Product Quality Engineer II

Hologic Careers•Newark, DE

1d•$78,000 - $122,100

About The Position

Are you passionate about ensuring the quality and reliability of life-saving medical devices? At Hologic, we are seeking a Product Quality Engineer 2 to provide engineering support for on-market medical devices. In this role, you’ll lead complaint investigations, perform root cause analyses, and implement corrective and preventive actions to improve product quality and compliance. Collaborating with cross-functional teams, you’ll drive process improvements, assess risks, and deliver impactful solutions that enhance patient safety and customer satisfaction. If you’re a proactive problem-solver with a strong background in quality engineering, we encourage you to apply and make a difference in healthcare innovation.

Requirements

Strong understanding of FDA Quality System Regulations, including Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP.
Familiarity with root cause analysis tools, risk management principles, and compliance frameworks.
Proven ability to lead complaint investigations, root cause analyses, and CAPA activities to resolve quality issues.
Strong data analysis and trending skills to identify risks, assess failure modes, and recommend mitigations.
Effective communication and presentation skills to articulate findings, root causes, and recommendations to stakeholders and leadership.
Ability to assess product changes for design and risk management impact, ensuring compliance and quality standards are maintained.
Proficiency in developing or improving testing methods for complaint investigations and technical activities.
Experience collaborating with cross-functional teams, including Operations, R&D, and Engineering, to drive product and process improvements.
Bachelor’s degree in Engineering (Mechanical, Biomedical, Biomechanical, Electrical, or related discipline) required.
2–5 years of experience in quality engineering, product development, or R&D, preferably in an FDA-regulated industry.
Hands-on experience in complaint investigations, root cause analysis, and CAPA activities.
Familiarity with internal and external audits, including Notified Body and FDA inspections.

Nice To Haves

Preferred knowledge of test method validation, statistical methods, design of experiments (DOE), and industry standards related to reliability, sterilization, packaging, and biocompatibility.
Familiarity with verification and validation requirements and the development of testable and measurable specifications.

Responsibilities

Lead complaint investigations
Perform root cause analyses
Implement corrective and preventive actions to improve product quality and compliance
Collaborate with cross-functional teams
Drive process improvements
Assess risks
Deliver impactful solutions that enhance patient safety and customer satisfaction