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Resilience

Biologics and sterile injectables CDMO

Manufacturing Supervisor - Multiple Teams

Machine & Process OperationConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USAIn-person

About the Job

Requirements

  • Prior experience in a production environment.
  • Previous leadership experience leading direct reports.
  • Communication and leadership skills.
  • Problem-solving skills.
  • Demonstrated understanding of how technical documentation, including standard operating procedures, batch records, and work instructions, is written and used in a production environment.
  • Ability to demonstrate and maintain gown qualification standards.

Responsibilities

  • Provide direction to Process Execution Team personnel in the efficient use of equipment and materials to produce quality products in accordance with regulations.
  • Be responsible for all Process Execution Team activity, including coordination of support staff, scheduling, and improvement.
  • Promote safe work practices during all aspects of production and ensure all external and internal environmental, health, and safety standards are met daily.
  • Train Process Execution Team personnel on equipment, processes, and standard operating procedures; partner with the Process Execution Team Coach to develop training plans and assist in providing training resources.
  • Ensure current good manufacturing practices are followed during production so that applicable Food and Drug Administration and international regulations are met, and respond to monthly internal audit observations.
  • Administer Human Resources policies and procedures, including performance management, communicate information to employees, and respond to employee concerns.
  • Ensure consistent documentation practices in manufacturing documents, training documentation, production logs, and other records.
  • Generate deviation reports, assist with investigations, recommend and implement solutions, approve deviation investigations as appropriate, and respond to product defect notifications.
  • Author, review, and approve standard operating procedures and other documents to integrate current good manufacturing practices and improve process efficiencies.
  • Promote continuous improvement in efficiency, quality, production, and safety using team-driven processes, key performance indicators, and recognition and rewards for high performance.
  • Collaborate with Operational Excellence Engineers and Process Execution Team Engineers to optimize process performance.
  • Participate in the design, selection, installation, and qualification of new equipment, facilities, and processes.
  • Provide career development and performance management for direct reports.
  • Collaborate within and across Process Execution Teams to ensure product flow and share best practices and lean behaviors.
  • Maintain a presence across multiple shifts.
  • Occasionally perform Process Execution Team Lead duties when designated.

Desired Qualifications

  • Bachelor of Science in Engineering, Pharmacy, a related Science field, or Business.
  • Experience working in a lean manufacturing environment.
  • Working knowledge of Learning Document Management System or Veeva, Microsoft applications, and SAP.
  • Experience working in SAP, particularly with production orders, inventory movements, and confirmations related to filling operations.
  • Training or experience in formulation, filling, packaging, validation, technology transfer, or change control.
  • Knowledge of or previous experience with pharmaceutical manufacturing; aseptic filling experience is preferred.
  • Strong mechanical, troubleshooting, and problem-solving abilities.
  • Ability to direct and participate in cross-functional teams.
  • Project management skills.
  • Ability to work effectively in a team environment.
  • Ability to work effectively in a changing or demanding environment.

About the Company

Resilience

Biologics and sterile injectables CDMO

Resilience is a North American CDMO focused on biologics and sterile drug products. It provides end-to-end services from development through commercial production, including biologics development and drug substance manufacturing, aseptic fill/finish, device assembly, packaging, logistics, regulatory support, and tech transfer, all coordinated via a stage-gate process and a digital quality management system. It differentiates itself with North American-based, integrated biologics and sterile capabilities, a focus on sterile injectables and device assembly, and recent expansion into injectable pen devices for diabetes and obesity medicines. Its goal is to broaden access to complex medicines while protecting North American biopharma supply chains with dependable capacity and strong regulatory support from clinical development to commercial scale.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$3.2B
Headquarters
Blue Ash, OH
Founded
2020

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