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    Quality Engineer - Hudson, United States - H.B. Fuller

    H.B. Fuller
    H.B. Fuller Hudson, United States

    3 weeks ago

    Default job background
    Description
    As the largest pureplay adhesives company in the world, H

    B Fuller's (NYSE:
    FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day.

    Founded in 1887, with 2023 revenue of $3.5 billion, our mission to Connect What Matters is brought to life by more than 7,000 global team members who collaborate with customers across more than 30 market segments in over 140 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets.

    H.B. Fuller acquired Adhezion Biomedical, LLC which is a medical device company engaged in the development, manufacturing and commercialization of

    highly-differentiated,

    proprietary, cyanoacrylate-based adhesive and infection prevention products.
    Quality Engineer that will work with our Operational quality team.

    This individual will own all quality activities for their assigned product lines and may be working on multiple different products lines at once.

    They will be assigned to products for new product development and work closely with internal team and Contract Manufacturer on each product.

    Support Design Engineering and Manufacturing Operations by developing manufacturing processes, work instructions, fixtures, and production equipment.
    This individual will be reporting to the Quality Manager for HHC Hygiene Global.

    Primary Responsibilities:
    Manage validation program – IQ,OQ, PQ, & Gage R&Rs.
    Support projects related to lean manufacturing plant layout, process to ensure efficient and timely completion.
    Assist with design transfer to manufacturing, including quality control activities from production processes to shipment of the final product.
    Work with Contract Manufacturer (CM) to review existing process and implement new manufacturing processes.
    Inspect product including labeling and documentation for release of finished goods.
    Manage product traceability and labeling.
    Manage and maintain product device history records.

    Ensure that all production employees are familiar with, trained on, and follow all manufacturing procedures related to their jobs Ensure that changes to procedures are reviewed, approved and validated prior to implementation.

    Oversee creation and review of documentation for nonconforming product.
    Lead product investigation related to customer complaints and corrective actions.
    Works with Engineering department ensuring that engineering change orders affecting production related changes are reviewed.
    Assist with revisions and updates to quality procedures, standardized work instructions.
    Maintain equipment calibration program to ensure equipment is calibrated in a timely manner.
    Participate in supplier management activities. Identify supplier issues.
    Assist with APQP and Risk Management Documentation.
    Support Internal Quality Audit.
    Support 3rd party audit and inspection activities.
    Coordinate and Support Weekly Inspection of Facilities, Daily Facility Walks and Bioburden & Particulate Assessment.
    Identify, Communicate, Drive & Support Resolution of Quality Issues as Identified in the Production Area.
    Support Sterility Management Program.
    Support Document Control & Lab Functions.
    Champion cGMP – General Omnsbudman for Production.
    BS degree in manufacturing, mechanical, industrial or process engineering, highly desired
    Minimum of 2 years' experience (5+ years preferred) in manufacturing engineering in a process driven manufacturing environment
    Hands-on experience troubleshooting equipment
    Proficient with SolidWorks or equivalent 3D CAD software
    Working knowledge of Microsoft Office products (Work, Excel, Outlook, PowerPoint)
    Ability to multi-task and meet deadlines in a fast-paced environment
    Ability to communicate effectively and professionally with internal and external parties
    Ability to work in a team environment

    Physical Environment and Requirements:
    Standing on concrete floors for several hours at a time.
    Essential physical requirements, such as climbing, standing, stooping or typing.
    Lifting up to 30 pounds.
    Work in loud/chaotic environments.
    Wear appropriate PPE such as mask, goggles, footwear as applicable.
    The ability to see and respond to situations.
    Pay is based on several factors including but not limited to education, work experience, certifications, and geographic location.
    The salary for this role is $85, ,000.

    As the largest pureplay adhesives company in the world, H

    B Fuller's (NYSE:
    FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day.

    Founded in 1887, with 2023 revenue of $3.5 billion, our mission to Connect What Matters is brought to life by more than 7,000 global team members who collaborate with customers across more than 30 market segments in over 140 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets.

    H.B. Fuller acquired Adhezion Biomedical, LLC which is a medical device company engaged in the development, manufacturing and commercialization of

    highly-differentiated,

    proprietary, cyanoacrylate-based adhesive and infection prevention products.
    Quality Engineer that will work with our Operational quality team.

