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

Job Responsibilities:

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.

Essential Duties and Job Functions:

· 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.

Knowledge & Skills:

· 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.

Education & Experience:

· 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 considered.

· Experience working in a controlled or clean room environment preferred.

· Experience working with manufacturing or assembly equipment preferred.

· Familiarity with pharmaceutical manufacturing, GMP, GDP, and quality systems preferred.

· Experience in biology and/or chemical laboratory environments may be required, where applicable.

Environmental Conditions:

· Ability to work in a controlled or clean room environment requiring special gowning.

· Work may involve prolonged periods of standing, walking, and performing hands-on manufacturing activities.

· Some lifting and movement of materials up to 30 lbs. may be required.

· Work environment typically has low to moderate noise levels.

· Environmental health and safety requirements apply to all manufacturing and laboratory activities, as applicable.

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