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    Senor Packaging and Labeling Development Engineer - Minneapolis, United States - Johnson & Johnson

    Johnson & Johnson
    Johnson & Johnson Minneapolis, United States

    21 hours ago

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    Description
    Job Description - Senor Packaging and Labeling Development Engineer W)
    Senor Packaging and Labeling Development Engineer

    W
    Description

    Sterilmed Inc., a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Senior Packaging and Labeling Development Engineer, located in Plymouth, MN.

    At Johnson & Johnson,we believe health is everything.

    Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

    Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

    Learn more at

    We are offering a fantastic opportunity for an engineer to join our team and play a vital role in the development and improvement of new products and processes throughout their life cycle.

    In this position, you will have direct involvement with new product development, as well as collaborating with our Research & Development team to ensure the validation of packaging configurations and labeling contents in line with FDA requirements.

    As a successful candidate, you will work closely with members of our design and sustaining teams, forming an integral part of a core team striving to achieve project goals.


    Your responsibilities will encompass supporting two teams:

    firstly, improving the quality and compliance of our existing products and designs, and secondly, leading the vital testing for the development and validation of new packaging configurations and labels.

    At Sterilmed, we are recognized as authorities in medical device reprocessing, focusing primarily on high-complexity devices such as electrophysiology and imaging catheters.

    This role will involve some travel between our manufacturing, distribution, and receiving sites located in the metro-Minneapolis area.
    A Day in the Life
    Develop, design, and validate packaging and labeling per requirements
    Lead and coordinate validation of package components, labeling components, and packaging processes
    Partner with design team to deliver packaging components for R&D and packaging projects
    Evaluate new package concepts and technologies
    Identify processing needs, develop packaging specifications, procure equipment and materials
    Lead process improvement and task teams, supporting continuous improvement efforts
    Investigate and implement corrective/preventive actions for manufacturing processes
    Author, revise, and provide support for production work instructions
    Support regulatory partners in approval efforts and Master Data Management processes
    Ensure compliance with regulations, policies, procedures, and staff Health, Safety, and Environmental guidelines if applicable
    Qualifications

    Required
    Bachelor's degree in engineering field (Biomedical, Packaging, Manufacturing, Mechanical, Industrial, etc.)
    Minimum of 4 to 6 years packaging engineering responsibilities in ISO13485/GMP environment
    Prior experience in the medical device industry is preferred
    May require up to 10% travel
    Preferred
    Proficiency in Microsoft Office and excellent technical written and oral communication skills.
    Experience with statistical analysis, including DOE, FMEA, QSR, process capability studies, and validation methodology, with knowledge of statistical software.
    Familiarity with ASTM and other packaging standards, working within an ISO structured quality system.
    Strong planning, multi-tasking, and project management skills with a consistent record of completing projects on time and accomplishing goals.
    Ability to work independently as well as part of a team, leading multiple priorities in a fast-paced environment.
    Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

    For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit
    Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

    All qualified applicants will receive considerationfor employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin,or protected veteran status and will not be discriminated against on the basis of disability.andEqual Employment Opportunity Posters GINA Supplement.

    If you are an individual with a disability, please check ourpage for information on how to request an accommodation.
    Disability Assistance
    This site is governed solely by applicable U.S. laws and governmental regulations. Please see our. Use of this site constitutes your consent to application of such laws and regulations and to our. Your use of the information on this site is subject to the terms of our.

    You should view thesection and the most recent SEC Filings in thesection in order to receive the most current information made available by Johnson & Johnson Services, any questions or search this site for more information.

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