Supervisor Manufacturing Operations

Supervisor Manufacturing Operations

Contract Type:

Temporary

Location:

Minnetonka

Industry:

Manufacturing and Production

Contact Name:

Giulia Memore

Contact Phone:

Date Published:

06-May-2026

JOB TITLE: Manufacturing Operations Supervisor

LOCATION: Onsite – Minnetonka, MN

SCHEDULE: 9:00 AM – 5:00 PM

DURATION: 10-Week Contract

PAY: 47-52 USD per hour


Job Responsibilities:

In this role, you will lead and oversee daily manufacturing and packaging operations within a pharmaceutical production environment. Key responsibilities include:

  • Managing multi-shift production teams, including:

    o Supervising hourly and contract employees

    o Coaching and mentoring staff on best practices

    o Driving team engagement and performance
  • Overseeing GMP manufacturing and packaging of pharmaceutical products in a cleanroom environment
  • Promoting a culture of safety, quality, compliance, and continuous improvement
  • Coordinating with cross-functional teams (quality, engineering, product development) to ensure smooth operations
  • Monitoring production performance, schedules, and efficiency


    Essential Duties and Job Functions:

  • Ensure all manufacturing and packaging activities follow current Good Manufacturing Practices (cGMP) and internal procedures
  • Plan and coordinate cleaning, production, packaging, and documentation activities to maximize efficiency
  • Lead daily production operations and track performance against established metrics
  • Identify manufacturing issues, perform root cause analysis, and implement corrective actions
  • Review batch records and documentation as a subject matter expert
  • Communicate production updates and performance to leadership
  • Manage, coach, and develop manufacturing technicians through training and mentorship
  • Monitor and ensure completion of required training for all team members
  • Create, update, and maintain technical documents using change control systems
  • Support administrative functions such as performance reviews, hiring, and disciplinary actions
  • Drive continuous improvement initiatives using Lean Manufacturing principles
  • Ensure adherence to safety standards and regulatory compliance


    Knowledge & Skills:

  • Strong understanding of cGMP and Good Documentation Practices (GDP)
  • Experience in pharmaceutical or medical device manufacturing environments
  • Knowledge of Lean Manufacturing principles and continuous improvement practices
  • Strong leadership, coaching, and team management skills
  • Ability to perform root cause analysis and implement effective solutions
  • Experience with technical writing and documentation systems
  • Proficiency in Microsoft Office applications
  • Strong organizational, multitasking, and problem-solving skills
  • Effective communication skills with ability to adapt to different audiences
  • Ability to work in a fast-paced, regulated production environment


    Education & Experience:

  • High School Diploma or equivalent with 5–8 years of manufacturing experience (pharmaceutical or medical device preferred), OR
  • Associate’s Degree with relevant experience
  • Experience supervising or leading teams in a production environment
  • Demonstrated experience in employee training and development
  • Experience in cleanroom and GMP-regulated environments preferred


    Additional Requirements:

  • Ability to stand for extended periods, walk, and perform physical tasks (including lifting up to 30 lbs)
  • Comfortable working in a manufacturing and/or laboratory environment
  • Travel may be required up to 5%

...

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