Treace’s mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers’ expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.
Job DescriptionPOSITION SUMMARY:
The Sr. Quality Systems Specialist (SQSS) is responsible for executing and supporting Quality System requirements in maintaining a compliant Quality System (ISO, FDA 21 CFR 820, etc.). Specifically, this role is responsible for creating procedures, assessing changes to procedures, auditing for compliance to procedures, leading CAPA system activities and recall activities, where required.
PRIMARY DUTIES & RESPONSIBILITIES:
Create and update quality system procedures, including performing biennial reviews to drive continuous improvement, align best practices, procedures and applicable regulations (FDA, ISO, etc.)Administer, provide training and maintain SolidWorks Product Data Management (PDM) system and Arena Product Lifecycle Management (PLM) systemModify Arena PLM configurations to meet evolving business processes, including the creation and management of configuration rules, BOM structure standards, and other system configurationsAdminister, manage templates, and issue envelopes for signature within DocuSign platformAdminister and maintain quality system training (new hire, ongoing, annual, etc.) activities in eLMS (Absorb)Supports standards review process by continuously monitoring regulations and guidance documents for required updatesResponsible for processing quality system, marketing collateral, and product documenting engineering change orders, reviewing for completeness and releasing controlled copies for use.Performs internal quality system audits (for areas independent of responsibilities)Supports quality system documents and records for completeness, scans, organizes, and files electronically and physicallySupport post market surveillance activities, as neededExecutes health hazard evaluations and field action activities with direction from the Recall Coordinator. Identify scope of product holds, perform traceability, and physical quarantine of impacted products.Investigate potential non-conformances and recommend CAPA activity to manager. Support CAPA investigations for root cause determination and action implementation/verification.QualificationsEDUCATION & EXPERIENCE:
Minimum high school diploma or equivalent required. An associate or bachelor’s degree in life sciences is strongly preferred.A minimum of 5+ years’ experience in medical device or pharma quality systems role (e.g. Document Control, Quality Control, Post Market, etc.) is requiredPrior root cause analysis training is preferredQuality system auditor training or certification is preferred (ISO, other)All your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessTreace’s mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers’ expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.
Job DescriptionPOSITION SUMMARY:
The Sr. Quality Assurance Specialist (SQAS) is responsible for executing and supporting Quality System requirements in maintaining a compliant Quality System (ISO, FDA 21 CFR 820, etc.). Specifically, this role is responsible for creating procedures, assessing changes to procedures, auditing for compliance to procedures, leading CAPA system activities and recall activities, where required.
PRIMARY DUTIES & RESPONSIBILITIES:
• Create and update quality system procedures, including leading and performing biennial reviews to drive continuous improvement, align best practices, procedures and applicable regulations (FDA, ISO, etc.)
• Responsible for leading impacts resulting from proposed changes to quality system procedures
• Supports standards review process by continuously monitoring regulations and guidance documents for required updates
• Responsible for processing quality system, marketing collateral, and product documenting engineering change orders, reviewing for completeness and releasing controlled copies for use.
• Leads and performs internal and supplier quality system audits (for areas independent of responsibilities)
• Supports Master Audit Schedule, vendor management and leads onsite/desktop audits, and post market surveillance activities as needed
• Executes health hazard evaluations and field action activities with direction from the Recall Coordinator. Identify scope of product holds, perform traceability, and physical quarantine of impacted products.
• Supports timely execution of Quality Plans, Quality System CAPAs, CAPA trending meetings and management reviews
• Investigate potential non-conformances and recommend CAPA activity to manager. Leads CAPA investigations for root cause determination and action implementation/verification.
• Distribute documents for approval and obtain signatures from team members (DocuSign)
• Supports external (FDA, ISO, etc.) compliance audits as well as schedule and manage internal audits as required to maintain quality compliance
Qualifications• An associate or bachelor’s degree in life sciences is strongly preferred; in lieu of degree, a HS Diploma with 7+ years of quality experience in the medical device or related industry is required.
• A minimum of 5+ years’ experience in medical device or pharma quality systems role (e.g. Document Control, Quality Control, Quality Assurance, etc.) is required
• Prior root cause analysis training is preferred
• Quality system auditor training or certification is preferred (ISO, other)
All your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessTreace’s mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers’ expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.
Job DescriptionTreace Medical is seeking an experienced and results-driven Vice President of Commercial Operations to serve as a key strategic and operational leader within our regulated, fast-paced medical device environment. This individual will take charge of optimizing the performance of our commercial organization by overseeing critical functions such as sales operations, business intelligence, pricing, and forecasting. The VP will play an instrumental role in aligning sales, marketing, and other functions to maximize revenue performance, improve operational efficiency, and enhance the customer experience. Additionally, this role will lead automation and optimization efforts across Treace Medical’s processes and systems.
