Jobs at CONMED Corporation (Now Hiring) — 141 open — Page 4

Design Quality Engineer II

Memphis, Tennessee, United States · On-site

Mid level$1.1B raised

The Design Quality Engineer II is responsible for supporting all quality engineering activities to support the new product life cycle, from concept to commercialization, and sustaining activities. The Design Quality Engi…

Skills: Design Quality Engineering, Risk Management, Design Verification, Design Validation, Complaint Investigation

CONMED Corporation

Warehouse Associate – Quality Control

Atlanta, Georgia, United States · On-site

Entry level$1.1B raised

Job Summary: The Warehouse Associate will be responsible for ensuring the accuracy and quality of inventory, accurate receiving, storing and shipping of products to meet company standards of quality, safety, security, an…

Skills: Quality Control, Inventory Management, Material Handling, Forklift Operation, Pallet Jack Operation

CONMED Corporation

Global Marketing Data Analyst

Largo, Florida, United States · Remote OK

$85k–$148k/yr

Senior$1.1B raised

Are you passionate about turning data into meaningful insights that drive business impact? As a Global Marketing Data Analyst, you’ll play a critical role in helping teams understand what’s working, and what’s next, acro…

Skills: Marketing analytics, Data visualization, Salesforce, Google Analytics, Power BI

CONMED Corporation

Global Website Operations Specialist

Largo, Florida, United States · Remote OK

$75k–$118k/yr

Mid level$1.1B raised

As a Global Website Operations Specialist, you’ll play a critical role in shaping how our brand comes to life online, ensuring our website delivers accurate, compliant, and engaging experiences for audiences around the w…

Skills: Website Operations, Digital Publishing, CMS Management, Web QA, Release Management

CONMED Corporation

Global Website Operations Specialist

Pinellas County, Florida, United States · Remote OK

$75k–$118k/yr

Mid level$1.1B raised

Skills: Website Operations, CMS Management, Web QA, Content Governance, Release Coordination

CONMED Corporation

IT Project Manager

Pinellas County, Florida, United States · Remote OK

$104k–$164k/yr

Senior$1.1B raised

The IT Project Manager ensures successful and timely execution of technical programs across multiple teams in multiple locations and throughout the full system development life cycle working closely with IT and business …

Skills: Project management, Program management, Portfolio management, Agile methodologies, Stakeholder communication

CONMED Corporation

Sales Representative - Advanced Surgical - NYC

New York, New York, United States · On-site

$220k–$270k/yr

Mid level$1.1B raised

CONMED is seeking a Sales Representative to add to our highly talented Advanced Surgical sales force to our NYC team! Here is what we do, how we do it, who you will work with, and our why behind what we do here at CONMED…

Skills: Outside Sales, Medical Device Sales, Relationship Building, Clinical Workflow Knowledge, Presentation Skills

CONMED Corporation

Senior Principal CNC Machinist - 2nd Shift PMO

Largo, Florida, United States · On-site

Mid level$1.1B raised

Duties and Responsibilities: Provide technical leadership to less experienced employees. Act as a first point of contact for Machining Associate, Operators, and Level l Machinists as a Section Leader Train Machining Asso…

Skills: CNC Machining, Mills, Lathes, Swiss Machines, Multi-axis Equipment

CONMED Corporation

Associate Sales Representative - San Jose

Sunnyvale, California, United States · On-site

Mid level$1.1B raised

CONMED is seeking an Associate Sales Representative to add to our highly talented Advanced Surgical sales force in the San Jose, CA region. Here is what we do, how we do it, who you will work with, and our why behind wha…

Skills: Outside Sales, Clinical Sales, Relationship Management, Product Demonstration, Surgical Technology

CONMED Corporation

Sales Representative - Advanced Surgical - Willamette Valley

Eugene, Oregon, United States · On-site

Mid level$1.1B raised

CONMED is seeking a Sales Representative to add to our highly talented Advanced Surgical sales force! Here is what we do, how we do it, who you will work with, and our why behind what we do here at CONMED. What we do: CO…

Skills: Outside Sales, Medical Device Sales, Clinical Knowledge, Relationship Management, Professionalism

CONMED Corporation

Sports Tissue Representative - Orthopedics - Jersey Shore

Atlantic City, New Jersey, United States · On-site

Mid level$1.1B raised

As a Sports Tissue Representative within CONMED Sports Medicine, you will be responsible for driving adoption and accelerating growth of our advanced tissue portfolio, with a primary focus on BioBrace and MTF tissue prod…

Skills: Market Development, Clinical Credibility, Strategic Account Management, Medical Device Sales, Surgeon Relationship Management

CONMED Corporation

Supervisor, Service Operations & Sales Support

Kirkkonummi, Uusimaa, Finland · Hybrid

Senior$1.1B raised

This is a hybrid position, requiring onsite presence at our Clearwater, FL location on Tuesdays, Wednesdays, and Thursdays. Relocation assistance is offered. Position Summary The Supervisor, Service Operations & Sales Su…

