Manufacturing Technician

The Planet Group

Minnetonka (MN)

On-site

USD 24,796 - 30,307

Full time

14 days+

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Job summary

The Planet Group is seeking a Production Associate for our pharmaceutical manufacturing operations in Minnetonka, MN. The role requires adherence to GDP/cGMP, SOPs, and work instructions while maintaining accurate documentation and quality standards.

You will work in a controlled environment, handle materials, and operate both manual and automated equipment to assemble, package, and inspect pharmaceutical products, ensuring compliance with all quality requirements.

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
  • Critical understanding of the importance of documentation and data traceability
  • Must have the ability to work safely and responsibly in a fast-paced manufacturing environment
  • Familiarity with executing Standard Operating Procedures (SOPs) in a manufacturing or assembling environment, preferably in the pharmaceutical industry

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 description

  • 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

Required 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
  • Critical understanding of the importance of documentation and data traceability
  • Must have the ability to work safely and responsibly in a fast-paced manufacturing environment
  • Familiarity with executing Standard Operating Procedures (SOPs) in a manufacturing or assembling environment, preferably in the pharmaceutical industry
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