Quality Technician II; Night Shift

A career at Resilience is more than just a job - it's an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

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This Quality Technician II autonomously performs tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Class 100 aseptic environment and in a laboratory setting. This position autonomously performs tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Class 100 aseptic environment and in a laboratory setting.

• Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts from technical documentation
• Maintain accurate and complete records (i.e., laboratory notebooks, quality records, and sample receipts)
• Complete required training
• Perform visual inspections
• Use the Environmental Monitoring System to collect and analyze samples
• Guide others on SOPs (Standard Operating Procedures), control documents, and/or other work instructions. Coordinate activities of support groups
• Ensure that others carry out laboratory duties in a manner consistent with cGMP
• Perform regular audits of SOPs (Standard Operating Procedures) and/or work instructions
• Perform routine sampling activities and associated data entry
• Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities
• Read and interpret diagrams, drawings, and other schematics
• Recommend and initiate activities to ensure area and equipment is maintained in a state of compliance
• Provide feedback on service and quality issues on a timely basis

• 6pm - 6:30am
• 2/2/3 Schedule (12-Hour Rotating)

• Prior experience in a pharmaceutical production environment
• Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language
• Thorough attention to detail is required
• Must be capable of keeping accurate records and performing mathematical calculations

• High school graduate, vocational school graduate, or equivalent
• Working knowledge of MODA, Microsoft applications, SAP, KRONOS
• Experience working in a LEAN manufacturing environment