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Manufacturing Technician II - Packaging Line ; Night

Job in West Chester, West Chester Township, Butler County, Ohio, USA
Listing for: Resilience
Full Time, Part Time position
Listed on 2026-01-15
Job specializations:
  • Manufacturing / Production
    Manufacturing Production, Quality Engineering
Job Description & How to Apply Below
Position: Manufacturing Technician II - Packaging Line 3 (Night)-3
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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