Night Shift GMP Manufacturing Supervisor

Ardena; New Jersey; Sur place; USD 90 000 - 100 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Flexible working

International environment

Professional development

Meaningful work

CARE culture

Résumé du poste

Ardena Somerset, NJ is seeking a 3rd Shift Supervisor to lead 24/5 pharmaceutical manufacturing operations, ensuring GMP compliance and safe, efficient production of drug substances and products.

You will supervise production staff, manage batch records and equipment logs, and collaborate with Quality Assurance, Regulatory Affairs, and Project Management to drive continuous improvement on cGMP processes.

Qualifications

• Bachelor's Degree in Engineering, Chemistry, Mathematics, Physics, or related scientific discipline.
• 1+ years in GMP-regulated manufacturing; leadership experience preferred.
• OR Associate Degree with 4+ years in GMP manufacturing and 2+ years leadership.

Responsabilités

• Supervise daily manufacturing and packaging operations per cGMP, FDA, DEA, OSHA requirements.
• Lead, coach, and develop production staff across shifts.
• Coordinate staffing, training, performance management, and scheduling.
• Troubleshoot equipment issues and support problem solving.
• Ensure accurate batch records, equipment logs, and material reconciliation.

Connaissances

Leadership

GMP knowledge

Communication

Problem solving

ERP/QMS experience

Formation

Bachelors degree in engineering/chemistry/physics/math

Associate degree + 4+ years experience

Outils

ERP systems (e.g., Business Central)

QMS systems (e.g., MasterControl)

Microsoft Office

Description du poste

Ardena Somerset, NJ is seeking a 3rd Shift Supervisor to lead 24/5 pharmaceutical manufacturing operations, ensuring GMP compliance and safe, efficient production of drug substances and products.

You will supervise production staff, manage batch records and equipment logs, and collaborate with Quality Assurance, Regulatory Affairs, and Project Management to drive continuous improvement on cGMP processes.