Manufacturing Technician

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. #J-18808-Ljbffr Hydrogen Group