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    Manufacturing Quality Engineer - Natick, United States - Allurion

    Allurion
    Allurion Natick, United States

    2 weeks ago

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    Description
    Why Allurion?


    We are overjoyed to be recognized as one of Deloitte's top 500 fastest-growing technology companies in the US But wait, there's even more excitement in store Get ready for an incredible new journey as we proudly announce our official public listing ALUR.

    This momentous milestone opens up a new era filled with boundless possibilities and remarkable growth for our company

    At Allurion, our core values of Audacity, Grit, Authenticity, Accountability, and being Data Driven, combined with our passion for innovation, have fuelled our growth and will help us achieve our ambitious mission - ending obesity As part of a recognized Great Place to Work


    in the US, UK, France, Allurions engage as a collaborative global team while solutioning a critical healthcare challenge which affects millions.

    We are driven by purpose, motivated by individual challenge and growth, and energized by collective engagement and competitive rewards.

    We invite you to join us as we aim to transform the way obesity is treated and make a lasting impact on the world.

    What will you be doing?


    As a Manufacturing Quality Engineer reporting to the Director of Quality Assurance, you'll play a pivotal role in supporting Allurion's manufacturing facility.

    Your responsibilities will involve collaborating closely with various departments to identify and implement enhancements to our manufacturing line.

    You'll take charge of tasks such as data collection, review, and the implementation of electronic systems aimed at reducing paperwork and enhancing data dissemination capabilities.


    What we're looking for in you:

    Bachelor's Degree Requirement:


    A bachelor's degree in biomedical/mechanical engineering or a related technical field is a minimum requirement for this role, ensuring a solid foundation in the necessary expertise.


    Extensive Experience:


    With at least 5 years of experience in medical device manufacturing, candidates bring a wealth of knowledge and expertise to the table, contributing to the continued success of our operations.


    Regulatory Compliance:


    Demonstrated experience in quality operations within highly regulated industries, particularly with ISO 13485, ISO 14644, and FDA regulations, ensures adherence to rigorous standards and compliance with industry regulations.


    Collaborative Skills:


    Exceptional interpersonal and communication skills, coupled with the ability to collaborate effectively across diverse teams, are essential for fostering a culture of cooperation and achieving collective goals.


    Proactive Problem-Solving:


    Goal-oriented individuals with a positive attitude and a proactive approach to problem-solving exhibit the initiative and creativity necessary to address challenges efficiently and with attention to detail.


    Hands-On Expertise:


    Proficiency in hands-on troubleshooting and problem-solving allows for practical solutions to issues that may arise, ensuring smooth operations and timely resolutions.


    Adaptability:


    The ability to manage multiple assignments in a dynamic, fast-paced environment with shifting priorities demonstrates adaptability and agility in meeting organizational needs.


    Professionalism:


    Upholding high standards of professionalism fosters a culture of excellence and integrity within the workplace, contributing to a positive and respectful work environment.


    Technical Proficiency:


    Confidence in utilizing Microsoft Windows, Microsoft Office, and Adobe Acrobat, as well as proficiency in basic mathematics and statistics, ensures proficiency in essential tools and analytical capabilities.


    Continuous Improvement:
    Familiarity with Six Sigma methodologies is advantageous, reflecting a commitment to continuous improvement and optimization of processes.


    What's in it for you:
    Competitive Package
    Paid Time Off
    Training and Career Development
    Global Employee Assistance Program & Total Wellbeing Platform
    Employee Stock Purchase Program
    Volunteer Time Off
    Benefits and perks are tailored to your country of residence


    Location:

    Located in Natick:
    Onsite full-time.

    At Allurion, we thrive on the balance of virtual connections and face-to-face interactions, nurturing a vibrant culture of collaboration and innovation among our diverse global team.


    Hours:


    Let's kickstart the day, maximizing our workday with ample time for lunch to recharge and refuel We're all about balance here, so your work experience will be tailored to support your best self, allowing you the flexibility you need.

    Your well-being matters to us

    Diversity and Inclusion

    Allurion is committed to a fair hiring process free from discrimination and we welcome candidates from all backgrounds. If your experience is close (even if not a perfect fit) to what we're looking for, please consider applying. Experience comes in many forms - skills are transferable, and passion goes a long way. We know that diversity makes for the best problem-solving and creative thinking, which is why we're dedicated to adding new perspectives to the team and encourage everyone to apply

    To learn more about Allurion please visit our website

    #LI-onsite
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