Manufacturing Technician

LOCATION:

Minnetonka, MN – Onsite

SCHEDULE:

2nd Shift – 4:30 PM to 3:00 AM, Monday through Thursday

DURATION: 3-Month Contract

PAY: 20-25 USD per hour

In this role, you will support GMP manufacturing and packaging activities for pharmaceutical products at the Antares Pharma Minnesota Operations Facility (APMOF).

Key responsibilities include:

• Performing routine manufacturing and packaging activities in accordance with current Good Manufacturing Practices (cGMP).
• Supporting the assembly, final packaging, and inspection of pharmaceutical products.
• Operating manual and automated manufacturing equipment while following established procedures and quality requirements.
• Maintaining accurate documentation and ensuring product traceability in accordance with Good Documentation Practices (GDP) and cGMP requirements.
• Supporting material flow throughout the production area to maintain uninterrupted manufacturing operations.
• Following all applicable company policies, Standard Operating Procedures (SOPs), Work Instructions (WIs), environmental, health, safety, and quality requirements.

• Receive and distribute materials and supplies within the manufacturing area.
• Assemble pharmaceutical products according to current SOPs and WIs while meeting established manufacturing goals and performance metrics.
• Perform final packaging and inspection activities for manufactured pharmaceutical products.
• Move materials and assembled devices within the Production area.
• Maintain uninterrupted loading and unloading of materials and assembled devices from multiple stations within automated assembly processes.
• Operate and interact with automated manufacturing equipment, including performing basic fault resets and monitoring material inputs and outputs.
• Enter equipment setup and production run information accurately.
• Ensure the quality of products and production documentation by adhering to all manufacturing processes and quality requirements.
• Complete all assigned training requirements within established timelines.
• Maintain accurate shop floor paperwork, training records, and other required documentation in accordance with GDP and cGMP guidelines.
• Follow all environmental, health, safety, and company requirements while performing production activities.
• Work effectively both independently and as part of a team in a fast-paced manufacturing environment.
• Perform other duties as assigned.

• Strong attention to detail and commitment to product quality.
• Understanding of the importance of documentation, data integrity, and product traceability.
• Familiarity with Standard Operating Procedures (SOPs) and Work Instructions (WIs) in a manufacturing or assembly environment.
• Working knowledge of Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) preferred.
• Ability to work safely and responsibly in a fast-paced manufacturing environment.
• Basic computer skills, including Microsoft 365.
• Ability to work effectively independently and within a team environment.
• Strong verbal and written communication skills.
• Strong organizational and multitasking abilities.
• Ability to follow detailed procedures and consistently meet manufacturing and quality requirements.
• Ability to work in a controlled or clean room environment requiring special gowning.
• Ability to perform physical activities including standing for extended periods, walking, and working with hands.
• Ability to lift and move materials weighing up to 30 lbs., as required.

• High School Diploma or equivalent required.
• Minimum of 1 year of experience in a medical device and/or pharmaceutical manufacturing environment.
• Equivalent combination of education and relevant experience may be…