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Manufacturing Technician II, Packaging; Nights

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 (Nights)
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

Brief Job Description

The Packaging Technician II is a direct labor position reporting to a Process Execution Team Process Facilitator on the Manufacturing floor, which supports Packaging operations. This position will require working in various Controlled/Non-Classified areas. The Packaging Technician performs a variety of manufacturing tasks (operates equipment, performs in-process monitoring, line clearances, 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 a prescribed level of purity, quality, and consistency in product and work output in accordance with cGMPs.


** This a Nigh Shift position working 6pm - 6:30am. 2 days on, 2 days off, 3 days on, 3 days off and the rotation starts over again.

Primary Responsibilities

  • Perform the duties of operating assigned machinery consisting of servicing machines with materials, monitoring equipment status, reintroduction of materials, manually palletizing finished materials, 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-process and finished material.

  • Operate light material handling equipment (motorized and manual pallet jacks, non-motorized lifts) 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 escalate concerns 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 and WES in a limited role.

  • Perform cleaning, housekeeping and line clearance activities for assigned areas to maintain a cGMP environment. This includes assembling, disassembling and sanitizing various packaging equipment.

  • Perform batch record and GMP documentation entries. Perform mathematical computation as needed.

  • 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 process improvement 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 Process Execution Team as needed

  • Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee as needed.

Minimum Qualifications

  • Acquire and maintain all required certifications and qualifications for the assigned work area

  • Experience in a pharmaceutical or cGMP regulated environment

  • Capabl…

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