Biopharmaceutical Manufacturing Supervisor

Warker LLC; Portsmouth (NH); Presencial; USD 85.000 - 105.000; Jornada completa

Descripción de la vacante

Warker LLC in Portsmouth, NH seeks a Nights Manufacturing Supervisor to lead night-shift biopharmaceutical production. You will supervise manufacturing technicians, oversee batch execution, and ensure adherence to cGMP procedures in a highly regulated environment.

The role requires strong leadership, collaboration with QA, EHS, Engineering, and Supply Chain, plus proactive problem-solving to optimize yield, throughput, and right-first-time performance.

Formación

• Strong leadership experience in a regulated manufacturing setting.
• Working knowledge of cGMP, quality systems, and EHS requirements.
• Ability to analyze production performance and resolve batch-related issues.
• Strong collaboration skills with cross-functional teams.
• Commitment to patient-centric, science-driven operations and continuous improvement.

Responsabilidades

• Lead night shift manufacturing technicians and develop the team.
• Oversee batch execution and ensure adherence to cGMP procedures.
• Monitor production performance and support investigations.
• Troubleshoot operational issues and partner with QA, Engineering, and Supply Chain.
• Drive continuous improvement to enhance yield, throughput, and right-first-time performance.
• Ensure documentation and quality/EHS compliance across activities.

Conocimientos

Leadership

cGMP knowledge

Quality systems

EHS requirements

Root cause analysis

Cross-functional collaboration

Continuous improvement

Descripción del empleo

Nights Manufacturing Supervisor to lead night-shift operations in a cGMP biopharmaceutical manufacturing environment. Responsible for ensuring safe, compliant, and efficient production of therapies, while upholding Quality and EHS standards.

Key Duties

• Supervise and develop a team of manufacturing technicians
• Oversee batch execution and ensure adherence to cGMP procedures
• Monitor production performance and support investigations
• Troubleshoot operational issues and partner with QA, Engineering, and Supply Chain
• Drive continuous improvement to enhance yield, throughput, and right-first-time performance
• Ensure documentation and quality/EHS compliance across activities

Qualifications & Skills

• Strong leadership experience in a regulated manufacturing setting
• Working knowledge of cGMP, quality systems, and EHS requirements
• Ability to analyze production performance and resolve batch-related issues
• Strong collaboration skills with cross-functional teams
• Commitment to patient-centric, science-driven operations and continuous improvement