Manufacturing Supervisor

4 weeks ago

Melville, United States Kedrion Biopharma Full time

This is a great opportunity to work for a growing plasma manufacturing company on the night shift . Hours are 6:00 pm - 6:00 am. Week one: scheduled work days will be Mon, Tues, Fri, Sat & Sun and week two: scheduled work days will be Wed & Thurs allowing you to have off every other weekend.



Main Responsibilities

  • Provide leadership, direction and mentoring to Technicians/Operators/Associates in their respective work environments.
  • Schedules workload for shift and assures a smooth and timely transition between shifts.
  • Initiates Incident Notifications and conducts and participates in Failure Mode Analysis as necessary.
  • Ensure all production materials and PPE are present as required.
  • Ensures all employees are trained effectively and consistently and comply with cGMP’s and SOPs.
  • Develop SOP’s and specifications as required.
  • Provide leadership to ensure a safe work environment; Participate in company-wide safety teams, utilizing safety metrics and goals for improvement; Conducts and participates in accident investigations as necessary.
  • Ensure compliance with all cGMP requirements, including batch record review.
  • Ensure compliance with all regulations impact the manufacturing operations
  • Responsible for managing the performance management process of the direct reports including periodic written reviews, coaching, and disciplinary action if required. Manages and resolves conflicts
  • Participates with outside associations and/or regulatory groups within established guidelines.
  • Satisfactorily handles conflict situations
  • Participate in hiring as required to maintain appropriate staffing levels in the department.
  • Ensures the work area is maintained in a clean an orderly manner in accordance with cGMP and internal requirements;
  • Must keep the work area in EH&S / GMP regulatory audit ready conditions at all times;
  • Additional duties as assigned.


Background and Experience:

  • Bachelor's Degree in Science, Engineering, or related field required.
  • Five (5) years’ experience in a manufacturing environment with a minimum of three (3) years in a supervisory role.
  • Knowledge of Fractionation Process a Plus
  • Knowledge of Microsoft Office Suite, Microsoft Project, and Database management preferred.
  • Extensive knowledge of global cGMPs, regulations and validation requirements.

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