Manufacturing Technician Contractor (SHIFT 1/2 – 6:00am to 4:30pm (Monday through Thursday)
Location: Minnetonka, Minnesota
Country: United States
Category: Clinical Development and Operations
Workplace Location: Onsite
Employment Type: Contract
Posted Date: July 6, 2026
Job ID: 649223
Job Description
Job Title: Manufacturing Technician Contractor
Location: Minnetonka, MN
Contract length: 6 months
Schedule: Fulltime, M-T, 4 - 10 hours shifts with OT available sometimes on Friday
Shift Timings: 6:00am to 4:30pm (Monday through Thursday)
Pay: $20/hr to $24/hr, DOE
Job Overview:
The Manufacturing Technician will be responsible for performing routine tasks for the GMP manufacturing and packaging of pharmaceutical products at the Antares Pharma Minnesota Operations Facility (APMOF). The successful candidate will be familiar with current Good Manufacturing Practices (cGMP). This individual is responsible for the documentation and the hands-on execution of production activities related to assembly, final packaging, and inspection of manufactured pharmaceutical products. This individual operates in accordance with Antares Pharma policies and procedures, environmental, health, safety, and cGMP guidelines.
Job Responsibilities:
- Responsible for quality of products and documentation. Adheres to all manufacturing process and quality requirements.
- Receives and distributes materials and supplies in the manufacturing area.
- Works with manual as well as automated equipment to complete assembly, final packaging, and inspection of pharmaceutical products.
- Moves materials within the Production area.
- Responsible for maintaining uninterrupted loading/unloading of materials and assembled devices from multiple stations of an automated assembly process.
- Interacts with automated equipment to perform basic fault resetting, monitoring of material inputs/outputs and entering setup/run information.
- Completes assigned training prior to due dates.
- Assembles products following all current Standard Operating Procedures (SOPS) and Work Instructions (WIs), while meeting manufacturing goals and metrics.
- Ability to maintain accurate records following Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) guidelines including training files and shop floor paperwork.
- Other duties as assigned
Job Qualifications:
- High School Diploma or equivalent is required.
- 1 year of experience in a medical and/or pharmaceutical manufacturing setting
- An equivalent combination of experience and education may be considered
- Must be able to work in a controlled or clean room environment requiring special gowning.
EEO Statement
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The Planet Group and our companies are equal opportunity employers. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity, and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.
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About The Planet Group
The Planet Group is a global professional services firm delivering strategic staffing and advisory solutions. We operate at the intersection of talent and transformation – connecting the right people with the right opportunities in the areas of technology, engineering, accounting & finance, digital marketing, and manufacturing.
As one of the largest staffing companies in the US, we operate with a global reach and a performance-first mindset. We partner with clients to move fast, stay agile, and drive measurable results – building high-impact teams that fuel transformation and growth.
