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. ...