Maintenance Technician IV - IDAP (Night Shift)

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 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. Job 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. Documentation & Compliance 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. Training & Development 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). Education & Experience Minimum Qualifications 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., 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. Preferred Qualifications 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). Physical & Work Environment This role is primarily a non-Sedentary role. This can include climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects. Visual acuity such as working with data & figures, viewing computer terminal, extensive reading, operating machinery, operating motor vehicles, general observations of facilities, etc. Participation in an occupational health program, which can include medical assessment, surveillance, vaccination, and testing. Use of personal protective equipment, which can include respirators, Personal Air Purifying Respirators [PAPR], gowns, gloves, face protection, other barrier equipment, etc. All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role. The items described here are representative of those that must be met successfully to perform the essential functions of this job. Work Schedule 12-hour nightshift – 2/2/3 6:00pm-6:30am Sponsorship or support for work authorization, including visas, is not available for this position. Equal Employment Opportunity Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Benefits annual cash bonus program 401(k) plan with a generous company match our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision) family building benefits life and disability insurance paid vacation paid holidays other paid leaves of absence tuition reimbursement and support for caregiving needs Our target base pay hiring range for this position is $28.50 - $46.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Company Culture RESILIENCE is a first-of-its-kind manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disruption. Founded in 2020, the company is building a sustainable network of high-tech, end-to-end manufacturing solutions to ensure the medicines of today and tomorrow can be made quickly, safely, and at scale. RESILIENCE will offer the highest quality and regulatory capabilities, and flexible and adaptive facilities to serve partners of all sizes. By continuously advancing the science of biopharmaceutical manufacturing and development, RESILIENCE frees partners to focus on the discoveries that improve patients’ lives. #J-18808-Ljbffr Resilience