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Manufacturing Technician II

Job in Olde West Chester, West Chester Township, Butler County, Ohio, USA
Listing for: BioSpace
Full Time position
Listed on 2026-01-07
Job specializations:
  • Manufacturing / Production
    Manufacturing Production
Job Description & How to Apply Below
Location: Olde West Chester

Join to apply for the Manufacturing Technician II role at Bio Space

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.

Job Responsibilities
  • Perform the duties of operating assigned machinery, consisting of servicing machines with materials, monitoring equipment status, reintroducing materials, manually palletizing finished materials, and assuring a smooth flow of product.
  • Be able to start‑up machinery including equipment up, perform recipe selection and data entry on the 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 needed to safely move, store or deliver material to the proper location.
  • Perform visual quality inspection and sampling of in‑process materials. Promptly escalated 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, including 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 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 graduate, vocational school graduate or equivalent.
  • Working knowledge of Microsoft applications and SAP.
  • Prior production experience.
  • Experience working in a LEAN…
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