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Cmf Designer Jobs in Florida (NOW HIRING)

KLS Martin

Bill Only Specialist I (34660)

Jacksonville, FL · On-site +1

$17.75 - $24/hr

... designed specifically for CMF and cardiothoracic surgeons. KLS Martin is an innovative leader in the treatment of CMF deformities and trauma cases. We use Individual Patient Solutions (IPS) by using ...

KLS Martin

Senior Data Engineer (34454)

Jacksonville, FL · On-site

$97K - $133K/yr

... designed specifically for CMF and cardiothoracic surgeons. KLS Martin is an innovative leader in the treatment of CMF deformities and trauma cases. We use Individual Patient Solutions (IPS) by using ...

KLS MARTIN LP

Sr Analytics Engineer (34453)

Jacksonville, FL

$96K - $132K/yr

... designed specifically for CMF and cardiothoracic surgeons. KLS Martin is an innovative leader in the treatment of CMF deformities and trauma cases. We use Individual Patient Solutions (IPS) by using ...

KLS MARTIN LP

Bill Only Specialist I (34660)

Jacksonville, FL · On-site

$17.75 - $24/hr

... designed specifically for CMF and cardiothoracic surgeons. KLS Martin is an innovative leader in the treatment of CMF deformities and trauma cases. We use Individual Patient Solutions (IPS) by using ...

KLS MARTIN LP

Senior Data Engineer (34454)

Jacksonville, FL

$97K - $133K/yr

... designed specifically for CMF and cardiothoracic surgeons. KLS Martin is an innovative leader in the treatment of CMF deformities and trauma cases. We use Individual Patient Solutions (IPS) by using ...

KLS Martin

HR Administrative Assistant (34343)

Jacksonville, FL · On-site

$17 - $22.50/hr

... designed specifically for CMF and cardiothoracic surgeons. KLS Martin is an innovative leader in the treatment of CMF deformities and trauma cases. We use Individual Patient Solutions (IPS) by using ...

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Showing results 21-40

All JobsCmf Designer JobsCmf Designer Jobs in Florida

Cmf Designer information

See Florida salary details

$26.5K

$62.1K

$82.2K

How much do cmf designer jobs pay per year?

As of Aug 19, 2026, the average yearly pay for cmf designer in Florida is $62,136.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,300.00 and $81,500.00 per year, depending on experience, location, and employer.

What is a CMF designer?

A CMF (Color, Material, and Finish) Designer is responsible for defining the aesthetic and tactile qualities of a product. They research trends, select materials, develop color palettes, and collaborate with engineers and industrial designers to ensure that design intent aligns with functionality and manufacturing feasibility. CMF Designers play a key role in industries like automotive, consumer electronics, and furniture, shaping how products look and feel to enhance user experience and brand identity.

What kind of teams do CMF designers typically work with, and how do they contribute to the product development process?

CMF Designers regularly collaborate with industrial designers, engineers, marketing teams, and manufacturers throughout the product development lifecycle. Their role is to define and specify the colors, materials, and finishes that will not only enhance the visual and tactile appeal of products but also ensure feasibility for mass production. This collaborative approach helps translate brand identity and trends into tangible product features. CMF Designers provide critical input during prototyping, testing, and final approval stages, ensuring consistency and quality from concept to finished product.

What are the key skills and qualifications needed to thrive in the CMF designer position, and why are they important?

To thrive as a CMF Designer, you need a strong background in industrial design, color theory, materials selection, and finishes, often supported by formal education in design or related fields. Expertise in using CAD software, Adobe Creative Suite, and material libraries is typically required, and familiarity with industry certifications can be advantageous. Creative problem-solving, effective communication, and cross-functional teamwork are vital soft skills for this role. These abilities ensure that CMF Designers can develop innovative, manufacturable designs that meet both aesthetic and functional requirements in product development.

How to get into CMF design?

To become a CMF (Color, Material, Finish) designer, develop a strong understanding of design principles, materials, and manufacturing processes. Gaining experience through a relevant degree such as industrial design or product design, building a portfolio showcasing your work, and learning industry-standard tools like Adobe Creative Suite or CAD software are essential steps.

What does a Cmf Designer do?

A Cmf Designer specializes in developing colors, materials, and finishes for products, ensuring they meet aesthetic and functional requirements. They collaborate with design teams, use tools like CAD software, and stay updated on industry trends to create appealing and practical surface treatments. Their work is essential in industries such as automotive, consumer goods, and furniture design.

What are the most commonly searched types of Cmf Designer jobs in Florida?

The most popular types of Cmf Designer jobs in Florida are:

What are popular job titles related to Cmf Designer jobs in Florida?

For Cmf Designer jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Cmf Designer jobs in Florida look for?

The top searched job categories for Cmf Designer jobs in Florida are:

Cmf Designer jobs near you
Infographic showing various Cmf Designer job openings in Florida as of August 2026, with employment types broken down into 86% Full Time, 8% Part Time, 1% Temporary, and 5% Contract. Highlights an 86% Physical, 6% Hybrid, and 8% Remote job distribution, with an average salary of $62,136 per year, or $29.9 per hour.

