Maintenance Technician IV - IDAP (Nights)

Resilience•Blue Ash, OH

5d•$29 - $47•Onsite

About The Position

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. The Maintenance Technician IV, DAP is responsible for performing ongoing corrective, predictive, and preventative maintenance for the process equipment within the assigned operating area. This position also could entail the execution of setup and changeover support for all process equipment used in various controlled areas up to a Controlled Not Classified (CNC) environment. It requires the ability to perform mechanical and electrical troubleshooting in order to ensure optimal operation of the process equipment. In addition, the individual will perform basic mechanical training to Production Operators and serve as a resource to help implement continuous improvement projects.

Requirements

Demonstrated experience performing corrective, preventative, and predictive maintenance on automated process equipment in a regulated GMP environment.
Demonstrated mechanical and electrical troubleshooting proficiency, including mechanics, hydraulics, pneumatics, and electronics.
Familiarity with controlled (CNC) manufacturing environment requirements, including gowning, environmental monitoring awareness, and clean room behavior.
Ability to independently diagnose and resolve equipment failures with limited supervision; makes independent decisions regarding own maintenance work.
Proficient in Computerized Maintenance Management Systems (e.g., Maximo, SAP); independently operates CMMS to create, update, and close work orders.
Demonstrated ability to complete and review GMP documentation accurately, including work orders, batch records, and maintenance logs per cGMP requirements.
Ability to read and interpret electrical schematics, mechanical drawings, and equipment manuals.
Ability to effectively understand, read, write, communicate, and follow instructions in the English language.

Nice To Haves

High school diploma or GED Associate degree or vocational/trade school certification in a relevant discipline (e.g., industrial maintenance, electrical, mechanical, instrumentation) preferred.
4+ years of experience in equipment maintenance within a regulated pharmaceutical or GMP manufacturing environment.
Experience with OEE, TPM, LEAN, or other continuous improvement methodologies.
Knowledge of data and materials systems such as Maximo, SAP, ADP, KRONOS, or other MRP/ERP systems.
Experience with automated pharmaceutical manufacturing equipment (e.g., inspection, assembly, packaging, or filling equipment).

Responsibilities

Complete emergency repair, rebuilding, changeover, and inspection work on process-related equipment.
Install, inspect, test, adjust, repair, and perform line turnarounds, changeovers, and preventative maintenance per established procedures in a timely and efficient manner.
Responsible for equipment and system performance through data monitoring within the assigned operating area.
Use a variety of testing, tools, and measuring equipment in the efficient maintenance and troubleshooting of electronic, environmental monitoring, pneumatic, hydraulic, and mechanical line equipment.
Install new equipment and oversee equipment upgrades according to site SOPs.
Perform 5S activities and maintain organization of operating areas.
Work with limited supervision, identifying and prioritizing maintenance needs within the assigned operating area in coordination with the Maintenance Facilitator, Process Facilitator, Engineer, or other activity leads.
Perform roles of Technician and Mechanical Technician as required to support daily PET activities.
Utilize appropriate Problem Solving and Troubleshooting techniques to complete equipment repairs.
Serve as a project resource to PET to assist in the follow up and timely implementation of projects and validation activities.
Perform cleaning and housekeeping activities for assigned areas as required to maintain a cGMP environment.
Complete documentation and required functions in the work order system to close out activities in compliance with cGMPs.
Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs, and established safety procedures in accordance with OSHA requirements and guidelines.
Be familiar with Material Safety Data Sheets for area chemicals.
Perform batch record and GMP documentation entries. Maintain records and/or logs as required. This will include mathematical computation where needed.
Follow and maintain compliance with established MRO procedures and inventory control.
Provide training to operators for equipment set-up and for minor adjustments or repairs.
Responsible for maintaining Gowning and controlled-environment certifications as required to support assigned work areas (area dependent).