Skills: Service operations, Sales support, Team leadership, Contract administration, Inventory management

CONMED Corporation

IT Project Manager

Largo, Florida, United States · Remote OK

$104k–$164k/yr

Senior$1.1B raised

Skills: Project management, Program management, Portfolio management, Agile methodologies, Stakeholder communication

CONMED Corporation

Supervisor, Service Operations & Sales Support

Largo, Florida, United States · Hybrid

Senior$1.1B raised

Skills: Service operations, Sales support, Team leadership, Customer service, Service contract administration

CONMED Corporation

CNC Senior Swiss Machinist - 1st Shift

Largo, Florida, United States · On-site

Mid level$1.1B raised

CNC Senior Machinist - PMO Factory - Focus on Swiss Machines Key Duties and Responsibilities: Operate various advanced CNC machines and assist with set-ups of CNC machines. Primary job function will be the operation of S…

Skills: CNC machining, Swiss machines, Blueprint reading, Mechanical drawings, Precision measurement

CONMED Corporation

Principal HR Business Partner

Utica, New York, United States · On-site

$75k–$118k/yr

Mid level$1.1B raised

CONMED is seeking a strategic and collaborative Principal HR Business Partner at our Utica, N.Y. site to support leaders across our Global Manufacturing Operations organization. In this highly visible role, you'll help d…

Skills: Employee relations, Talent development, Succession planning, Workforce planning, Organizational effectiveness

CONMED Corporation

Demand Planner, Sr Manager - Patient Care & AS

Pinellas County, Florida, United States · Remote OK

Senior+$1.1B raised

The Sr. Demand Planner Manager - Patient Care & Advanced Surgical (AS) serves as a key leader within CONMED’s Integrated Business Planning (IBP) framework, responsible for developing, optimizing, and leading demand plann…

Skills: Demand planning, Forecasting, Integrated business planning, S&OP, Statistical modeling

CONMED Corporation

Sales Representative - Advanced Surgical - Denver, CO

Denver, Colorado, United States · On-site

Mid level$700M raised

Skills: Outside Sales, Medical Device Sales, Relationship Building, Clinical Workflow Knowledge, Presentation Skills

CONMED Corporation

Returned Good Associate I - 1st Shift

Largo, Florida, United States · On-site

Entry level$700M raised

Purpose: This first shift (7am-3:30pm) position is responsible for the receiving and disposition of all product returned for credit, service/repair, loaner pool, rental etc. as assigned within the Returned Goods (RG) Dep…

Skills: Data Entry, Warehousing, Material Handling, Inventory Management, Shipping And Receiving

CONMED Corporation

Mechanical Engineer III - Advanced Surgical

Denver, Colorado, United States · On-site

$82k–$125k/yr

Senior$700M raised

Growth is our focus at CONMED, and we know that innovation is key to growth and our success! We are dedicated to innovation across our product portfolio and believe in the power of engaged talent on our teams. If you hav…

Skills: Mechanical Engineering, 3-D CAD, SolidWorks, Design Controls, ISO 13485

Key Duties and Responsibilities

Supports and provides direction to product development teams for the required quality deliverables.

Ensures that product design meets customer expectations, regulatory requirements, appropriate voluntary standards, and all corporate requirements. Shows focus toward continuous improvement.

Review, assess, and approve product design documentation to ensure compliance throughout product development cycle. Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.

Troubleshoot and direct the resolution of quality issues by fostering effective interdepartmental and cross-functional partnerships.

A relentless focus on the safety and the efficacy of the medical device.

Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.

Review and approve design verification and design validation protocols and reports. Ensure design activities prove design inputs and user needs are adequately addressed.

Leads and provides support on risk management activities with a focus on clinician and patient safety.

Support product development through capability assessment, analyzing performance data, facilitating problem-solving activities, developing quality tools, and quality techniques.

Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.

Review and approve design verification and design validation protocols and reports. Ensure design activities prove design inputs and user needs are adequately addressed.

Leads and provides support on risk management activities with a focus on clinician and patient safety.

Support product development through capability assessment, analyzing performance data, facilitating problem-solving activities, developing quality tools, and quality techniques.

Support sustaining activities such as complaint investigation and complaint trending. Monitor and analyze manufacturing and service trends. Perform Predicate Device reviews and surveillance reports. Able to perform data mining, analyze data and create trend reports.

Demonstrate quality assertiveness and be able to represent the Quality function in various roles such as product support and lifecycle management.

Investigates process and product issues identified through complaints and trend analysis of other conformance data. Works with other functional groups to resolve difficult quality problems on products, processes, or materials used in manufacturing operations.

Direct and facilitate investigations and the corresponding preventative actions and corrective actions that result from abnormal results, customer complaints, quality inquiries, and other quality performance indicators.

Travel Requirements (including international): 0-5%

Support internal and external audits. Provide support for audit preparation activities. Participate in the back-room as needed.

Preferred Requirements

Must be able to interpret and apply Quality Systems Regulations and ISO quality requirements and stay abreast of new industry standards and concepts.

