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    Medical Device Quality Engineer I - Santa Clara, United States - Anatomage

    Anatomage
    Anatomage Santa Clara, United States

    1 month ago

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    Description
    Who is Osteoid?


    Candidates should take the time to read all the elements of this job advert carefully Please make your application promptly.


    Osteoid is creating the next generation of seamless and connected 3D dental imaging software and solutions that help accelerate the path to digital dentistry.

    Proven in over ten years of use by thousands of labs and dental practices, Osteoid's software and hardware tools keep dental practices and labs ahead of the curve and allow dentists to competently diagnose any patient scan in 3D.

    An osteoid is a soft organic element that forms bones in the human body. Just like osteoids in the human body, Osteoid is providing the essential software to dental practice success. Osteoid is a wholly owned dental-focused subsidiary of Anatomage. .

    About the Role

    We are looking for a Quality Engineer or Specialist to join our rapidly expanding team.

    As a member of our Quality & Regulatory team, you'll be responsible for developing and maintaining our quality system for our medical device products.

    Together as a team, you'll help ensure our products are safe and follow global quality standards.

    This position is based in Santa Clara, California.

    What You'll Do

    Help manage, implement, maintain, and improve the quality management system for our medical device products.


    Provide support and guidance for introducing and maintaining medical devices in global markets, which may include duties like documentation, auditing support, risk analysis, complaint investigation and handling, CAPA, regulatory submissions, post-market surveillance, and more.

    Work together with other departments to provide a holistic approach to product development

    Requirements

    Skills and Abilities Required

    Strong analytical and problem-solving skills

    Previous success working in a fast-paced, dynamic and creative environment

    Excellent verbal and written communication skills.

    Self-motivated individual who thrives on doing a job well and has the initiative and drive to excel

    Ability to effectively prioritize, organize, and perform a variety of concurrent tasks

    Team player attitude, eager to be part of an ambitious team

    Great interpersonal skills

    Qualities We Look For

    Experience with Medical Device Software and Hardware

    Experience with QMS/eQMS

    Knowledge of ISO 13485 / MDSAP

    Global regulatory affairs experience (FDA, MDD/CE/MDR, UKCA, etc.)

    Document Control experience

    Proficiency in computer technology and operations

    Ability to work independently and as a team

    Demonstrate attention to detail

    Minimum Education and Experience Required

    Degree in scientific, engineering, or related fields.

    2+ years of experience in a quality engineering, quality specialist, quality assurance, or similar role.

    ASQ certification preferred

    Benefits

    What We Offer

    Health, Dental, and Vision care for you and your family

    401K savings plan with employer matching

    Generous PTO leave and paid holidays

    Casual work culture

    Gym Stipend

    Employee Assistance Plan

    Team bonding activities and more

    Osteoid is an Equal Employment Opportunity Employer. We do not offer H-1B Sponsorships at this time. Local candidates preferred.
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