
Quality Manager - Suppliers & Incoming Inspection
CONMED Corporation · Largo, FL
- On site
- Full-time
- $120,000 / year
- Largo, FL
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Subject: Interested in the Quality Manager - Suppliers & Incoming Inspection role at CONMED Corporation
Hi Taylor — I came across the Quality Manager - Suppliers & Incoming Inspection opening and wanted to reach out directly. I've spent the last few years doing exactly this kind of work, and CONMED Corporation stood out because…
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Job highlights
- Lead supplier quality and incoming inspection teams.
- Oversee supplier qualification and compliance programs.
- Optimize incoming inspection for efficiency and compliance.
- Ensure supplier understanding of specifications.
- Manage non-conformance and documentation.
About the role
Quality Manager Supplier and Incoming Inspection
Department: Quality Assurance
Reports To: Director, Quality Assurance
Direct Reports: Supplier Quality Engineers and Incoming Inspection Team
Job Level: M3
Job Family Group: OPS-QA/RA
Purpose
The Quality Manager for Suppliers and Incoming Inspection oversees ConMed Largo’s supplier quality program, which encompasses supplier qualification, audit processes and compliance, corrective actions, and continuous improvement initiatives. This role also has ownership of the Incoming Inspection operation where the manager will establish strategies to optimize the incoming inspection program, enhancing operational efficiencies, and establishing key performance indicators (KPIs) that ensure timely flow of compliant parts and components to factories and internal customers. Direct reports to this role are Supplier Quality Engineering Team and the Incoming Inspection Supervisor.
Key Responsibilities
- Leadership & Team Management – Lead Supplier Quality Engineering and Incoming Inspection teams, fostering accountability, customer service and process excellence.
- Regulatory Expertise – Act as SME during regulatory inspections and customer audits for supplier management topics.
- Supplier Conformance – Ensure suppliers understand product design specifications and validate / qualify manufacturing processes to meet established requirements.
- Measurement Systems – Establish and guide accurate measurement methods for both legacy and new components.
- Risk Management – Establish and maintain supplier risk assessment processes and support overall supply chain risk mitigation strategies.
- Process Improvement – Develop and execute projects to enhance incoming inspection processes and supplier audit programs.
- Supplier Oversight – Manage supplier qualification process, changes and performance.
- Cross-Functional Collaboration – Partner with Procurement, R&D, Manufacturing Engineering, and Operations to evaluate/onboard suppliers and resolve product and process challenges.
- Performance & Documentation – Oversee non-conformance resolution (root cause, CAPA, verification), manage supplier quality metrics, and ensure robust documentation/traceability.
- Talent Development – Coach and mentor direct reports, build competencies, ensure efficient team performance and maintain a highly engaged team.
Qualifications
- Bachelor’s degree in engineering, Quality, or a related technical field; master’s degree preferred.
- Minimum of 8 years of experience in supplier quality, quality engineering, or manufacturing in a regulated industry (medical devices strongly preferred).
- Minimum of 2 years of supervisory experience.
Preferred Qualifications
- Deep understanding of supplier management, purchasing controls, and compliance (FDA QSR, ISO 13485, MDSAP).
- Demonstrated proficiency in applying Geometric Dimensioning and Tolerancing (GD&T) principles in engineering and quality assurance context.
- Strong working knowledge of manufacturing methods encompassing molding, turning, boring, drilling, and milling among others.
- Knowledge of material properties and applications across metals, plastics, composites, and other engineering materials.
Training / Skills
- Proven skill in leading teams through ambiguity, ensuring clarity of direction and swift execution under critical scenarios.
- Highly organized with proven time-management skills.
- Strong communication and negotiation skills with suppliers and internal teams.
- Proficiency with electronic Quality Management Systems (eQMS).
No visa sponsorship, relocation assistance considered.
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.
Key skills/competency
- Quality Management
- Supplier Quality
- Incoming Inspection
- Regulatory Compliance
- CAPA
- ISO 13485
- FDA QSR
- GD&T
- Risk Management
- Team Leadership
Skills & topics
- Quality Manager
- Supplier Quality
- Incoming Inspection
- Medical Device Quality
- Quality Assurance
- Regulatory Compliance
- CAPA
- ISO 13485
- FDA QSR
- Team Leadership
- Engineering Management
- Manufacturing Quality
- GD&T
- Risk Management
- Auditing
- Supplier Qualification
- Root Cause Analysis
- eQMS
- CONMED Corporation
- Quality Control
How to get hired
- Tailor your resume: Highlight your experience with supplier quality, incoming inspection, and regulatory compliance in the medical device industry. Quantify achievements where possible.
- Address qualifications directly: Ensure your resume and cover letter clearly demonstrate your Bachelor's degree in a relevant field, 8+ years of experience, and 2+ years of supervisory experience.
- Showcase regulatory expertise: Emphasize your knowledge of FDA QSR, ISO 13485, and MDSAP, as well as GD&T and manufacturing methods.
- Prepare for technical questions: Be ready to discuss your experience with supplier risk assessment, process improvement, and leading teams through ambiguity.
- Network with referrals: If you know someone at CONMED, ask them to submit a referral before you apply to leverage the Employee Referral Program.
Technical preparation
Behavioral questions
Frequently asked questions
- What is the primary focus of the Quality Manager - Suppliers and Incoming Inspection role at CONMED Corporation?
- The Quality Manager - Suppliers and Incoming Inspection at CONMED Corporation is primarily responsible for overseeing the company's supplier quality program and the incoming inspection operations. This includes supplier qualification, audits, compliance, corrective actions, continuous improvement, and optimizing the incoming inspection process to ensure compliant parts flow to manufacturing.
- What are the key qualifications for the Quality Manager - Suppliers and Incoming Inspection position at CONMED Corporation?
- Candidates for the Quality Manager - Suppliers and Incoming Inspection role at CONMED Corporation need a Bachelor's degree in engineering, Quality, or a related technical field, with a Master's degree being preferred. A minimum of 8 years of experience in supplier quality, quality engineering, or manufacturing in a regulated industry (medical devices preferred) and at least 2 years of supervisory experience are required.
- What specific regulatory knowledge is important for this Quality Manager role at CONMED?
- For the Quality Manager role at CONMED, deep understanding of supplier management, purchasing controls, and compliance with FDA QSR, ISO 13485, and MDSAP is highly preferred. This expertise is crucial for regulatory inspections and customer audits.
- What kind of team will the Quality Manager lead at CONMED?
- The Quality Manager at CONMED will lead the Supplier Quality Engineering Team and the Incoming Inspection Supervisor, overseeing their respective teams. This involves fostering accountability, customer service, process excellence, and talent development.
- Does CONMED Corporation offer relocation assistance for this Quality Manager position?
- Yes, the job description mentions that relocation assistance is considered for the Quality Manager - Suppliers and Incoming Inspection position at CONMED Corporation, although visa sponsorship is not offered.
- What manufacturing and material knowledge is beneficial for this role at CONMED?
- For the Quality Manager role at CONMED, strong working knowledge of manufacturing methods such as molding, turning, boring, drilling, and milling is beneficial. Familiarity with material properties and applications across metals, plastics, and composites is also advantageous.
- How does CONMED Corporation support its employees' professional development?
