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.
