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Packaging Technician

Job in Olde West Chester, West Chester Township, Butler County, Ohio, USA
Listing for: jobs.frontdoordefense.com - Jobboard
Full Time position
Listed on 2026-09-18
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Production QC/QA, Production Associate / Production Line, Quality Engineering
Salary/Wage Range or Industry Benchmark: 21.5 - 30.5 USD Hourly USD 21.50 30.50 HOUR
Job Description & How to Apply Below
Location: Olde West Chester

Packaging Technician

Location:

West Chester, Ohio, United States

Compensation: $21.50-$30.50 USD per hour

Job Tags:
Hardware

About

The Role

The Packaging Technician is a direct labor position reporting to a Manager/Supervisor 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.

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 elevate 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.
Other Responsibilities
  • 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 department as needed.
  • Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee as needed.
Minimum Requirements
  • Experience in a pharmaceutical or cGMP regulated environment
  • Able to effectively understand, read, write, communicate and follow instructions in the English language.
  • Good attention to…
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