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    Manufacturing Engineering Manager - New York, United States - recruitAbility

    recruitAbility
    recruitAbility New York, United States

    1 week ago

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    Description


    Our client is a dedicated Austin-based, private equity-funded, medical device company that offers an innovative, FDA EUA-authorized, rapid PCR, point-of-care system.

    Their product is easy to use, affordable, and provides PCR results in only 15 minutes. They have a vision to enable simple, affordable, rapid, and accurate testing for everyone. They are an incredibly talented and diverse team of scientists, engineers, and experienced professionals who are driven to excel and significantly contribute to the world

    As they continue growing, they are looking for a

    Manufacturing Engineering Manager (Instrument)

    to lead the instrument manufacturing and instrument repair depot processes.

    This individual will be responsible for overseeing and managing the performance of all aspects of the manufacturing process, ensuring compliance with FDA regulations and GMP guidelines, and driving continuous improvement initiatives to optimize efficiency and product quality.

    What's in it for YOU?

    They offer a fast-paced, exciting, collaborative environment where individual contributions are highly valued as they work to expand the use of transformative testing technology in the market.

    A wonderful company culture with great core values and looking for team players who also align with them - Value Everyone, Ownership, Innovation, Collaboration, and Excellence Driven

    Very exciting time to work with an awesome leadership team that has proven experience commercializing biotech, including expertise in system and assay research and development, regulatory, intellectual property, engineering, and manufacturing.

    This company is in a growth mode and is bound for great things This is an opportunity for you to help make a significant difference with this delivery to the world

    What YOU get to DO at this growing company:
    Manage instrument and instrument repair depot manufacturing processes ensuring adequate resources, manufacturing capacity and planning as well as hiring and managing the direct labor and test technician operations
    Develop and implement required cGMP production processes and procedures.
    Develop and support production metrics and implement corrective actions as needed.
    Ensure strict adherence to FDA regulations and GMP guidelines through audits and daily oversight.
    Develop training documentation and plans for assembly team members.
    Collaborate with the Quality Assurance and Quality Control teams to address quality issues.
    Identify facility and equipment needs including oversight of facility projects and equipment installations.
    Identify opportunities for process optimization and efficiency improvements.
    Implement lean manufacturing principles to streamline operations.
    Lead continuous improvement projects.
    Oversee inventory levels to support production schedules
    Work with Commercial group to develop forecasts and production schedule.
    In line with company growth, hire, supervise and mentor a team of assembly personnel.
    Foster a culture of teamwork, accountability, and continuous improvement.
    Conduct performance evaluations and provide coaching to team members.
    Promote a safe working environment by enforcing safety protocols. Investigate and report safety incidents, implementing preventive measures.

    What you NEED to SUCCEED in this challenging role:
    Bachelor's degree in a relevant field, or equivalent years of education and experience required.
    At least 5 years of experience in manufacturing operations or equivalent role(s), preferably in the medical device industry.
    Experience operating in environments of FDA regulations and GMP guidelines preferred
    Excellent problem-solving and decision-making skills.
    Demonstrated ability to drive process improvements and cost reductions.
    Ability to work collaboratively, explain the 'Why,' and be able to influence others in a fast-paced environment.
    Ability to operate independently with moderate supervision.
    Ability to work cross-functionally to ensure all manufacturing objectives are met.
    Possess a high level of attention to detail and organization.
    Ability to prioritize tasks and to delegate them when appropriate.
    Proficient with Microsoft Office Suite or related software to complete reports and logs.
    Must be able to traverse the facility.
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