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    Training Specialist - Roseville, United States - Penumbra

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    Description

    Come be part of the Training team at Penumbra, a company dedicated to saving lives.


    In the role of a Training Specialist, you will be involved in developing and executing training programs to enhance the stability and growth of our Production environments.
    Perform assigned tasks to increase knowledge and understanding of GMP and Production processes.


    Current programs you will work on:
    New Hire Orientation, Train the Trainer, Quality System (QSR) initiatives, etc.

    Develop and keep up-to-date existing programs and materials, and create new programs according to identified future needs from various sources.

    This position requires working hours from 3 pm to 11:30 pm.

    Specific Duties and Responsibilities

    • Develop and update current training materials
    • Present information using various instructional techniques, tools, and formats
    • Conduct and/or co-facilitate professional development, computer skills, software orientation, and training programs for employees
    • Coordinate support, facilitate, and grade written and microscope exams during company job fairs
    • Provide training on SOPs, WIs, and Quality System requirements to incoming product builders
    • Coordinate required training with cross-functional groups as specified in ECOs for changes to SOPs, WIs, and MQIs in the manufacturing area
    • Verify training records for completeness and accuracy
    • Handle training record inquiries via the Service Now Help Desk System
    • Organize and deliver data using Microsoft Excel, PowerPoint, and TurningPoint software
    • Resolve process and/or documentation issues, including the initiation and implementation of change requests
    • Maintain clean room standards, practices, and housekeeping according to standard operating procedures and the illness and injury prevention program
    • Ensure completion of personnel training records
    • Follow the Company's Quality Management System (QMS) and domestic and global quality system regulations, standards, and procedures
    • Ensure department members comply with the QMS, regulations, standards, and procedures
    • Perform other assigned work-related duties
    Position Qualifications

    • High School or GED, plus five years of manufacturing experience in the medical device, pharmaceutical, or biotech industry, or an equivalent combination of education and experience
    • Two or more years of learning and development or training experience
    • Excellent verbal, written, and interpersonal communication skills
    • Basic math skills, proficiency with Microsoft Word, Excel, Access, and Power Point
    • Strong attention to detail, organization, and teamwork
    • Basic knowledge of cGMP/QSR requirements
    • Ability to work both day and swing shift preferred

    Day shift hours: 6 am to 2:30 pm, Swing shift hours: 3 pm to 11:30 pm

    Working Conditions

    • Various office, laboratory, and cleanroom environments
    • Potential exposure to blood-borne pathogens
    • Some lifting and moving of up to 25 pounds
    • Frequent standing, walking, sitting; using a computer, sitting for extended periods
    • Specific vision abilities required include reading, color, peripheral and depth vision
    Annual Base Salary Range:
    $66 - $84, differential


    We provide a competitive compensation package along with excellent benefits and equity programs when applicable.

    Actual total compensation will differ based on qualifications, skill level, competencies, and work location.

    What We Offer

    • A collaborative teamwork environment where learning is continuous and performance is recognized
    • Join the team leading the way in revolutionizing the treatment of severe diseases globally
    • Generous benefits package for eligible employees, including medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, employee stock purchase plan, paid parental leave, company holidays, accrued vacation, and sick time

    Penumbra, Inc., based in Alameda, California, is a leading global healthcare company focusing on innovative therapies.

    Penumbra innovates, produces, and markets unique products to address challenging medical conditions with significant unmet requirements.

    Penumbra sells its solutions to healthcare providers mainly through its direct sales network in the United States, Europe, Canada, and Australia, supplemented by distributors in some international markets.

    The Penumbra logo is a registered trademark of Penumbra, Inc.

    Qualified candidates will be considered for employment regardless of race, color, religion, gender, national origin, sexual orientation, age, disability, military or veteran status, or any other protected characteristic under laws.

    If you are a California resident, please review Penumbra's Privacy Notice.

    For more details about Penumbra's commitment to being an equal opportunity employer, refer to Penumbra's AAP Policy Statement.


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