Preclinical V&V Specialist (34669)

KLS Martin

Jacksonville, FL • On-site, Remote

Full-time

Posted 26 days ago

KLS Martin rating

9.1

Company rating: 9.1 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

Job description

Who We Are
At KLS Martin, we offer a unique opportunity to contribute to the success of a dynamic and thriving company whose products are used daily across the world to help surgical patients.
The KLS Martin Group is a worldwide leader in creating surgical solutions for the craniomaxillofacial and cardiothoracic fields. Surgical innovation is our passion, and we are constantly working with surgeons to improve surgical care for their patients. Our product portfolio includes titanium and resorbable implants for reconstruction, innovative distraction devices to stimulate bone lengthening, over 4,000 surgical instruments, and other surgical products designed specifically for CMF and cardiothoracic surgeons.
KLS Martin is an innovative leader in the treatment of CMF deformities and trauma cases. We use Individual Patient Solutions (IPS) by using our proprietary IPS products where CT scans are used to custom design implants that are created specifically for that individual patient. This technology allows our surgeons to provide the best-in-class treatment for their patients.
KLS Martin Guiding Principles
  • Established, Privately Held Business Group - Responsive to customers, not shareholders. KLS Martin has manufactured medical products since 1896, and we have sold our products in the United States under the KLS name since 1993. We have always been, and always will be, privately owned.
  • Patient Focus - We design products with the patient in mind - CMF, Thoracic & Hand
  • Product to Table - Integrated planning, design, manufacturing and distribution process
  • Educational Partner - Our primary focus for support is on education
  • Inventory Alliance - Inventory management is critical to patient treatment/outcome
  • Surgical Innovation is Our Passion - More than just a tagline

What We Offer
  • We provide full-time employees with a competitive benefits package, including paid parental leave
  • In-house training and professional development opportunities
  • A culture of creativity and innovation by drawing on diverse perspectives and ideas to drive surgical innovation

***LOCAL REMOTE ONLY - Must be within 50 miles of Jacksonville, FL due to occasional in-house meetings ***
Job Summary
The Regulatory V&V Specialist is responsible for assisting completing of verification and validation activities for products in development and review of design & process changes. This role works under the advisement of the Preclinical V&V Manager to ensure that products meet design specifications, regulatory requirements, and user needs prior to clinical trials and market release. The specialist will coordinate cross-functional activities with R&D, Quality Assurance, Regulatory Affairs, and external testing partners to execute robust V&V strategies. Exercises discretion and independent judgement related, but not limited to, domestic and international regulatory submissions and interfacing with regulatory authorities on the submissions.
Essential Functions, Duties, and Responsibilities
  • Assist with the planning, execution, and documentation of V&V activities for medical devices.
  • Develop V&V protocols, test plans, and reports aligned with design control and risk management processes.
  • Collaborate with cross-functional teams to ensure V&V activities are integrated into the product development lifecycle.
  • Ensure compliance with applicable standards (e.g., ISO 10993).
  • Manage external labs and contractors performing biocompatibility, environmental, and performance testing.
  • Support regulatory submissions by providing V&V documentation and addressing regulatory queries.
  • Identify and mitigate risks related to product safety, performance, and usability.
  • Maintain traceability between requirements, testing, and risk analysis documentation.
  • Participate in design reviews and provide feedback on testability and compliance.
  • Support technology transfer from R&D to manufacturing through validated processes.
  • Execution of biological safety evaluations of medical devices according to ISO 10993, including gap assessment activities
  • Ensure compliance to product documentation with respect to Biocompatibility, Manufacturing Processes, Sterilization, Packaging and/or Cleaning Validation information
  • Compile/write/review Biocompatibility Test Plan, Test Report and Risk Assessment of medical devices in accordance with regulatory requirements (ISO, FDA, GLP)
  • Develop Toxicology/Biocompatibility Risk Assessment Strategies and write the Toxicological Risk Assessment report in collaboration with other team members
  • Collaborate with associates of diverse technical backgrounds and partners with Regulatory Affairs, Quality Engineering, Manufacturing, Packaging and Project Teams, to achieve desired project outcomes
  • Coordinator for outsourced studies
  • Continually review the scientific literature to keep current with new technical information
  • Assesses product change requests for impact on biocompatibility impact
  • Builds strategic partnerships to further departmental and organizational objectives
  • Maintains positive and cooperative communications and collaborations
  • Performs other related duties and responsibilities, on occasion, as assigned

Educational and Experience Requirements
  • Minimum educational requirement is a BS degree in relevant scientific disciplines, such as material science, toxicology, chemistry, biology or similar; although comparable areas of study and industry experience is considered for the position
  • 2-4 years experience in the Medical Device Industry
  • Experience in Biocompatibility and familiarity with application of ISO 10993.
  • Experience with FDA Interactions
  • Previous experience leading projects and presenting recommendations based on technical inputs from multiple and varied functions

Knowledge, Skills, and Abilities
  • Maintains high integrity and confidentiality of company and department information
  • Ability to work effectively with all levels of internal and external associates, customers, and colleagues
  • Excellent interpersonal skills with the ability to effectively communicate at all levels internally as well as externally
  • Ability to follow through on issues, make informed decisions that comply with policies and procedures, complete tasks and problem-solve
  • Ability to work with minimal supervision
  • Ability to manage multiple priorities
  • Ability to organize and track multiple projects in a detail-oriented and self-directed manner
  • Ability to work both independently and within a team environment
  • Possess intermediate to advanced level knowledge of Microsoft Office

Skill Requirements
  • Typing/computer keyboard
  • Utilize computer software (specified above)
  • Retrieve and compile information
  • Maintain records/logs
  • Verify data and information
  • Organize and prioritize information/tasks
  • Operate office equipment
  • Verbal communication
  • Written communication
  • Research, analyze and interpret information
  • Investigate, evaluate, recommend action

Physical Requirements
  • Sitting for extended periods
  • Standing for extended periods
  • Extended periods viewing computer screen
  • Walking
  • Reading
  • Speaking
  • Hear/Listen
  • Maintain regular, punctual attendance
  • Writing

Hazards
  • Normal office environment

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
KLS Martin is a drug-free employer

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