R

Resilience

Biologics and sterile injectables CDMO

Maintenance Technician 4 Lead - Sterile Operations

Equipment MaintenancePosted on Nov 9
Full-timeWest Chester Township, OH, USAIn-person

About the Job

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 aseptic and sterile manufacturing environment requirements, including gowning, environmental monitoring awareness, and clean room behavior.
  • Ability to independently diagnose and resolve equipment failures with limited supervision and make independent decisions regarding own maintenance work.
  • Proficiency in Computerized Maintenance Management Systems (CMMS), such as Maximo or SAP, including independently creating, updating, and closing 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 understand, read, write, communicate, and follow instructions in English.
  • Demonstrated experience coordinating team activities and taking point on shared tasks alongside other maintenance technicians in a GMP manufacturing environment, including sound operational decision-making under pressure.
  • Demonstrated ability to train other technicians on equipment setup, operation, troubleshooting, and maintenance procedures.
  • Ability to demonstrate and maintain gown qualification standards.
  • Ability to perform non-sedentary work that may include climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects.
  • Ability to use required personal protective equipment, which may include respirators, powered air-purifying respirators, gowns, gloves, face protection, and other barrier equipment.
  • Ability to adhere to the established Quality Management System, including the Quality Manual, Quality Policy, Standard Operating Procedures, current Good Manufacturing Practices, and applicable regulations and standards.

Responsibilities

  • Lead emergency repair, rebuilding, changeover, and inspection work on process-related equipment; install, inspect, test, adjust, repair, and perform line turnarounds, changeovers, and preventative maintenance according to established procedures.
  • Monitor data to ensure equipment and system performance within the assigned operating area.
  • Use testing and measuring equipment and tools to maintain and troubleshoot electronic, environmental monitoring, pneumatic, hydraulic, and mechanical line equipment.
  • Lead installation of new equipment and oversee equipment upgrades according to site standard operating procedures.
  • Lead and perform 5S activities and maintain organization of operating areas.
  • Perform Technician and Mechanical Technician duties as required to support daily PET activities.
  • Serve as a project resource to PET by following up on and implementing projects and validation activities in a timely manner.
  • Perform cleaning and housekeeping in assigned areas to maintain a cGMP environment.
  • Complete work order system documentation and required functions, and help ensure other technicians’ documentation is accurate and complete for cGMP-compliant activity closeout.
  • Perform work responsibly and reinforce compliance with standard operating procedures, cGMPs, and established safety procedures in accordance with OSHA requirements and guidelines.
  • Be familiar with Material Safety Data Sheets for area chemicals.
  • Complete batch record and GMP documentation entries, help other technicians identify errors before submission, and maintain required records and logs, including mathematical computations when needed.
  • Follow and maintain compliance with established MRO procedures and inventory control.
  • Maintain Aseptic Processing and Gowning certifications as required for assigned work areas.
  • Act as a certified on-the-job trainer for assigned equipment and process tasks; provide hands-on training to operators and Process Maintenance Technicians on equipment setup and major and minor adjustments or repairs.
  • Teach problem-solving and troubleshooting techniques for completing equipment repairs.
  • Use situational judgment and daily operational decision-making to coordinate team activities, and support the supervisor in communicating and escalating issues and solutions.
  • Take point on daily floor maintenance execution, coordinate area activities with teammates, and maintain communication between shifts.
  • Serve as a technical resource for the team, support production operators and maintenance technicians, and collaborate with Management and Engineers to maintain compliant and efficient process equipment operations.
  • Support the expected 2-2-3 Night D shift schedule; work schedules may be modified and overtime may be requested based on business and operational needs.

Desired Qualifications

  • Associate degree or vocational/trade school certification in a relevant discipline, such as industrial maintenance, electrical, mechanical, or instrumentation.
  • Four or more years of experience in equipment maintenance within a regulated pharmaceutical or GMP manufacturing environment.
  • Experience with Overall Equipment Effectiveness (OEE), Total Productive Maintenance (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 sterile pharmaceutical manufacturing equipment, such as fill-finish lines, lyophilizers, autoclaves, isolators, and Clean-in-Place/Sterilize-in-Place (CIP/SIP) systems.
  • Maintenance planning and scheduling knowledge.
  • Prior lead technician experience in a manufacturing maintenance environment.

About the Company

Resilience

Biologics and sterile injectables CDMO

Resilience is a North American CDMO focused on biologics and sterile drug products. It provides end-to-end services from development through commercial production, including biologics development and drug substance manufacturing, aseptic fill/finish, device assembly, packaging, logistics, regulatory support, and tech transfer, all coordinated via a stage-gate process and a digital quality management system. It differentiates itself with North American-based, integrated biologics and sterile capabilities, a focus on sterile injectables and device assembly, and recent expansion into injectable pen devices for diabetes and obesity medicines. Its goal is to broaden access to complex medicines while protecting North American biopharma supply chains with dependable capacity and strong regulatory support from clinical development to commercial scale.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$3.2B
Headquarters
Blue Ash, OH
Founded
2020

Recently Posted Jobs

Explore more opportunities at Resilience

See more jobs