NEW JOB OPENING
PRODUCTION GROUP LEAD
IN Minnetonka, MN, USA!

 

Date Posted: 05/14/2026
Hiring Organization: Rose International
Position Number: 501240
Industry: Pharmaceutical/Healthcare
Job Title: Production Group Lead
Job Location: Minnetonka, MN, USA, 55345
Work Model: Onsite
Shift: Monday to Thursday, 3 PM to 4:30 AM (OT as needed during the week and on Fridays)
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 12
Min Hourly Rate($): 27.50
Max Hourly Rate($): 27.50
Must Have Skills/Attributes: Manufacturing, Medical device, Production Support
Experience Desired: Production Manufacturing Leadership (4-6 yrs); Background in medical device, pharmaceutical, or regulated manufacturing environments (4-6 yrs)
Required Minimum Education: High School Diploma or equivalent

**C2C is not available**

 

Job Description
Education:

• High School Diploma or Equivalent



Qualifications

• Experience in manufacturing, production coordination, or manufacturing leadership roles

• Background in medical device, pharmaceutical, or regulated manufacturing environments preferred

• Knowledge of FDA regulations, quality systems, and manufacturing compliance standards

• Experience with operator training, process audits, and production support activities

• Familiarity with lean manufacturing, 5S, preventive maintenance, and continuous improvement initiatives

• Strong communication, organizational, and problem-solving skills

• Ability to work effectively in a fast-paced team environment



Manufacturing Group Lead – Medical Device Operations

We are seeking a motivated Manufacturing Group Lead to support daily production operations within a regulated medical device manufacturing environment. This role is responsible for coordinating production activities, supporting manufacturing operators, ensuring quality and compliance standards are met, and contributing to continuous improvement initiatives. The ideal candidate will bring strong manufacturing experience, leadership abilities, and a proactive approach to problem-solving in a fast-paced production environment.



Key Responsibilities

• Coordinate daily production activities to ensure products are processed according to build schedules and operational priorities

• Communicate work instructions and production updates to manufacturing personnel

• Monitor production and quality performance to ensure operational goals are achieved

• Perform process and quality audits for personnel, equipment, and tooling

• Support troubleshooting activities and escalate equipment or production issues when necessary

• Assist with operator training, retraining, and performance support

• Review defects, support disposition activities, and maintain accurate production documentation

• Participate in daily production meetings and continuous improvement initiatives

• Support preventive maintenance and calibration tracking activities

• Coordinate purchase requests for equipment and operational services

• Maintain compliance with FDA regulations, quality systems, environmental standards, and company procedures

• Collaborate with cross-functional teams including production, quality, engineering, maintenance, and operations
  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**


 

Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

 

Apply Now

Send me a reminder to complete this application
Apply Now

 

About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

Rose International has been great to me. I thank everyone there for all of their hard work; it has not gone unnoticed.

Melody, Consultant

Rose International maintained good communication during assignments and are very informative through email and phone calls.

Sade, Consultant

Each time I contacted Rose, I was completely satisfied with the great attention and customer service I received. Each person was extremely knowledgeable and patient with my concerns or questions.

Diana, Consultant

Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.

Diane, Consultant

I am very happy with the Rose International, and the professionalism of the employees.

Robin, Consultant

EMPLOYEE COMMENTS

  • We want you to work with us, but don't take our word for it. Take a look at this sampling of employee comments. They speak for themselves.