The VP of Commercial Operations will be accountable for:
Strategic Leadership:
Developing and executing commercial operations strategies that drive revenue growth, operational efficiency, and customer satisfaction.Guiding the organization’s overall data-driven decision-making process by leveraging sales analytics and business intelligence.Partnering with cross-functional teams, including Finance, IT, Marketing, and Strategy, to ensure alignment on forecasting, budgeting, and long-range planning.Team Leadership:
Building and leading high-performing teams across sales operations, business intelligence, and pricing functions.Coaching and mentoring team members to foster professional growth in a dynamic, fast-moving environment.Sales Operations & Analytics:
Overseeing sales operations processes, including pipeline management, territory planning & alignment, forecasting, quota setting, and incentive compensation design.Leading revenue forecasting, sales analytics, and business intelligence efforts to generate actionable insights and support executive decision-making.Designing and managing frameworks for pricing, contracting, and profitability analysis.Reporting & Business Intelligence:
Driving the development of advanced tools for tracking key performance metrics, market trends, and competitive insights.Delivering executive-level scorecards, dashboards, and reports to monitor commercial performance.Ensuring the quality, accuracy, and efficiency of sales forecasting, planning, and budgeting processes.Automation & Optimization:
Implementing tools and technologies to enhance commercial effectiveness, such as CRM platforms, BI dashboards, ERP systems, and sales enablement platforms.Leading continuous improvement initiatives and automation projects in partnership with IT and Strategic Initiatives teams.Process Optimization:
Overseeing the preparation and distribution of detailed monthly sales reports, including customized performance and activity matrices.Managing the annual quota-setting process with equitable assignments, monitoring quota effectiveness, and driving adjustments to meet revenue goals.Proactively recommending revisions to sales processes, reporting tools, and analytical frameworks to maintain competitiveness and operational excellence.Qualifications
All your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessTreace’s mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers’ expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.
Job DescriptionThis role is 20 hours/week and will go to June 2026
POSITION SUMMARY:
The Shipping Coordinator is responsible for supporting our procurement, quality, and customer service activities by diligently executing the TMC shipping process, which ensures that all picking, packing, and shipment of products to vendors and customers is executed accurately and timely. This team member supports receiving inspection and returns processing activities including reviewing manufacturing documentation such as material certificates, post-processing certificates, and inspection data as well as reviewing lot numbers, creating labels, and transferring inventory in the Company’s accounting system.
PRIMARY DUTIES AND RESPONSIBILITIES:
Accurately prepares orders for shipment by picking materials, packing, transacting in the Company’s accounting system, and placing in delivery area for pickupCommunicate status of shipments to requestor in a timely fashionCollaborates with operations and assists with scheduling and prioritizing component shipments to suppliersFollow procedures and work instructions and give feedback for improvementMaintain clean and safe work environment by keeping shelves, storage area, and workstations neat and organizedConduct inventory cycle counts and investigate any variance root causes.Actively participate in continuous improvement activitiesComplete general clerical duties including copying, scanning, and emailingPerforms other duties as assignedQualificationsEDUCATION & EXPERIENCE REQUIREMENTS:
High school diploma is required, an Associate’s degree preferredOne (1) year of shipping & receiving experience is strongly preferredProficiency with MS OfficeExperience with ERP Systems, NetSuite experience preferredPeriodic overtime will be requiredAll your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessAt Treace, we are revolutionizing 3D solutions for the treatment of complex bunion deformities. Our innovative, high-velocity approach enables us to consistently exceed customer expectations, delivering minimally invasive solutions that improve patient outcomes and drive efficiency for healthcare providers. By advancing reproducibility and patient satisfaction, Treace empowers foot and ankle surgeons to achieve better surgical results, reduce healthcare costs, and enhance overall care quality.
If you're seeking an opportunity to grow in your sales career while working with a dynamic and diverse team dedicated to meaningful innovation, Treace could be your next great career destination. Together, let's create something greater than ourselves.
Job DescriptionAs the Product Manager, you will own the strategic and tactical management of the company’s product portfolio, from concept to lifecycle management. This includes leading all upstream and downstream marketing initiatives and activities to meet and exceed financial, marketing, and corporate growth objectives.
You will spearhead the development and commercialization of innovative products, work collaboratively across functional teams, and establish enduring relationships with key opinion leaders in the foot and ankle healthcare field. This role requires a forward-thinker who can effectively bridge strategic planning with tactical execution to deliver impactful results.
