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Local Remote Jobs in Florida (NOW HIRING)

Remote Specialist

Sunrise, FL · Remote

$17.25 - $23/hr

We are seeking a detail-oriented and proactive Remote Specialist to support in-office physician ... or local law. We provide reasonable accommodation to qualified individuals with disabilities and ...

Remote Specialist

Sunrise, FL · On-site +1

$17.25 - $23/hr

We are seeking a detail-oriented and proactive Remote Specialist to support in-office physician ... or local law. We provide reasonable accommodation to qualified individuals with disabilities and ...

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Local Remote information

What is a local remote job?

Local remote jobs are positions that allow employees to work remotely, but within a specific geographic area or region outlined by the employer. This means you can work from home or another location within the designated area, rather than commuting to a central office. Companies may require local remote workers for reasons such as time zone alignment, occasional in-person meetings, or knowledge of the local market. These roles offer flexibility while still maintaining some regional connection. Local remote jobs are common in fields like sales, customer support, and administration.

How does a local remote role typically balance on-site and remote work requirements?

A 'Local Remote' role usually allows employees to work from home most of the time while still requiring periodic visits to a nearby office or client site. This hybrid setup offers flexibility for work-life balance but also ensures strong team collaboration and connection to local operations. Employees may be expected to attend in-person meetings, trainings, or team-building events, so reliable transportation and proximity to the office are important. This structure is ideal for individuals who enjoy remote work but appreciate occasional face-to-face interaction with colleagues.

What are the key skills and qualifications needed to thrive as a remote worker?

To thrive as a Remote Worker, you need strong self-motivation, time management, and relevant job-specific expertise, often supported by experience working independently. Familiarity with collaboration tools such as Slack, Zoom, project management platforms, and sometimes proficiency with cloud-based systems is essential. Excellent communication, adaptability, and problem-solving skills help remote workers stand out by maintaining productivity and teamwork across distances. These skills and qualities are vital for delivering results, staying connected, and overcoming the unique challenges of remote work environments.

What is the difference between Local Remote vs Data Analyst?

AspectLocal RemoteData Analyst
Work EnvironmentCan work from a specific location or remotely, depending on employer policiesTypically involves analyzing data, often in an office or remote setting
Required CredentialsVaries; often includes relevant certifications or degrees, flexible locationUsually requires a degree in data science, statistics, or related field, with certifications beneficial
Industry UsageCommon across many industries, flexible in locationPrimarily in tech, finance, healthcare, and marketing sectors
Search & Comparison IntentPeople compare flexible work options for data-related rolesPeople look for data analysis jobs, often considering remote or local options

In summary, Local Remote jobs for data analysts offer flexibility in work location, with requirements similar to traditional data analysis roles. The main difference lies in the work setting—either working from a specific local site or remotely—while the core skills and industry usage remain consistent.

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

The most popular types of Remote jobs in Florida are:

What are popular job titles related to Local Remote jobs in Florida?

For Local Remote jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Local Remote jobs?

Cities in Florida with the most Local Remote job openings:

Infographic showing various Local Remote job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 26% Part Time, and 4% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Preclinical V&V Specialist (34669)

Jacksonville, FL • On-site, Remote

KLS Martin
Manufacturing • 1 - 5K employees

Full-time

Re-posted 18 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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