Junior Medical Quality Engineer

Introduction

At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life‑saving robots, our digital and software technology experts think outside the box as they provide unique R&D and engineering services across all industries. Join us for a career full of opportunities.

Where you can make a difference. Where no two days arethe same

This is an onsite role in Pittsburgh, PA

This is a Medical Junior Quality Engineer role, to perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Supports design quality activities throughout new product development, including design reviews, requirements review, risk management, verification and validation planning, and design transfer readiness.
• Supports design transfer activities by ensuring product and process requirements are translated into manufacturing, inspection, supplier, validation, and release deliverables.
• Lead and participate in Design Failure Modes and Effects Analysis (DFMEA) and risk assessments.
• Participate in DFMEA, PFMEA, process flow, control plan, and risk assessment activities to ensure design and manufacturing risks are identified, mitigated, and documented.
• Review protocols and participate in V&V planning to ensure alignment with product requirements.
• Review verification, validation, inspection, equipment qualification, and process validation protocols to ensure alignment with product requirements, risk controls, and design transfer needs.
• Participate in protocol review and support testing strategy, ensuring robust verification and validation processes.
• Support execution and documentation of equipment qualification and process validation activities, including IQ/OQ/PQ, validation reports, and related production readiness evidence.
• Support Design Control activities by ensuring compliance with FDA and international regulations.
• Support supplier/process readiness activities, including review of supplier documentation, inspection results, capability studies, MSA/Gage R&R, and approval packages.
• Develop and execute supplier qualification processes, including supplier contracts and PPAPs.
• Develops various inspection techniques and procedures to ensure product integrity to design specifications.
• Responsible for the writing, approval and implementation of Incoming, In-Process and Final Inspection procedures and operator self-inspection procedures.
• Works with other Quality Engineers and the Metrology Lab personnel on the development of all product gaging.
• Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, assists each of these groups with capability studies and the application of statistical quality control.
• Interfaces with Manufacturing Engineers to review processes for new products and coordinate process validations and capability studies.
• Recommends process monitoring devices where applicable.
• Assists with complaint investigation and documentation interfaces with Regulatory Affairs to support UL, IEC, and FDA submissions.
• Participates in internal audits conducted by internal employees and regulatory agencies.
• Manage and drive timely resolution of nonconformances (NCs) and corrective & preventive actions (CAPAs).

• Bachelor’s degree in Engineering, Quality, or a related field (Master’s preferred).
• 3+…