Shift Production Supervisor - cGMP CBD Manufacturing

Big Sky Scientific

Sun River (MT)

On-site

USD 55,000 - 85,000

Full time

14 days+

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Job summary

Big Sky Scientific in Sun River, MT is seeking a Production Shift Supervisor to oversee daily extraction and refinement operations on-site. You will lead a production team, coordinate schedules, and ensure processes run safely and in compliance with cGMP and FDA guidelines.

Responsibilities include coaching staff, monitoring equipment and materials, documenting production data, and collaborating with management and quality teams to support continuous improvement and consistent output targets.

Qualifications

  • Minimum high school diploma or equivalent; technical or supervisory training is a plus.
  • Demonstrated ability to lead a production team and coordinate shift activities.
  • Experience with production schedules and planning to meet output targets.
  • Strong skills in production management, resource allocation, and process monitoring.
  • Excellent communication for instructions, reporting, and cross-department collaboration.
  • Familiarity with cGMP practices or FDA-regulated environments preferred.
  • Ability to stand for extended periods in a production setting and follow safety protocols.
  • Experience in manufacturing, food processing, pharmaceuticals, or related industries is beneficial.

Responsibilities

  • Oversee daily production activities to ensure safe, compliant operations.
  • Lead and coach production staff, assign tasks, and monitor workflow.
  • Maintain production schedules, coordinate with management on priorities.
  • Enforce safety protocols and document production data for quality records.

Skills

Supervisory Skills
Production Scheduling
Production Planning
Production Management
Communication
Safety procedures
Manufacturing experience

Education

High school diploma or equivalent

Job description

Big Sky Scientific in Sun River, MT is seeking a Production Shift Supervisor to oversee daily extraction and refinement operations on-site. You will lead a production team, coordinate schedules, and ensure processes run safely and in compliance with cGMP and FDA guidelines.

Responsibilities include coaching staff, monitoring equipment and materials, documenting production data, and collaborating with management and quality teams to support continuous improvement and consistent output targets.

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