Night Shift GMP Manufacturing Supervisor

Ardena

New Jersey

On-site

USD 90,000 - 100,000

Full time

14 days+

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Benefits offered by this job

Competitive salary
Flexible working
International environment
Professional development
Meaningful work
CARE culture

Job summary

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.

Responsibilities

  • 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.

Skills

Leadership
GMP knowledge
Communication
Problem solving
ERP/QMS experience

Education

Bachelors degree in engineering/chemistry/physics/math
Associate degree + 4+ years experience

Tools

ERP systems (e.g., Business Central)
QMS systems (e.g., MasterControl)
Microsoft Office

Job description

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.

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