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Post Market Quality Engineer (Robotics Surgical Technologies Post Market Engineer)

2 weeks ago
$28.00 - $32.00
Hourly

Company Name: Brooksource (working for a Fortune 50 medical device client)
Location: North Haven, CT, United States (Hybrid model – 3 days on-site, requires commute)
Job Type: Full-time, Contract
Salary Range: $28.00 – $32.00 hourly
Industry: Medical Devices / Robotics Surgical Technologies / Quality Engineering

Job Overview

Brooksource is a leading IT services and consulting firm dedicated to connecting top talent with impactful projects for premier organizations. We are seeking a highly motivated and detail-oriented Post Market Quality Engineer (Robotics Surgical Technologies Post Market Engineer) to join our team, supporting a Fortune 50 Medical Device client. This Entry-Level contract role offers a unique opportunity to contribute to the critical field of Quality Engineering within Robotics Surgical Technologies, ensuring the safety and performance of cutting-edge medical devices once they are in the market.

As a Post Market Quality Engineer, you will be instrumental in coordinating and conducting investigations into technical product issues, analyzing post-market trends, and ensuring rigorous regulatory compliance. You will play a vital role in upholding the highest quality standards for robotic surgical technologies, directly impacting patient safety and product reliability. If you possess strong analytical skills, a desire to learn and grow in a highly regulated industry, and are eager to make a tangible impact on advanced medical devices, Brooksource invites you to apply.

Duties and Responsibilities

  • Apply strong analytical and problem-solving skills to investigate and resolve complex product issues.
  • Demonstrate a strong commitment to upholding quality standards and regulatory compliance throughout all post-market activities.
  • Exhibit a strong desire to learn and grow both technically and professionally within the medical device and quality engineering domains.
  • Coordinate and conduct investigations on technical products, identifying root causes of defects and issues.
  • Actively manage defects, issues, and changes related to post-market product performance.
  • Perform in-depth analyzing post-market trends to identify emerging issues and risks.
  • Lead bi-monthly complaint analysis sessions, drawing insights and proposing corrective actions.
  • Create comprehensive weekly summaries of field performance for internal stakeholders.
  • Ensure strict regulatory compliance with FDA and ISO post-market analysis requirements.
  • Provide oversight to external AMS (Application Management Services) partners, ensuring their adherence to quality standards.
  • Align internal policies and procedures, focusing on software regulations, risk management, and change control.
  • Contribute to improving development processes based on post-market feedback and insights.
  • Provide guidance and training to service and support teams, specifically on Design Control principles.
  • Collaborate effectively across functions, including Service, Quality, Procurement, Marketing, R&D, and Operations.
  • Apply principles of project management, expectation setting, and best practices to all assigned tasks.

Qualifications

  • Experience Level: Entry-Level (0-2 years of relevant experience).
  • Education Requirement: Bachelor’s degree in a relevant field (e.g., engineering, quality management, life sciences).
  • Required Skills:
    • Strong analytical and problem-solving skills.
    • Commitment to upholding quality standards and regulatory compliance.
    • Desire to learn and grow both technically and professionally.
    • Ability to coordinate and conduct investigations on technical products.
    • Experience managing defects, issues, and changes.
    • Proficiency in analyzing post-market trends.
    • Ability to lead bi-monthly complaint analysis.
    • Skilled in creating weekly summaries of field performance.
    • Strong understanding of regulatory compliance (FDA and ISO post-market analysis requirements).
    • Capability to oversee external AMS partners.
    • Understanding of internal policies and procedures (software regulations, risk management, change control).
    • Interest in improving development processes.
    • Ability to provide guidance and training to service and support teams (Design Control).
    • Strong collaboration across functions (Service, Quality, Procurement, Marketing, R&D, Operations).
    • Knowledge of project management, expectation setting, and best practices.

Salary and Benefits

This Full-time, Contract Post Market Quality Engineer position offers a competitive hourly salary ranging from $28.00 – $32.00 hourly. Brooksource is dedicated to supporting our consultants, providing comprehensive benefits during the contract term. Benefits typically include health, dental, and vision insurance options, opportunities for professional development, and a supportive team environment focused on your success in this critical role within the medical device industry.

Working Conditions

This is a Full-time, Contract Hybrid position based in North Haven, CT, United States, requiring 3 days on-site each week. A reliable commute is essential. You will work within the client’s corporate environment, collaborating closely with various engineering, quality, and service teams. The role involves a mix of analytical work, investigations, documentation, and cross-functional meetings. The environment is fast-paced and highly regulated, typical of the medical device industry. When not on-site, you will operate from your home office, utilizing various software and communication tools for analysis and collaboration.

Why Work with Us

At Brooksource, we believe in connecting top talent with impactful projects that truly make a difference. For this Post Market Quality Engineer role, you’ll join a team contributing to a Fortune 50 Medical Device client, specifically within the cutting-edge field of Robotics Surgical Technologies. This presents a unique opportunity to apply your skills in Quality Engineering to ensure the safety and reliability of life-changing medical innovations.

You’ll gain invaluable experience in a highly regulated industry, working with complex technical products and collaborating with diverse teams. We offer a supportive environment where your desire to learn and grow is highly valued, and your contributions directly impact product quality and patient outcomes. If you are a driven Entry-Level professional seeking a challenging contract opportunity where your analytical skills and commitment to quality can truly make a difference in advancing medical technology, Brooksource offers the platform for your next significant career step.

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