Production Supervisor

Metric Bio; United States; On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Relocation support available

Job summary

Metric Bio is seeking a Production Supervisor for the night shift in the Midwest, responsible for overseeing GMP manufacturing operations. The ideal candidate will lead a team, ensuring safety and compliance while driving continuous improvement. Applicants should possess a Bachelor's degree in science or engineering and have 3–5 years of relevant experience in the pharmaceutical industry.

Qualifications

• Bachelor’s degree in a scientific or engineering discipline preferred (or equivalent experience).
• 3–5 years in a pharmaceutical or chemical manufacturing environment.
• Prior supervisory or team leadership experience.
• Strong knowledge of GMP and safety requirements in a batch manufacturing setting.
• Excellent communication, organizational, and problem-solving skills.

Responsibilities

• Oversee night shift API manufacturing activities, ensuring safety, compliance, and adherence to batch records.
• Supervise and develop a team of production technicians, providing training, scheduling, and performance management.
• Support investigations and deviations, and assist with CAPA implementation.
• Partner with QA, EHS, Maintenance, and Technical Services to resolve issues and support batch execution.
• Maintain accurate documentation in compliance with GMP standards.
• Monitor and report on production metrics and process performance.
• Drive continuous improvement initiatives across safety, quality, and efficiency.

Skills

GMP Compliance

Leadership

Communication

Problem-solving

Organizational Skills

Education

Bachelor’s degree in a scientific or engineering discipline

Job description

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Global CDMO & Clinical Supply Recruitment Specialist | Metric Bio

Job Title: Production Supervisor – Night Shift

Location: Midwest, US – Onsite

Relocation support is available!

About the Company

A global CDMO focused on small molecule APIs. With facilities across North America and Europe, they support clients throughout the pharmaceutical development lifecycle — from early development to commercial manufacturing — with expertise in complex and hazardous chemistry.

Position Summary

This role is responsible for supervising night shift manufacturing operations in a GMP production environment. You’ll lead a team of production technicians, ensuring safe, compliant, and efficient batch execution while supporting continuous improvement, training, and operational excellence.

This is a full-time, onsite night shift position (6:00 PM – 6:30 AM) operating on a 2-2-3 schedule — offering every other weekend off and predictable rotating days.

Key Responsibilities

• Oversee night shift API manufacturing activities, ensuring safety, compliance, and adherence to batch records
• Supervise and develop a team of production technicians, providing training, scheduling, and performance management
• Support investigations and deviations, and assist with CAPA implementation
• Partner with QA, EHS, Maintenance, and Technical Services to resolve issues and support batch execution
• Maintain accurate documentation in compliance with GMP standards
• Monitor and report on production metrics and process performance
• Drive continuous improvement initiatives across safety, quality, and efficiency

Qualifications

• Bachelor’s degree in a scientific or engineering discipline preferred (or equivalent experience)
• 3–5 years in a pharmaceutical or chemical manufacturing environment
• Prior supervisory or team leadership experience
• Strong knowledge of GMP and safety requirements in a batch manufacturing setting
• Excellent communication, organizational, and problem-solving skills

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Manufacturing, Product Management, and Production

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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