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Future Motion Jobs in Colorado (NOW HIRING)

Brains and Motion Education

Warehouse Worker

Denver, CO · On-site

$19.50/hr

If you're ready to make a meaningful impact, consider joining us in shaping the future of learning. Apply today! As a Warehouse Worker at Brains & Motion Education, you will play a crucial role in ...

BRAINS AND MOTION EDUCATION

Warehouse Worker

Denver, CO · On-site

$19.50/hr

If you're ready to make a meaningful impact, consider joining us in shaping the future of learning. Apply today! As a Warehouse Worker at Brains & Motion Education, you will play a crucial role in ...

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Future Motion information

What is the difference between Future Motion vs Electric Skateboard Designer?

AspectFuture MotionElectric Skateboard Designer
CredentialsTypically requires engineering or industrial design background, certifications varyRequires design, engineering, or product development experience, often with portfolio
Work EnvironmentDesign and engineering teams, R&D labs, manufacturing facilitiesDesign studios, R&D departments, collaborative team settings
Industry UsageFocuses on developing and manufacturing electric skateboards and related productsInvolved in designing electric skateboards, focusing on aesthetics and functionality

Future Motion is a company specializing in electric skateboard manufacturing, while Electric Skateboard Designer is a role focused on creating the design and user experience of these products. The former involves product development and engineering, whereas the latter emphasizes design and aesthetics. Both roles often require similar credentials and work in related environments, but their focus areas differ within the industry.

What are popular job titles related to Future Motion jobs in Colorado?

For Future Motion jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Future Motion jobs in Colorado look for?

The top searched job categories for Future Motion jobs in Colorado are:

Future Motion jobs near you
Infographic showing various Future Motion job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, and 3% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Regulatory Affairs Specialist

Synergy Spine Solutions Inc.

Louisville, CO • On-site

$85 - $120/hr

Other

Posted 3 days ago

New

Key responsibilities

  • Maintain and support U.S. regulatory approval for the Synergy Disc, including post-approval requirements, reports, and supplements.

  • Manage and expand international device registrations by preparing technical documentation and coordinating with local representatives.

  • Support regulatory submissions, technical documentation, and assess the regulatory impact of design, labeling, and manufacturing changes.

Job description

Workplace:On-site
Career Type:Full-time
Reports to:Vice President, Regulatory Affairs & Quality Assurance

ABOUT SYNERGY SPINE SOLUTIONS

Synergy Spine Solutions is a medical device company focused on improving the quality of life for patients undergoing spine surgery. We develop motion-preserving technologies that treat degenerative disc disease while supporting the spine’s natural curvature. Our flagship product, the FDA-approved Synergy Disc®, is the first and only artificial cervical disc designed to improve sagittal alignment through a built-in 6-degree lordotic core while delivering intentional motion preservation using time-tested, trusted materials. The Synergy Disc is commercially available in the United States, Europe, Australia, Canada (SAP), South Africa, and Malaysia.

ABOUT THE ROLE

We’re seeking a mid-level Regulatory Affairs Specialist to support the global regulatory lifecycle of the Synergy Disc and future motion-preservation technologies. Working on-site in Louisville, CO, you’ll maintain and expand our regulatory approvals across multiple international markets, manage post-approval obligations for a Class III cervical disc andsupportinginstrumentation. Serve as the regulatory connective tissue between R&D, Quality, Clinical, and our commercial and distributor teams. This is a hands-on role with broad ownership and direct visibility across a focused, fast-moving organization.

KEY RESPONSIBILITIES

  • Maintain and support U.S. regulatory approval for the Synergy Disc, including PMA post-approval requirements, annual reports, and supplements for device, labeling, or manufacturing changes.
  • Manage and expand international registrations across current and new markets (EU, Australia, Canada, South Africa, Malaysia, and others), preparing technical documentation and coordinating with in-country representatives and distributors.
  • Support in authoring, compiling, and maintaining regulatory submissions and technical documentation, including device descriptions, risk documentation, and change assessments.
  • Assess the regulatory impact of design, labeling, materials, and manufacturing changes, and determine submission strategy and requirements across jurisdictions.
  • Support regulatory bodies, including FDA and international regulatory bodies, authorized reps, including responses to deficiencies and information requests.
  • Maintain regulatory records, technical files, registrations, device listings, and establishment registration.
  • Review labeling, packaging, surgeon-facing materials, and marketing/promotional content for regulatory compliance across markets.
  • Partner with Clinical to support ongoing study and post-market data requirements stemming from the IDE/PMA pathway and international clinical trials.
  • Monitor evolving FDA regulations, EU MDR requirements, and international standards relevant to cervical arthroplasty and Class III implants, communicating impact to the organization.
  • Support internal and external audits and regulatory inspections.

QUALIFICATIONS

  • Bachelor’s degree in a life science, engineering, or related technical field.
  • 3–7 years of regulatory affairs experience in the medical device industry; spinal, orthopedic, or implantable (Class III) device experience strongly preferred.
  • Hands-on experience with FDA submissions; PMA and post-approval experience highly desirable (experience with 510(k) and IDE pathways a plus).
  • Experience with international device registrations and familiarity with EU MDR technical documentation.
  • Working knowledge of 21 CFR Part 814 (PMA), 21 CFR Part 820/QMSR, ISO 13485, and ISO 14971 risk management.
  • Strong technical writing skills and meticulous attention to detail.
  • Ability to manage multiple submissions and markets independently in a lean, fast-paced environment.
  • RAC certification a plus but not required.
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