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    Production Supervisor, 2nd/3rd shift - Chantilly, United States - Granules Pharmaceuticals

    Granules Pharmaceuticals
    Granules Pharmaceuticals Chantilly, United States

    1 week ago

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    Description


    Job Title: Production Supervisor at Pharmaceutical Company

    The Production Supervisor is in charge of coordinating and organizing the daily work schedules for both employees and equipment in the Production line.

    • Responsible for overseeing operators involved in Granulation, Drying, Blending, Compression, Pellet coating, Tablets coating, and Encapsulation of various drug products.
    • Must ensure compliance with department quality, safety, delivery, and productivity targets for Granules branded products, developmental items, generic drugs, and contract customer products.
    • Proficiency in cGMPs and good manufacturing practices; must possess excellent communication, teaching, and motivational skills to drive team performance.

    The role involves extensive documentation, investigative writing, production planning, and labor management skills. Additionally, responsibilities include reviewing and approving batch record documentation, executing yield transactions, and ensuring adherence to Good Manufacturing Practices and company procedures.

    Key Responsibilities:

    • Overseeing hourly operators to ensure compliance with validated parameters and standard operating procedures.
    • Developing daily/weekly work schedules, setting priorities, and confirming resource availability.
    • Reviewing batch records and supporting documents before submission to Quality.
    • Leading investigations for cause, defining corrective actions, writing reports, and ensuring timely closure.
    • Initiating change control assignments for continuous process improvement.
    • Conducting and overseeing operator training programs on SOPs, cGMP, and safety.
    • Participating in safety meetings and accident investigations, implementing corrective actions.
    • Reporting production updates and schedule changes to the team and management.
    • Driving operational performance improvements and providing constructive feedback to union colleagues.
    • Participating in CMO audits or regulatory agency inspections.

    Requirements:

    • Minimum Education Required: B.A./B.S. Degree in Science, Business, or related field or significant experience.
    • Desired: B.A./B.S. Degree in Pharmaceutical Sciences, Business Management, or related area.
    • Minimum 5 years of supervisory experience in Pharmaceutical Manufacturing, Operations, or Quality Department.
    • Knowledge of Quality Management Systems, Document Management Systems, and MS Office Suite.
    • Understanding of current state, federal, and local standards and regulations such as cGMP, OSHA, FDA, and DEA.


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