Principal Design Quality Engineer I

Job Summary

Nova Biomedical is seeking a Principal Design Quality Engineer I to support the development of innovative, high-performance diagnostic and analytical technologies used in clinical care, critical care, bioprocessing, and life science research. This role plays a central part in ensuring Nova Biomedical’s in-vitro diagnostic products are safe, effective, compliant, and built on robust design principles.

Responsibilities

• Serve as the Design Quality representative on cross-functional product development teams, ensuring compliance with 21 CFR 820, ISO 13485, IVDR, and other applicable standards.
• Lead and maintain Design Control activities, including design plans, design reviews, risk management files, verification/validation strategy, and design transfer documentation.
• Develop, review, and approve risk management documentation in accordance with ISO 14971, including hazard analyses, FMEAs, and risk-benefit assessments.
• Partner with R&D to ensure design inputs are clear, testable, and aligned with user needs and regulatory expectations.
• Review and approve engineering documentation such as specifications, test protocols, test reports, and design changes.
• Support verification and validation activities, including method development, statistical justification, and traceability.
• Drive root cause investigations and corrective/preventive actions related to design issues, nonconformances, and field performance.
• Support supplier quality activities for design-critical components, including qualification and change assessments.
• Contribute to continuous improvement of the Quality Management System, with a focus on design-related processes.
• Participate in internal and external audits, providing subject matter expertise on design controls and IVD product development.

Experience Requirements

• Bachelor’s degree in Engineering, Life Sciences, or a related technical field required.
• 3–7+ years of experience in medical device or IVD product development, with direct involvement in design controls.
• Strong working knowledge of 21 CFR 820, ISO 13485, ISO 14971, and IVD-specific regulatory expectations.
• Experience with risk management, verification/validation, and design documentation.
• Able to interpret engineering drawings, specifications, and test data.
• Excellent communication skills and comfort working cross-functionally.
• Experience with IVD assays, instrumentation, software-driven diagnostics, or reagent/consumable development.
• Familiarity with IVDR requirements preferred.
• Background in statistics, DOE, or analytical method validation preferred.
• Experience in a fast-paced, early-stage, or growth-stage biotech environment preferred.

Physical Requirements And Working Conditions

• Ability to stand or sit for extended periods.
• Manual dexterity required for handling laboratory equipment and instrumentation.
• Ability to lift and carry up to 25 pounds.
• Ability to perform repetitive tasks.
• Ability to work in a laboratory environment with exposure to chemicals or biological materials.
• Ability to use required personal protective equipment (PPE).
• Occasional bending, reaching, or movement within lab environment.

About The Company

Nova Biomedical is a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.