Manufacturing Technician II - Packaging Line ; Night
Listed on 2026-01-15
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Manufacturing / Production
Manufacturing Production, Quality Engineering
Location: West Chester
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
Manufacturing Technician II (Packaging. Night Shift. 2/2/3 Schedule)
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
This position will require working in various Controlled/Non-Classified areas. The Packaging Technicianperforms a variety of manufacturing tasks (operates equipment, performs in-process monitoring, lineclearances, cosmetic inspection, cleaning and completes batch record entries) and supports improvement activities (5S, participate in problem-solving and Kaizen events, manual data collection) to achieve aprescribed level of purity, quality, and consistency in product and work output in accordance with cGMPs.
Job Responsibilities
* Perform the duties of operating assigned machinery consisting of servicing machines with materials, monitoring equipment status, reintroduction of materials, manually palletizing finishedmaterials, and assuring a smooth flow of product.
* Be able to start-up machinery including equipment set-up, perform recipe selection and data entry on manufacturing computerized system (SCADA and HMI), make minor adjustments, and perform critical sensor challenges.
* Perform manual packaging tasks as required including hand packaging and rework of in-processand finished material.
* Operate light material handling equipment (motorized and manual pallet jacks, non-motorizedlifts) as the need arises to safely move, store or deliver material to the proper location.
* Perform visual quality inspection and sampling of in-process materials. Promptly escalateconcerns to Lead and Process Facilitator as needed.
* Perform minor troubleshooting including clearing minor jams and identifying equipment defects.
* Work collaboratively with technical resources to resolve equipment issues as needed.
* Perform inventory control and reconciliation activities, which may require the use of SAP andWES in a limited role.
* Perform cleaning, housekeeping and line clearance activities for assigned areas to maintain acGMP environment. This includes assembling, disassembling, and sanitizing various packagingequipment.
* Perform batch record and GMP documentation entries. Perform mathematical computation asneeded.
* Be familiar with job-related safety procedures and hazards including PPEs, ergonomics, LOTO,human safety, material handling, chemical handling, and spill controls. Report all discrepancies to process facilitator.
* Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety and quality procedures.
* Support lean activities and process improvement work such as performing 5S in the work area,participating in problem-solving, and manual tracking of performance data for OEE and processimprovement analysis.
* Act as a certified OJT trainer on the team on assigned equipment and process tasks. Train and conduct evaluations on other team members for training qualifications.
* Review process documents such as operational SOPs, forms, and batch records for accuracy.
* Identify and provide suggestions for process improvement while maintaining quality and cGMP compliance as opportunities arise.
* Execute protocols as required as a part of equipment qualification and process validation work.
* Be flexible and support other work areas within the Manufacturing Team as needed.
* Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee as needed.
* Acquire and maintain all required certifications and qualifications for the assigned work area.
* Capable and motivated to learn new skills and develop new capabilities on an on-going basis to contribute to the success of the Process Execution Team.
* Ability to work effectively in a team environment.
* Candidate should possess the ability to work in and adapt to a changing/demanding environment.
* Some overtime may be required with minimal advance notice to support business needs.
Minimum Requirements
* Experience in a pharmaceutical or cGMP regulated environment
* Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language
* Good attention to detail is required. Individual must be capable of keeping accurate records and performing mathematical calculations
Preferred Background
* High school…
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