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Production Team Leader
2 months ago
This position offers an exciting chance to contribute to a dynamic plasma manufacturing organization during the night shift. The working hours are from 6:00 pm to 6:00 am, with a rotating schedule that allows for every other weekend off.
Key Responsibilities
- Lead, guide, and mentor Technicians, Operators, and Associates within their respective roles.
- Organize and allocate workload for the shift, ensuring seamless transitions between shifts.
- Initiate Incident Notifications and engage in Failure Mode Analysis as required.
- Verify that all production materials and Personal Protective Equipment (PPE) are available as needed.
- Ensure that all team members receive effective and consistent training, adhering to cGMP and Standard Operating Procedures (SOPs).
- Develop and update SOPs and specifications as necessary.
- Champion a safe working environment; actively participate in safety teams and utilize safety metrics for continuous improvement; conduct accident investigations as needed.
- Guarantee compliance with all cGMP requirements, including batch record reviews.
- Ensure adherence to all regulations affecting manufacturing operations.
- Oversee the performance management process for direct reports, including regular reviews, coaching, and disciplinary actions when necessary; manage and resolve conflicts.
- Engage with external associations and regulatory groups as per established guidelines.
- Effectively manage conflict situations.
- Participate in recruitment efforts to maintain appropriate staffing levels within the department.
- Maintain a clean and organized work area in accordance with cGMP and internal standards.
- Keep the work area in a state of readiness for Environmental Health & Safety (EH&S) and GMP regulatory audits at all times.
- Perform additional duties as assigned.
Qualifications and Experience:
- A Bachelor's Degree in Science, Engineering, or a related field is required.
- A minimum of five (5) years of experience in a manufacturing setting, with at least three (3) years in a supervisory capacity.
- Familiarity with the Fractionation Process is advantageous.
- Proficiency in Microsoft Office Suite, Microsoft Project, and database management is preferred.
- Comprehensive knowledge of global cGMPs, regulations, and validation requirements is essential.