    This individual will own all quality activities for their assigned product lines and may be working on multiple different products lines at once.

    They will be assigned to products for new product development and work closely with internal team and Contract Manufacturer on each product.

    Support Design Engineering and Manufacturing Operations by developing manufacturing processes, work instructions, fixtures, and production equipment.
    This individual will be reporting to the Quality Manager for HHC Hygiene Global.

    Primary Responsibilities:
    Manage validation program – IQ,OQ, PQ, & Gage R&Rs.
    Support projects related to lean manufacturing plant layout, process to ensure efficient and timely completion.
    Assist with design transfer to manufacturing, including quality control activities from production processes to shipment of the final product.
    Work with Contract Manufacturer (CM) to review existing process and implement new manufacturing processes.
    Inspect product including labeling and documentation for release of finished goods.
    Manage product traceability and labeling.
    Manage and maintain product device history records.

    Ensure that all production employees are familiar with, trained on, and follow all manufacturing procedures related to their jobs Ensure that changes to procedures are reviewed, approved and validated prior to implementation.

    Oversee creation and review of documentation for nonconforming product.
    Lead product investigation related to customer complaints and corrective actions.
    Works with Engineering department ensuring that engineering change orders affecting production related changes are reviewed.
    Assist with revisions and updates to quality procedures, standardized work instructions.
    Maintain equipment calibration program to ensure equipment is calibrated in a timely manner.
    Participate in supplier management activities. Identify supplier issues.
    Assist with APQP and Risk Management Documentation.
    Support Internal Quality Audit.
    Support 3rd party audit and inspection activities.
    Coordinate and Support Weekly Inspection of Facilities, Daily Facility Walks and Bioburden & Particulate Assessment.
    Identify, Communicate, Drive & Support Resolution of Quality Issues as Identified in the Production Area.
    Support Sterility Management Program.
    Support Document Control & Lab Functions.
    Champion cGMP – General Omnsbudman for Production.

    Minimum Requirements:
    BS degree in manufacturing, mechanical, industrial or process engineering, highly desired
    Minimum of 2 years' experience (5+ years preferred) in manufacturing engineering in a process driven manufacturing environment
    Hands-on experience troubleshooting equipment
    Proficient with SolidWorks or equivalent 3D CAD software
    Working knowledge of Microsoft Office products (Work, Excel, Outlook, PowerPoint)
    Ability to multi-task and meet deadlines in a fast-paced environment
    Ability to communicate effectively and professionally with internal and external parties
    Ability to work in a team environment

    Physical Environment and Requirements:
    Standing on concrete floors for several hours at a time.
    Essential physical requirements, such as climbing, standing, stooping or typing.
    Lifting up to 30 pounds.
    Work in loud/chaotic environments.
    Wear appropriate PPE such as mask, goggles, footwear as applicable.
    The ability to see and respond to situations.
    Pay is based on several factors including but not limited to education, work experience, certifications, and geographic location.
    The salary for this role is $85, ,000. In addition to your salary, H.B.

    Fuller offers employees a competitive total rewards package including comprehensive benefits, incentive and recognitions programs, health & wellness benefits, 401K contributions, paid time off and paid holidays.

    Eligibility may vary.
    H.B.

    Fuller is an Equal Employment Opportunity employer and proud to have created a collaborative culture where employees around the world are seen, heard, and respected.

    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, or marital status or status as a protected veteran, or any other legally protected classification.

    H.B. Fuller does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with H.B.

    Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate.

    Without a signed service agreement, H.B. Fuller shall not be obligated for payment of any fee or compensation.

    About Us

    For 130 years, H.B.

    Fuller has been a leading global adhesives provider focusing on perfecting adhesives, sealants and other specialty chemical products to improve products and lives.

    H.B.

    Fuller's commitment to innovation brings together people, products and processes that answer and solve some of the world's biggest challenges.

    Our reliable, responsive service creates lasting, rewarding connections with customers in electronics, disposable hygiene, medical, transportation, clean energy, packaging, construction, woodworking, general industries and other consumer businesses.

    And our promise to our people connects them with opportunities to innovate and thrive.

    #J-18808-Ljbffr

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