Manufacturing Technician II - Formulation; Nights

Job Summary

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. For more information, please visit

• The Technician operates equipment, performs in-process monitoring, line clearances, OEE data collection, and batch record entries per cGMPs.
• Perform start-up, equipment operation, batch execution, material handling, cleaning, housekeeping, and line clearance activities as required to maintain a cGMP environment.
• Work collaboratively with mechanic technicians and lead technicians to resolve production-related issues such as batch set-up, execution, documentation, equipment operations, SOPs, and safety and quality inspection procedures.
• Monitor process execution, material, and supply levels to ensure successful operations on the production floor; coordinate production tasks such as batch execution.
• Perform clean in place and steam in place of process lines per SOPs.
• Perform, set up, and create single-use connections including single-use bags.
• Perform and execute filter integrity testing as needed per SOP.
• Perform parts washing and dispensing operations as necessary.
• Assemble, disassemble, and sanitize equipment.
• Operate automated and semi-automated equipment (pumps, mixers, etc.).
• Assist technical staff with preventive maintenance procedures as required.
• Support lean activities including 5S, problem-solving, process improvement analysis, and manual tracking of performance data for OEE data tracking.
• Perform inventory control using SAP.

• Acquire and maintain all required certifications and qualifications for the assigned work area.
• Cross-train and support other work areas as needed.
• Attend and actively participate in daily tier meetings.

• Prior experience in a regulated manufacturing environment.
• Working knowledge of automated and semi-automated equipment (pumps, mixers, etc.) as well as light material handling equipment.
• Ability to effectively read, write, speak, and understand English to follow detailed instructions and communicate with team members.
• Demonstrated attention to detail with the ability to accurately complete batch records, logbooks, and other controlled documentation.
• Basic problem solving and mathematical skills, including the ability to perform routine calculations (e.g., weights, measures, conversions).
• Ability to follow SOPs, written procedures and work instructions with minimal supervision, escalating issues as needed.
• Ability to identify deviations or inconsistencies in processes or documentation.
• Ability to work effectively as part of a team in a fast-paced production environment.

• High school graduate, vocational school graduate, or equivalent.
• 1+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
• Working knowledge of cGMP principles, including documentation practices, safety procedures, and compliance expectations.
• Experience working in a lean manufacturing environment.
• Working knowledge of Microsoft applications, SAP and/or Veeva Vault.

This role is primarily a non-Sedentary role. This can include climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects. Visual acuity such as working with data & figures, viewing computer terminals, extensive reading, operating machinery, operating motor vehicles, general observations of facilities, etc. Participation in an…