Product Development Compliance Engineer

 

The Product Compliance Engineer will partner with global product developers and certification partners on regulatory compliance and product certification. The candidate will support certification projects from product concept to mass production, ensuring market access requirements are met and that product designs incorporate appropriate risk mitigation solutions. This role includes participation in medical device regulatory pathways alongside our consumer and commercial product portfolio.

Here are some of the EXCITING things you'll get to do:

· Support the execution of certification activities and risk analysis for multiple new product development projects, including FDA-regulated medical devices and products subject to EU MDR 2017/745.

· Assist in preparing regulatory filings including FDA 510(k) submissions and Technical Files/Design Dossiers, and maintain Design History Files (DHF) in compliance with 21 CFR Part 820 Design Controls and ISO 13485 requirements.

· Support the establishment of project needs and deliverables for both product development teams and third-party regulatory partners, including Notified Bodies and FDA-accredited testing laboratories.

· Execute risk management activities in accordance with ISO 14971, including hazard identification, risk estimation, risk evaluation, and residual risk documentation across the product lifecycle.

· Support usability engineering processes per IEC 62366-1, including participation in formative and summative evaluation planning for medical device products intended for home healthcare environments.

· Evaluate project risk during the development process and support contingency planning to overcome obstacles, including regulatory strategy adjustments driven by classification questions or design changes.

· Participate in weekly reviews for all assigned projects, presenting status and associated project risks including certification timelines and Notified Body or FDA feedback cycles.

· Assure that all activities related to product certification commence and execute as planned and on schedule, with attention to FDA review timelines and CE marking milestones under EU MDR.

· Support product development teams as a subject matter expert, providing counsel on medical device-specific requirements including biocompatibility (ISO 10993 series), software lifecycle (IEC 62304), and home healthcare electrical safety (IEC 60601-1-11).

· Contribute to intradepartmental continuous improvement and special projects, including post-market surveillance and complaint handling processes under 21 CFR Part 803 and EU MDR.

Attributes & Skills

· Bachelor's degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, Systems Engineering, Materials Engineering, Computer Science, or a related technical discipline; RAC certification a plus.

· Relevant discipline context: Biomedical/Bioengineering backgrounds are well-suited to ISO 10993 biocompatibility and clinical evaluation; Systems Engineering to ISO 14971 risk management and design controls; Chemical/Materials Engineering to material selection, substance compliance (REACH, RoHS), and biocompatibility testing; Computer Science/Software Engineering to IEC 62304 software lifecycle and embedded systems compliance.

· Minimum 2–4 years of compliance or design-related experience with consumer, commercial, or medical electromechanical products.

· Working knowledge of medical device regulatory standards including:

· IEC 60601-1 and applicable collateral/particular standards (esp. IEC 60601-1-2 for EMC, IEC 60601-1-6 for usability, IEC 60601-1-11 for home healthcare environments)

· ISO 14971 – Risk Management for Medical Devices

· ISO 13485 – Quality Management Systems

· IEC 62366-1 – Usability Engineering

· IEC 62304 – Medical Device Software Lifecycle (where applicable)

· ISO 10993 series – Biocompatibility Evaluation

· 21 CFR Part 820 – FDA Quality System Regulation

· EU MDR 2017/745 – classification rules, Technical Documentation, and UDI obligations

· FDA 510(k) submission processes

· Familiarity with international medical device regulations for key markets (Health Canada, TGA Australia, ANVISA Brazil) preferred.

· Experience with DFMEA and medical-grade risk management documentation (hazard analysis, risk control verification, residual risk justification).

· Exposure to or experience interfacing with FDA, Notified Bodies, or accredited test laboratories preferred.

Must be able to:

· Operate comfortably in a fast-paced environment with regularly shifting priorities, including simultaneous consumer and regulated-device program timelines.

· Thrive under pressure and want to be continuously challenged.

· Manage multiple projects simultaneously while maintaining continuous track of key details, including regulatory submission status and design change impact assessments.

· Multi-task, maintaining a comprehensive understanding of project status across consumer certification and medical device regulatory workstreams.

· Present creative and technically sound solutions to complex problems, including regulatory pathway questions where classification is ambiguous.

· Like to "solve the puzzles" and deliver on challenging assignments.

· Analyze operations and support continuous improvement initiatives within a design control and post-market surveillance framework.

· Work with conviction while collaborating and compromising where appropriate.

· Work and think with moderate supervision and generate ideas within their area of expertise.

· Make sound decisions utilizing all available information, including benefit-risk trade-offs required under ISO 14971.

· Communicate complex technical and regulatory information to audiences with varying technical understanding.

· Adapt well to change, including evolving regulatory guidance and new product category entries into regulated spaces.

· Present confidently to colleagues and leadership across the organization.

· Desire ownership and possess a "want to take the last shot of the game" mentality.