**12 hour night shift** 2-2-3 schedule. Working M-Tue, F-Su one week, then W-Th the following week

The Manufacturing Supervisor is a leader for the Inspection operation team. In this capacity, the Supervisor manages the Process / Inspection Operation to produce high quality product in accordance with the PET operating strategy. As a responsible leader for the operation (potentially with other Supervisors/Managers), this must be done while maintaining effective employee relations and compliance to cGMP, other regulatory, and SOX requirements, as well as EHS obligations and Resilience standards.

Responsibilities Include:

• Provides direction to PET personnel in the efficient use of equipment and materials to produce quality products in accordance with the PET Plan
• Responsible for all PET activity to include coordination of support staff, scheduling and improvement.
• Promotes the use of safe work practices during all aspects of production and ensures all external and Resilience SHE standards are met daily.
• Accountable for training of PET personnel on equipment, processes and Standard Operating Procedures. Partners with Process Lead to develop training plans and assist in providing resources for training.
• Ensures that cGMP’s are used and followed during production of products so that all FDA and international regulations are met. Responds to internal audit observations.
• Promotes a positive work environment by effectively administering Resilience Human Resources policies and procedures including Performance Management and by communicating information to employees and responding to their concerns.
• Ensures proper documentation practices are maintained consistently to company standards in manufacturing documents, training documentation, production logs and so on.
• Generates reports for deviations, assists in the investigations, and recommends/implements solutions to resolve deviations. Approves deviation investigations as appropriate. Responds to product defect notifications.
• Authors, reviews, and approves Standard Operating Procedures and other documents to ensure integration of cGMPs and improve process efficiencies.
• Promotes and encourages continuous improvement in efficiency, quality, production, and safety using team driven processes and key performance indicators and recognition and rewarding high performance.
• Collaborates with PET Engineers to optimize process performance.
• Participates in the design, selection, installation and qualification of new equipment, facilities, and processes.
• Reviews, approves, and implements change control.
• Provides career development and performance management for direct reports.

Minimum Qualifications:

• Experience as a leader in a production environment
• Strong communication and leadership skills
• Problem Solving Skills

Preferred Qualifications:

• Minimum 5 years of experience in GMP production environment
• Experience working in a LEAN manufacturing environment
• Working knowledge of EQV, Microsoft applications and SAP
• Training or experience in formulation, filling, inspection, packaging, validation, technology transfer, change control.
• Knowledge or previous experience in managing technical programs/projects
• Strong mechanical, electrical, troubleshooting and problem-solving abilities.
• Ability to direct and participate in cross-functional team.
• Project Management skills
• Bachelor of Science in Engineering, Pharmacy, related science or business