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    Production Planning Coordinator - Hamilton, ON, Canada - Allergan

    Allergan
    Allergan Hamilton, ON, Canada

    1 week ago

    Default job background
    Description
    Manufacturing Supervisor 1st Shift M-F (9:00am-5:00pm)

    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.

    We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.

    Follow @abbvie onTwitter ,Facebook ,Instagram ,YouTube andLinkedIn .

    In this role, you will lead a team of 25 employees in the material management department, focusing on ensuring safety, quality, productivity, and efficient product movement to support our cGMP manufacturing operations.

    You will collaborate with your team to maintain quality compliance, resolve production performance issues, and analyze staffing needs to support our 24/7 operations.

    Additionally, you will play a key role in developing and updating Standard Operating Procedures and maintaining inventory accuracy.

    If you are a dedicated and experienced professional with a passion for driving continuous improvement and maintaining quality compliance, we encourage you to apply for the Supervisor of Material Management position.

    Lead a team of 25 employees in a collaborative environment to drive continuous improvement and maintain quality compliance.
    Analyze material management staffing needs to support 24/7 production operations and make business decisions based on volume changes.
    Coordinate training and ensure 100% training compliance in an FDA regulated environment.
    Prepare, compile, and review documentation for production processing for completeness and accuracy.
    Maintain inventory accuracy and appropriate stock levels for all production supplies and tissue.
    Ensure cleaning and housekeeping of production areas are in compliance.
    Prioritize activities to achieve planning and business objectives while fostering positive engagement throughout the organization.
    Support the development of site strategy and process improvements to achieve long-term business objectives.

    Work cross-functionally to support all business initiatives, including OpEx, special projects, production training, talent acquisition, talent development, goal setting, and performance development.

    Requires a Bachelor's degree or equivalent; Eight plus years' experience in all aspects of manufacturing/ production processes
    Computer proficiency and scheduling experience required; good writing skills.
    Working knowledge of safety, quality systems, and cGMPs is required
    Familiarity with industrial automation (e.g., distributed control and PLC-based systems
    Familiarity with equipment and facilities validation
    Proficient in Microsoft Office Suite.
    Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
    ~ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/visioninsurance and 401(k) to eligible employees.
    This job is eligible to participate in our short-term incentive programs.

    AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.

    It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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