[Hiring] Engineer Sr. I - QA Design @Arthrex

Arthrex; Deutschland; Remote; EUR 93.000 - 134.000; Vollzeit

Zusammenfassung

A global medical device company is hiring a remote Engineer Sr. I - QA Design. This role focuses on quality assurance in design development of medical devices, requiring a Bachelor's degree in Engineering and 5+ years' related experience. Key responsibilities include leading design assurance efforts and ensuring compliance with standards. The position offers a competitive salary and various benefits including medical insurance and a 401(k) retirement plan.

Leistungen

Medical, Dental and Vision Insurance

Company-Provided Life Insurance

Voluntary Life Insurance

Flexible Spending Account (FSA)

Supplemental Insurance Plans

Matching 401(k) Retirement Plan

Annual Bonus

Wellness Incentive Program

Free Onsite Lunch

Gym Reimbursement Program

Tuition Reimbursement Program

Paid Parental Leave

Paid Time Off

Paid Sick Leave

Volunteer PTO

Employee Assistance Provider (EAP)

Qualifikationen

• Bachelor’s degree in Engineering required; Biomedical, Mechanical, or Electrical Engineering degree preferred.
• 5 years design assurance/quality assurance experience in a medical device or other highly regulated industry required.

Aufgaben

• Lead design assurance efforts for new product introduction projects.
• Ensure compliance with national and international regulations.
• Supervise the design assurance team and coordinate work.
• Conduct product risk assessment activities.
• Facilitate verification/validation activities.
• Establish and maintain Risk Management File(s).

Jobbeschreibung

Overview

Sep 06, 2025 - Arthrex is hiring a remote Engineer Sr. I - QA Design. Salary: USD 109,250 - 156,687 per year. Location: Remote, USA. Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. The Engineer Sr. I - Design Assurance is responsible for various Quality Assurance functions and design development activities of Class I and II medical devices in compliance with FDA, ISO, CMDR Quality Systems and Design Control requirements. The position requires a Bachelor’s degree in Engineering and 5+ years of experience in Quality Control or Quality Assurance.

This position is eligible for remote work.

Essential Duties and Responsibilities

• Lead design assurance efforts within product design and development for new product introduction projects with an emphasis in quality aspects of integrated software, electrical, and/or mechanical device characteristics, as appropriate for the specific area of position focus.
• For electrical equipment / active device projects, lead compliance efforts for electrical safety, environmental, and emissions in accordance with national and international regulations.
• Ensure appropriateness of documented design requirements and outputs while ensuring traceability throughout the product development lifecycle.
• Provide active leadership in understanding and implementing regulations/standards, acting as a resource to other disciplines, within the product design process from idealization through product retirement.
• Supervise, assign, and coordinate others / the work of others within the design assurance team to support the department and design projects and goals.
• Provide input into and lead addressing of lessons learned to support development, modification, and improvement of design processes and quality management system.
• Lead product risk assessment activities through application of a working knowledge of applicable standards (e.g., ISO14971, etc.) and tools such as FMEAs, FTA, and Hazard Assessment.
• Display working knowledge and provide guidance to design teams in the area of usability/human factors engineering principles including standards (IEC 62366) and FDA guidance for compliance.
• Facilitate the planning, execution, and review of verification/validation activities including assessment of adequate inputs to the v&v process.
• Lead and coordinate the design assurance aspects of Design to Manufacture Transfer including generation of inspection methods, drawing reviews, determining key product indicators/essential requirements and, where appropriate, training of manufacturing personnel in appropriate test procedures, inspection methods, and interpretation of results.
• Ensure required outputs of the design control process are met, including compliance of the design history file (DHF), and support transition of the design project into sustaining engineering.
• Support design-related corrective and preventative activities for projects in the pre-sustaining phase.
• Establish and maintain Risk Management File(s).

Education and Experience

• Bachelor’s degree in Engineering required; Biomedical, Mechanical, or Electrical Engineering degree preferred.
• 5 years design assurance/quality assurance experience in a medical device or other highly regulated industry required.

Knowledge and Skills

• Working knowledge of ISO and FDA design and development quality requirements.
• Technical knowledge in development methodologies, design quality analysis, and project implementation.
• Proficiency in assessing manufacturing quality requirements of new product concepts.
• Technical knowledge in development methodologies, design, and project implementation, including but not limited to, GD&T & DOE preferred.
• Experience in DHF & Technical File structure and maintenance.
• Basic knowledge in Electro-Medical safety standards - IEC 60601-1 (Electrical safety), IEC 60601-1-2 (EMC), and other Collateral and Particular standards.
• Hands-on experience and knowledge in global medical device regulatory requirements for Electro-Surgical Devices.
• Essential knowledge of Risk Management for medical devices (per ISO 14971).

Machine, Tools, and Equipment Skills

• Proficiency with PC operations, and the Microsoft Office suite. Hands-on experience with Minitab, SAP, Codebeamer and Windchill preferred.

Reasoning and Mathematical Skills

• Reasoning: Ability to define problems, collect data, establish facts, and draw valid conclusions; interpret a wide range of technical instructions.
• Mathematical: Ability to apply mathematical principles as required by the role.

Language and Communication Skills

• Ability to comprehend and apply language skills to perform the job; effective verbal communication with team members and management; ability to write and record data as required by procedures.

Benefits

• Medical, Dental and Vision Insurance
• Company-Provided Life Insurance
• Voluntary Life Insurance
• Flexible Spending Account (FSA)
• Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
• Matching 401(k) Retirement Plan
• Annual Bonus
• Wellness Incentive Program
• Free Onsite Lunch
• Gym Reimbursement Program
• Tution Reimbursement Program
• Paid Parental Leave
• Paid Time Off
• Paid Sick Leave
• Volunteer PTO
• Employee Assistance Provider (EAP)

Equal Opportunity

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.