Supplier Quality Engineer II at CONMED Corporation

Largo, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

26 Sep, 26

Salary

0.0

Posted On

28 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Supplier Quality Engineering, Root Cause Analysis, Quality Assurance Tools, DMAIC, Statistical Principles, ISO 13485, ISO 14971, QSR, AAMI IEC 62304-2006, Corrective and Preventive Actions, Design Specifications, Manufacturing Process Quality Systems

Industry

Medical Equipment Manufacturing

Description

The Quality Engineer II will provide quality engineering support to all functions for the design, procurement, assembly, test, manufacturing, validation, and distribution of medical devices, processes, and quality systems to ensure that all CONMED products are in full compliance with customer and regulatory requirements. This role will focus on supplier quality engineering activities. Key Duties and Responsibilities: Investigate supplier related process and product issues as assigned by supervisor. Work with other functional groups to resolve difficult quality problems on products, processes, or materials used in manufacturing operations. Plans and performs engineering assignments. Coordinates engineering personnel and the activities of the particular group with the various stages of the overall program. Plans, conducts, and supervises engineering assignments, normally involving several smaller or one major project. Schedules work to meet completion dates and technical specifications. Estimates and coordinates personnel needs assigned to projects. Reviews progress and evaluates results. Review and analyze system and requirements specifications. Review and analyze supplier systems and design specifications. Supports development, implementation and maintenance of design and manufacturing process quality systems. Supports corrective and preventive systems, ensuring investigations through to root cause in accordance with other departments. Consults and provides guidance to Design and Manufacturing Engineers and Procurement Professionals, on the use of Quality Assurance tools, ensuring robust quality systems throughout the lifecycle of a product, from design through sustaining. In addition to the main responsibilities listed above the manager is allowed to use discretion to add further duties and tasks based on the business needs which are not explicitly listed here. Required Experience: Bachelor’s degree in Engineering or related discipline 2 years related experience in quality engineering or related fields Preferred Experience: Fundamental understanding of quality philosophies, principles, systems, and methods. Knowledge of management and planning tools, quality tools, preventive and corrective actions, DMAIC, statistical principles and how to overcome barriers to quality improvements. Knowledge of the QSR, ISO14971, AAMI IEC 62304-2006 and ISO 13485. Certified Quality Engineer and Certified Quality Auditor Expected Travel 0-20% This position is not eligible for employer-visa sponsorship This job posting is anticipated to close on July 6, 2026. We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them. Benefits: CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information. Competitive compensation Excellent healthcare including medical, dental, vision and prescription coverage Short & long term disability plus life insurance -- cost paid fully by CONMED Retirement Savings Plan (401K) -- CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period Employee Stock Purchase Plan -- allows stock purchases at discounted price Tuition assistance for undergraduate and graduate level courses Know someone at CONMED? Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives! CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment. Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at 800-929-7176 option #5. CONMED Corporation is a progressive, global medical device company. Through thoughtful leadership, innovation and team work, we are changing the future of medicine. Our 3,500 employees worldwide make meaningful contributions, positively impact the business, and advance in their careers as our company and product portfolio grows. We are a leader in Orthopedics, General Surgery, Gynecology, Gastroenterology, Pulmonology, and Anesthesiology and our employees enjoy challenging and diverse job opportunities across these varied specializations. We are headquartered in upstate New York with additional domestic facilities in FL, CA, MA, CO, and GA. We have an international presence in more than 20 locations throughout Europe, Australia, Latin America, Asia, North America, and the Middle East.

Responsibilities

Provide quality engineering support for the design, procurement, and manufacturing of medical devices to ensure regulatory compliance. Focus on investigating supplier-related process and product issues and implementing corrective and preventive systems.