Jobs and Careers
RE

Manufacturing Technician II-Packaging (nights)

Resilience
West Chester, United Statesfull_timeVerifiedPosted 20 Sept 2024
💰 $60,000/yr($42,000/yr$60,000/yr)

About the role

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 www.resilience.com

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 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.

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 detail. Capable of keeping accurate records and performing mathematical calculations.
  • Able to 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 department
  • Ability to work effectively in a team environment
  • Candidate should possess the ability to work in and adapt to a changing/demanding environment

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Resilience

View company profile →