Demo

Staff Compliance Engineer

Katalyst Healthcares & Life Sciences
San Diego, CA Full Time
POSTED ON 3/3/2025
AVAILABLE BEFORE 6/2/2025

Job Description

Job Description

Responsibilities :

  • Expert in IEC 60601-1, IEC 60601-1-6, IEC 60601-1-8, and IEC 60601-1-2, ISO 14971 and experience with particular standards related to infusion pumps (IEC 60601-2-24).
  • Expert in developing strategies according to business per applicable standards encompassing EMC and Safety.
  • Expert in Electrical design review including deep understanding on layouts and schematics (EIT or PE preferred).
  • Able to train cross functional staff on various standards and perform impact assessment on standard updates.
  • Read, interpret and communicate changes in technical regulations, directives and standards.
  • Review new and existing designs for compliance to the latest directives and standards.
  • Oversee lab control and certifications.
  • Lead Safety and EMC testing projects with test labs -some local travel required.
  • During DCA, provide determination on what testing is needed with regards to Safety and EMC requirements.
  • Coordinate any required changes with mechanical, electrical, and software engineers.
  • Drive product certifications across development teams and testing labs.
  • Compile data and write reports regarding existing formal testing done at an accredited lab.
  • Prepare and / or edit test procedures to be used for EMC / Wireless formal evaluations.
  • Facilitate safety reviews of products systems and / or components as part of new product development and modify / update existing products.
  • Lead cross-functional teams to address product compliance related issues.
  • Define and lead all aspects of the hardware certification test requirements and validate testing reports for accuracy, completeness, and ensure all mandatory requirements are properly accounted for in complete package.
  • Stay current on relevant regulatory developments and new technologies.
  • Ensure appropriate technical documentation exists for each project (e.g., design history files, risk analysis reports, software development records, etc.).
  • Manage CAPA for product stewardship and electrical safety.

Requirements :

  • Bachelor's degree in engineering or related field from an accredited university or college.
  • Minimum 8 years' experience working on medical device software and hardware development projects.
  • Experience with ISO 14971, ISO 17025, IECEE procedures and audits, IEC 62304, Usability IEC 62368
  • Should be proficient in working with both IEC 62304 and IEC / EN 60601 for medical device manufacturing.
  • Working knowledge of regulatory requirements such as FDA 510(k) submissions and EU MDR / IVDR.
  • Strong understanding of development life cycle.
  • Experience with working with test labs, NRTLs (i.e. TUV, CSA, UL, etc.), updating technical files, and obtaining agency approvals.).
  • Attentiveness to details with strong organizational skills.
  • Ability to work proactively and independently.
  • Excellent communication skills, both written and verbal.
  • Must be able to communicate technical information effectively to both technical and non-technical personnel.
  • Travel Requirements :
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