Key Responsibilities:
Product Development & Commercialization
Develops comprehensive plans for launching major new products.Drives product commercialization strategies and execution.Collaborates with R&D and surgeon designers for seamless product development.Market Strategy & Analysis
Tracks and analyzes market trends to identify and validate new product opportunities.Develops positioning strategies for new and existing products.Conducts in-depth market research to ensure customer needs are met.Analyzes product performance and recommends discontinuation where needed.Collaboration & Cross-Functional Engagement
Works with R&D, Quality, Regulatory, Legal, Manufacturing, and Operations to define customer-centric product specifications.Contributes to setting research and development priorities.Organizes cross-functional product development meetings to ensure alignment.Marketing & Communication
Manages tradeshows, exhibits, and advertising efforts.Collaborates with creative teams to produce marketing materials.Provides field sales teams with training and marketing support to ensure product success.Customer & Physician Engagement
Develops and maintains strong relationships with key physicians and opinion leaders.Supports the planning and execution of medical education events to enhance product adoption.Profitability & Budget Management- Oversees and develops sales budgets for the product line (both short-term and long-term).Monitors budget performance and ensures profitability through corrective measures as needed.QualificationsBachelor’s degree in Business, Marketing, Engineering, or related fields (MBA is highly desirable).
5+ years of experience in product management, preferably in the medical device or healthcare industry.Demonstrated expertise in product launches, marketing strategies, and customer-driven product development.Proficiency in market research and data analytics tools.A proven ability to integrate strategic planning with tactical execution.A strong capacity to interpret and act on market trends and customer needs.Exceptional collaboration skills with the ability to manage cross-functional teams effectively.Knowledge and experience in clinical marketing, preferably in the foot and ankle space or related healthcare sectors.Analytical acuity to determine product success and support data-driven decision-making.All your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessAt Treace, we are revolutionizing 3D solutions for the treatment of complex bunion deformities. Our innovative, high-velocity approach enables us to consistently exceed customer expectations, delivering minimally invasive solutions that improve patient outcomes and drive efficiency for healthcare providers. By advancing reproducibility and patient satisfaction, Treace empowers foot and ankle surgeons to achieve better surgical results, reduce healthcare costs, and enhance overall care quality.
If you're seeking an opportunity to grow in your career while working with a dynamic and diverse team dedicated to meaningful innovation, Treace could be your next great career destination. Together, let's create something greater than ourselves.
Job DescriptionThe Manufacturing Technician will play a critical role in supporting the production of surgical instruments by setting up, operating, and processing metal and Nylon 3D printed components. The ideal candidate will be skilled in the setup, operation, and maintenance of DMLS metal printers and Nylon 12 printers, as well as proficient in post-processing techniques using hand tools and manual equipment. This role requires attention to detail, a strong understanding of manufacturing processes, and the ability to work collaboratively with engineers to meet production and quality standards.
What you will be responsible for:
Manufactures and finishes parts to support production of medical instruments.Manufactures and finishes parts to support product development.Fabricates and builds mechanisms for surgical instruments.Prepares and post-processes DMLS 3D printed Stainless Steel and Nylon 12 parts.Utilizes a variety of hand tools and shop equipment, including belt sanders, Dremel tools, media blasters, and similar equipment, ensuring prototypes achieve design specifications.Performs dimensional and visual inspections to verify parts meet specifications and are functional.Collaborates with engineers to manufacture parts for production purposes.Follows documented procedures and work instructions, completing all required quality documentation.QualificationsAll your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessAt Treace, we are revolutionizing 3D solutions for the treatment of complex bunion deformities. Our innovative, high-velocity approach enables us to consistently exceed customer expectations, delivering minimally invasive solutions that improve patient outcomes and drive efficiency for healthcare providers. By advancing reproducibility and patient satisfaction, Treace empowers foot and ankle surgeons to achieve better surgical results, reduce healthcare costs, and enhance overall care quality.
If you're seeking an opportunity to grow in your career while working with a dynamic and diverse team dedicated to meaningful innovation, Treace could be your next great career destination. Together, let's create something greater than ourselves.
Job DescriptionAre you passionate about quality, precision, and patient safety? Do you thrive in a fast-paced environment where attention to detail is critical? Join our dedicated team as a Senior Quality Control (QC) Inspector and play a pivotal role in ensuring the highest standards within our additive manufacturing operations and state-of-the-art Class 8 cleanroom.
This is an exciting opportunity for a detail-oriented individual who is committed to excellence and eager to make a meaningful impact in a rapidly growing organization.
About the Role:
As a Sr. Quality Control Inspector, you will ensure that our operations align with current Good Manufacturing Practices (cGMP), consistently maintaining the quality and safety of our processes and products. Working cross-functionally, you will interact with multiple teams and levels of the business, contributing to continuous improvement and operational success.
The ideal candidate is a problem solver with a passion for quality and patient safety, and someone who thrives in cleanroom environments and highly regulated industries.
