Supervisor, Visual Inspection; Nights

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The Supervisor, Visual Inspection is a leader for the Process Operation (Inspection). In this capacity, the Supervisor manages the Visual 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 HSE obligations and Resilience standards.

• Provides direction to PET staff in the efficient use of equipment and materials to produce quality products in accordance with the PET Plan or Rhythm Wheel.
• Responsible for all PET activity, including 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 HSE standards are met daily.
• Accountable for training of PET staff on equipment, processes and Standard Operating Procedures.
• Ensures that cGMPs are used and followed during production of products so that all FDA and international regulations are met. Responds to monthly internal audit observations.
• Promotes a positive work environment by effectively administering people 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 OE Engineers & 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.
• Co‑owns life cycle management of PET/facility assets.
• Works collaboratively within and across PETs to ensure flow of product, sharing of best practices and lean behaviors.
• Maintains presence across multiple operating shifts.
• Occasionally performs rolls for PET Lead when designated.

• Previous experience in GMP production environment.
• Strong communication and leadership skills.
• Problem solving skills.
• Ability to direct and participate in cross-functional team.
• Knowledge or previous experience in managing technical programs/projects.
• Strong mechanical, electrical, troubleshooting and problem‑solving abilities.

• Bachelor of Science in Engineering, Pharmacy, related Science or business.
• Experience working in a LEAN manufacturing environment.
• Working knowledge of LDMS, Microsoft applications, SAP, Trackwise.
• Training or experience in formulation, filling, packaging, validation, technology transfer, change control.
• Project management skills.

Sponsorship or support for work authorization, including visas, is not available for this position.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age,…