Careers

At Avation Medical, we are seeking candidates who are driven by the desire to bring innovative medical technologies to market.

Candidates that are intellectually curious, motivated by cutting edge technology, and energized by working with a diverse team of professionals are strongly encouraged to apply.

Considered applicants must be:

  • Self-empowered leaders who take individual ownership.
  • Energetic and enjoy working in a fast-paced environment.
  • Open to new ideas and view-points in a team environment.

job postings

seeking exceptional candidates who are determined to make a difference

Manufacturing Operations Manager

Columbus, OH – Headquarters

Apply your creativity and passion to develop innovative medical devices that can greatly improve patients' lives. We take pride in a truly entrepreneurial environment, unique technical challenges and a collaborative culture. We welcome you to explore Avation and be part of a talented team and an exciting company.

Key Responsibilities
  • Plan, execute and lead manufacturing operations for new medical device systems
  • Manage and train manufacturing operators, technicians and inspectors
  • Set up production line, equipment and develop manufacturing processes
  • Define yield targets, create process FMEA and statistical process controls
  • Create manufacturing process documentation including device history records
  • Lead plans for finished goods, system packaging and labeling
  • Facilities Management in compliance with OSHA, cGMP and safety procedures
  • Lead, track and investigate non-conformances, CAPA and production issues
  • Monitor and maintain manufacturing equipment and fixture requirements
  • Plan production, KPI's and inventory schedules based on forecasts
  • Plan and conduct process validation - IQ/OQ/PQ
  • Key part of project teams in transferring designs into scalable manufacturing
Qualifications
  • Bachelor's in Mechanical or Industrial Engineering
  • Minimum 8-12 years of professional experience, including 3 years in medical device manufacturing
  • In-depth knowledge of 21 CFR 820, ISO 13485, GMP and FDA requirements
  • Familiarity with principles of Six Sigma, lean manufacturing
  • Direct experience with packaging and labeling for medical devices
  • Familiarity with electromechanical products, software and medical device development
  • Ability to multi-task and collaborate on cross-functional projects
  • Strong team leadership with ability to enforce discipline and schedules
  • Independent, creative, collaborative with strong positive can-do attitude
Avation Culture

We are seeking candidates who are.:

  • Driven by the desire to bring innovative medical technologies to market that will improve the lives of patients.
  • Passionate about applying themselves to improve the lives of patients.
  • Intellectually curious, motivated by innovation and open to new ideas.
  • Leaders who take individual ownership while placing high value on teams.
  • Energetic and enjoy working in a fast-paced environment.
We are not working with recruiters to fill this position.

Senior Test and Validation Engineer

Valencia, CA – Headquarters

Apply your creativity and passion to develop innovative medical devices that can greatly improve patients' lives. We take pride in a truly entrepreneurial environment, unique technical challenges and a collaborative culture. We welcome you to explore Avation and be part of a talented team and an exciting company.

h5>Key Responsibilities
  • Lead hardware and software validation strategy for medical device systems
  • Plan, conduct and document tests per standards such as IEC60601 and IEC62304
  • Coordinate Verification and Validation tests, author protocols and execute tests
  • Create trace matrix correlating system requirements and validation plans
  • Plan and build necessary setups, equipment, analysis tools and fixtures for testing
  • Develop and validate automated manufacturing tests for systems and sub-systems
  • Create reports, interpret results and provide statistical summaries
  • Analyze system architecture and integration of hardware and software designs
  • Provide timely feedback on issues, risks and system improvements
  • Ensure adherence to design controls and risk management per ISO 14971
  • Work in a cross-functional team and actively contribute to all aspects of the project
Qualifications
  • Bachelor's degree in Electrical, Computer Science or Systems Engineering
  • 5-8 years of experience in medical device product lifecycle development
  • Experience with test planning, execution and protocols in a regulatory environment
  • Knowledge of standards including IEC 60601, IEC 62304, 62366, ISO 14971
  • Hands-on experience with testing/analysis tools such as Matlab, Labview or Python
  • Experience with system integration, architecture, and software-driven medical devices
  • Independent, creative, collaborative with strong positive can-do attitude
Avation Culture

We are seeking candidates who are.:

  • Driven by the desire to bring innovative medical technologies to market that will improve the lives of patients.
  • Passionate about applying themselves to improve the lives of patients.
  • Intellectually curious, motivated by innovation and open to new ideas.
  • Leaders who take individual ownership while placing high value on teams.
  • Energetic and enjoy working in a fast-paced environment.
We are not working with recruiters to fill this position.