Knowledge of design controls, 21 CFR 820, ISO 13485, ISO 14971, EU MDR, and applicable medical device regulations.

Must be capable to plan schedules and to manage multiple projects simultaneously.

Professional certifications (CQE, CQA, CMQ/OE, Lead Auditor) are desirable.

Design for Six Sigma training is desired along with knowledge of statistical methodologies.

Involvement in back-room support process during external audits and/or inspections.

Experience reviewing design verification and design validation protocols.

Excellent communication, problem solving, organizational, and interpersonal skills are required.

Strong technical writing skills.

Works independently with minimal direction or supervision.

Decision intelligence.

Physical Requirements

Ability to sit/stand for 8 hours.
Ability to sit at a computer terminal for an extended period.

ADA Disclosure:

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.

This position is not eligible for employer based sponsorship.

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.

Jobs at CONMED Corporation (Now Hiring) — 141 open — Page 4

Design Quality Engineer II

Warehouse Associate – Quality Control

Global Marketing Data Analyst

Global Website Operations Specialist

Global Website Operations Specialist

IT Project Manager

Sales Representative - Advanced Surgical - NYC

Senior Principal CNC Machinist - 2nd Shift PMO

Associate Sales Representative - San Jose

Sales Representative - Advanced Surgical - Willamette Valley

Sports Tissue Representative - Orthopedics - Jersey Shore

Supervisor, Service Operations & Sales Support

IT Project Manager

Supervisor, Service Operations & Sales Support

CNC Senior Swiss Machinist - 1st Shift

Principal HR Business Partner

Demand Planner, Sr Manager - Patient Care & AS

Sales Representative - Advanced Surgical - Denver, CO

Returned Good Associate I - 1st Shift

Mechanical Engineer III - Advanced Surgical

Design Quality Engineer II

Tired of cold applications?

Responsibilities

Requirements

Full job description

This is an on-site role in Memphis, TN.

Key Duties and Responsibilities

Supports and provides direction to product development teams for the required quality deliverables.

Ensures that product design meets customer expectations, regulatory requirements, appropriate voluntary standards, and all corporate requirements. Shows focus toward continuous improvement.

Troubleshoot and direct the resolution of quality issues by fostering effective interdepartmental and cross-functional partnerships.

A relentless focus on the safety and the efficacy of the medical device.

Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.

Review and approve design verification and design validation protocols and reports. Ensure design activities prove design inputs and user needs are adequately addressed.

Leads and provides support on risk management activities with a focus on clinician and patient safety.

Support product development through capability assessment, analyzing performance data, facilitating problem-solving activities, developing quality tools, and quality techniques.

Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.

Review and approve design verification and design validation protocols and reports. Ensure design activities prove design inputs and user needs are adequately addressed.

Leads and provides support on risk management activities with a focus on clinician and patient safety.

Support product development through capability assessment, analyzing performance data, facilitating problem-solving activities, developing quality tools, and quality techniques.

Support sustaining activities such as complaint investigation and complaint trending. Monitor and analyze manufacturing and service trends. Perform Predicate Device reviews and surveillance reports. Able to perform data mining, analyze data and create trend reports.

Demonstrate quality assertiveness and be able to represent the Quality function in various roles such as product support and lifecycle management.

Investigates process and product issues identified through complaints and trend analysis of other conformance data. Works with other functional groups to resolve difficult quality problems on products, processes, or materials used in manufacturing operations.

Direct and facilitate investigations and the corresponding preventative actions and corrective actions that result from abnormal results, customer complaints, quality inquiries, and other quality performance indicators.

Travel Requirements (including international): 0-5%

Support internal and external audits. Provide support for audit preparation activities. Participate in the back-room as needed.

Minimum Requirements

B.S. degree in Engineering such as Electrical, Mechanical, or Biomedical Engineering and 2+ years of medical device experience (or equivalent work experience), or M.S. and 1+ years of medical device experience.

Preferred Requirements

Must be able to interpret and apply Quality Systems Regulations and ISO quality requirements and stay abreast of new industry standards and concepts.

Knowledge of design controls, 21 CFR 820, ISO 13485, ISO 14971, EU MDR, and applicable medical device regulations.

Must be capable to plan schedules and to manage multiple projects simultaneously.

Professional certifications (CQE, CQA, CMQ/OE, Lead Auditor) are desirable.

Design for Six Sigma training is desired along with knowledge of statistical methodologies.

Involvement in back-room support process during external audits and/or inspections.

Experience reviewing design verification and design validation protocols.

Excellent communication, problem solving, organizational, and interpersonal skills are required.

Strong technical writing skills.

Works independently with minimal direction or supervision.

Decision intelligence.

Physical Requirements

Ability to sit/stand for 8 hours.

Ability to sit at a computer terminal for an extended period.

ADA Disclosure:

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.

Benefits:

Related keywords

About CONMED Corporation

About CONMED Corporation

Similar companies hiring

Tools

Explore

Platform

Clera

Tools

Explore

Platform

Clera