAPA system KPIs during Quality Systems Governance and Management Review.
- Operates as lead Subject Matter Expert during internal/external audits and inspections..
- Product/Process Nonconformance:
- Oversees NC system, including maintenance, development and system validation.
- Supports cross-functional teams with investigations, root cause analysis, escalation decisions, and dispositions.
- Operates as lead Subject Matter Expert during internal/external audits and inspections.
- Product Corrections and Removals:
- Oversees the process for product event escalations, health hazard evaluation, and execution of product corrections and removals.
- Provides guidance and drives cross-functional collaboration to make timely decisions, based upon product risk.
- Supports cross-functional teams with investigations, root cause analysis, escalation decisions, and final decisions.
- Operates as lead Subject Matter Expert during internal/external audits and inspections.
- Training and Cross-Functional Responsibilities:
- Oversees the Learning Management Solution (LMS), including maintenance, development and system validation.
- Develop training and competency solutions to meet the needs of the company and its Quality Management System.
- Monitors Quality Systems training curricula for completeness, appropriateness and execution.
- Responsible for the reporting of LMS system KPIs during Quality Systems Governance and Management Review.
- Operates as lead Subject Matter Expert during internal/external audits and inspections.
- Data Analytics & Reporting Responsibilities:
- Assist with the development of training materials and documentation to ensure effective dissemination of knowledge to team members and stakeholders.
- Responsible for compiling process data for presentation during Quality Systems Governance and Management Reviews.
- Facilitates Quality Systems Governance and Management Review meetings in accordance with company procedures.
- Bachelor's Degree in Engineering or related science from an accredited institution required; Master's Degree preferred.
- Minimum of 6 years full-time medical device engineering/quality/regulatory technical experience. This experience shall be in addition to any college internships. Relevant experience in other areas may be considered.
- Experience in Change Management documentation systems preferred.
- Experience in electronic Quality Management Systems solutions (e.g. SmartSolve IQVIA, Cornerstone, Teamcenter).
- Experience in data management and reporting utilizing PowerBI.
- Professional Certification through the American Society for Quality (ASQ) or equivalent in Auditing for Medical Devices.
- Experience in software validation, operating within a Quality Management System
- Demonstrated ability to lead cross-functional teams and project
- Demonstrated ability to communicate effectively quality related discussions
- Experience with the development, implementation, and maintenance of electronic solutions for Quality Management Systems elements such as: CAPA, Audits, Data Analysis, etc.
- Demonstrable knowledge of all domestic and international Quality System regulations.