Marketing Intern

Columbus, OH – Headquarters

Apply your creativity and passion to develop innovative medical devices that can greatly improve patients' lives. We take pride in a truly entrepreneurial environment, unique technical challenges and a collaborative culture. We welcome you to explore Avation and be part of a talented team and an exciting company.

We are looking for an enthusiastic marketing intern to provide creative ideas to help launch apatient-centric medical device. Intern will help develop and implement marketing strategies.Candidates should be available to work full time between January 2021 and May 2021.

Key Responsibilities
  • Assist in market development activities.
  • Analyze data from market research and clinical studies.
  • Create insightful and directional presentations based on statistical analyses.
  • Develop content and other communications.
  • Support the marketing team in daily administrative tasks.
Qualifications
  • Passion for healthcare marketing and its best practices.
  • Strong analytical and data analysis skills especially statistical analysis.
  • Strong desire to learn and outstanding multi-tasking abilities.
  • Excellent verbal and written communication skills.
  • Skilled in MS Office.
  • Graduate MBA or Undergraduate in Marketing (3rd year +)
Avation Culture

We are seeking candidates who are.:

  • Driven by the desire to bring innovative medical technologies to market that will improve the lives of patients.
  • Passionate about applying themselves to improve the lives of patients.
  • Intellectually curious, motivated by innovation and open to new ideas.
  • Leaders who take individual ownership while placing high value on teams.
  • Energetic and enjoy working in a fast-paced environment.
We are not working with recruiters to fill this position.

Clinical Research Associate/Clinical Monitor

Columbus, OH – Headquarters -

Apply your creativity and passion to develop innovative medical devices that can greatly improve patients' lives. We take pride in a truly entrepreneurial environment, unique technical challenges and a collaborative culture. We welcome you to explore Avation and be part of a talented R&D group and an exciting company.

Key Responsibilities

As a Clinical Research Associate/Clinical Monitor, you will be a part of the Clinical Team and provide support for the execution of our clinical strategy by conducting monitoring activities of assigned clinical trials in compliance with the protocol, ICH-GCP, and all applicable local and federal laws and regulations.:

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; and other duties as assigned.
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites.
  • Evaluating the quality and integrity of site practices-escalating quality issues as appropriate.
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
Requirements
  • Bachelor's Degree in relevant scientific, clinical or engineering discipline.
  • 1 to 3 years of experience as a Clinical Research Associate/Clinical Monitor.
  • Sound knowledge of ICH/GCP and regulatory requirements.
  • Ability to work independently, prioritize actively, seek input, problem solve and work in a team environment.
  • Energy and enthusiasm; candidates should find the work "fun", and have a passion for innovation and in saving and improving lives in neurotechnology.
  • Must possess the initiative to get results, and a "whatever it takes" attitude to do what's necessary to accomplish team objectives with integrity.
  • Proficient working knowledge of MS Word, PowerPoint, Excel and data management software programs.
  • Medical device, neuroscience, start-up experience a plus.
  • Fluent in English, spoken and written
  • Travel up to 70% to support study sites.
Avation Culture

We are seeking candidates who are.:

  • Driven by the desire to bring innovative medical technologies to market that will improve the lives of patients.
  • Passionate about applying themselves to improve the lives of patients.
  • Intellectually curious, motivated by innovation and open to new ideas.
  • Leaders who take individual ownership while placing high value on teams.
  • Energetic and enjoy working in a fast-paced environment.
We are not working with recruiters to fill this position.