Your key responsibilities will include:
Performing inspections of work-in-progress, finished parts, assemblies, and kits, as well as completing all necessary paperwork for product release.Assembling non-sterile products into kits for final release to the field.Conducting visual and dimensional inspections to ensure compliance with quality specifications.Reviewing device history records to confirm accuracy and completeness.Identifying and documenting product nonconformances, collaborating with Operations for resolution.Participating in the development of future inspection procedures.Setting up, calibrating, and maintaining inspection equipment.Monitoring and maintaining the Class 8 cleanroom environment to ensure alignment with stringent quality and cGMP standards.Adhering to and promoting safety protocols while actively contributing to process improvement efforts.Following aseptic techniques consistently to maintain the integrity of the cleanroom.Collaborating with the Clean Room Team Lead and other team members to ensure seamless communication and operations.Assisting with scheduled cleanroom facility cleaning to uphold a contaminant-free environment.Providing feedback and suggestions for improving QC and manufacturing processes.QualificationsAll your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessAt Treace, we are revolutionizing 3D solutions for the treatment of complex bunion deformities. Our innovative, high-velocity approach enables us to consistently exceed customer expectations, delivering minimally invasive solutions that improve patient outcomes and drive efficiency for healthcare providers. By advancing reproducibility and patient satisfaction, Treace empowers foot and ankle surgeons to achieve better surgical results, reduce healthcare costs, and enhance overall care quality.
If you're seeking an opportunity to grow in your career while working with a dynamic and diverse team dedicated to meaningful innovation, Treace could be your next great career destination. Together, let's create something greater than ourselves.
Job DescriptionThe Prototype Shop Technician plays a key role in supporting the fast-paced iterative development of surgical instruments and implants. This role is responsible for processing metal 3D prints, including machine preparation, post-processing, and finishing prototype components. The technician will work collaboratively with engineers and other machinists to manufacture, assemble, and refine prototype mechanisms. This position involves operating, setting up, and maintaining DMLS metal printers, as well as using hand tools and manual toolroom equipment. The Prototype Shop Technician reports to the Prototype Shop Supervisor.
What you will be responsible for:
Manufacture and finish prototypes in support of product development.Fabricate and build prototype mechanisms for surgical instruments and implant evaluation.Prepare and post-process DMLS 3D-printed parts to meet design requirements.Operate tools and shop equipment, including belt sanders, bandsaws, and grinders.Ensure prototypes align with design intent and engineering specifications.Collaborate with engineers to test and evaluate prototypes.Maintain quality standards and adhere to safety protocols.QualificationsAll your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessTreace’s mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers’ expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.
Job DescriptionThe Receiving Inspection Associate is a critical member of our Operations team, responsible for supporting procurement, quality, and customer service activities. This role ensures all incoming inventory meets the company’s manufacturing and quality standards while adhering to FDA guidelines for the medical device industry. The associate will carry out detailed inspections, verify documentation, and maintain accurate input within the company’s ERP system, contributing to our mission of upholding stringent quality requirements.
In this role, you will:
Thoroughly review all manufacturing documentation (e.g., material certificates, post-processing certificates, inspection data) to verify compliance with quality standards.Perform detailed inspections of incoming components, labels, packaging, and finished goods to ensure they meet the requirements of a medical device company.Identify product non-conformances and take appropriate steps to resolve them.Accurately inspect mechanical parts using microscopes, surface plate setups, and tools such as micrometers, calipers, and bore gauges.Collaborate with suppliers to obtain necessary information or resolve issues.Review lot numbers, create inventory labels, and input data into the company’s ERP system.Assist in scheduling shipments of components to suppliers and finished goods to customers.Follow documented procedures and provide feedback to help improve processes.Qualifications
All your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read LessTreace’s mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers’ expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.
Job DescriptionThis role will be 30 hours/week through the end of March 2026.
The Receiving Inspection Associate is a critical member of our Operations team, responsible for supporting procurement, quality, and customer service activities. This role ensures all incoming inventory meets the company’s manufacturing and quality standards while adhering to FDA guidelines for the medical device industry. The associate will carry out detailed inspections, verify documentation, and maintain accurate input within the company’s ERP system, contributing to our mission of upholding stringent quality requirements.
In this role, you will:
Thoroughly review all manufacturing documentation (e.g., material certificates, post-processing certificates, inspection data) to verify compliance with quality standards.Perform detailed inspections of incoming components, labels, packaging, and finished goods to ensure they meet the requirements of a medical device company.Identify product non-conformances and take appropriate steps to resolve them.Accurately inspect mechanical parts using microscopes, surface plate setups, and tools such as micrometers, calipers, and bore gauges.Collaborate with suppliers to obtain necessary information or resolve issues.Review lot numbers, create inventory labels, and input data into the company’s ERP system.Assist in scheduling shipments of components to suppliers and finished goods to customers.Follow documented procedures and provide feedback to help improve processes.Qualifications
All your information will be kept confidential according to EEO guidelines.
Treace's Privacy Policy
It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
Treace is a drug free employer.
Read Less