Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. JOB SUMMARY The Maintenance Technician II-III is responsible for executing, maintaining and improving the cGMP equipment PM Program at AGC Biologics facilities in Bothell, WA. This is a key position that ensures the reliability of equipment for new Bio-Manufacturing Facility as well as maintaining the current operation of the existing facilities. ESSENTIAL JOB DUTIES/RESPONSIBILITIES Perform preventative maintenance work on complex manufacturing equipment such as bioreactors, processing pumps, valves, RO/DI water systems, distillation systems, distribution systems, steam generation, compressed air systems and other manufacturing and utility system equipment. Perform troubleshooting, installations and repairs of complex instrumentation on production, laboratory and facility systems, ensuring all systems and devices are calibrated in accordance with manufacturer's specifications and AGC Biologics internal SOP's. Maintain a safe work environment; work in a safe manner following all safety SOP's and wear Personal Protective Equipment as required. Maintain assigned area of ownership within the facility to support inspection readiness and general facility upkeep for support of clinical and commercial manufacturing. Complete maintenance work orders within the allotted time. Maintain all assigned maintenance records, work orders, and investigations in an orderly and accurate manner in compliance with cGMP's by the utilization of the site CMMS and Document Management Systems. Assist Equipment Owners determine the appropriate maintenance information for their processes through the evaluation of equipment specifications. Assist in qualification activities related to Instrumentation and Process improvement projects. Assist with Vendors to get maintenance quotes, etc., and Interface with maintenance contractors, ensuring work is compliant with AGC SOP's and cGMP's within the facility. Assist in the review and development of Maintenance Department Procedures. Ensure compliance with all applicable regulatory agencies including FDA, OSHA, CFR, etc. LEADERSHIP SKILLS Strong written, verbal and interpersonal communications skills. Strong analytical and problem solving skills and experience applying these skills to resolve technical problems. Demonstrated good interpersonal skills, customer focus, and professionalism. Ability to work quickly and effectively without constant supervision. Ability to work in a fast-paced environment. QUALIFICATIONS Required: High School Diploma with a minimum of 6 years in overall maintenance activities of which at least 3 years must be in a cGMP or other FDA regulated operation or a bio-tech facility is required. Experience with Start-Up & Commissioning of cGMP Facility. Strong knowledge of maintenance procedures and techniques related to manufacturing and utility systems, that may include Autoclaves, CIP/SIP systems, Incubators, Analytical equipment, and Process tanks as well as other facility equipment. Strong skills and experience in MS Office products (Word, Excel, Outlook, PowerPoint). Demonstrated ability to works on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations to management Knowledgeable of Electrical, Mechanical, Control/SCADA, PLCs, Process Improvement Methodologies, Root Cause Analysis (RCA), Biotechnology, Pharmaceutical, Medical Device Utilities Process. Knowledge of documentation requirements for cGMP manufacturing. Ability to read, interpret, and troubleshoot engineering drawings, P&IDs, and electrical schematics with assistance when needed. Preferred: Computer literate in a CMMS (Computerized Maintenance Management Software) such as Blue Mountain or similar computer-based maintenance program desirable. Physical Requirements (US Only): Ability to work in prolonged sitting, standing, walking, bending, stooping and stretching. Ability to climb ladders and stairs of various heights. Ability to be exposed to wet or humid conditions. Ability to be exposed to outdoor weather conditions. Ability to be exposed to noisy environments. Ability to regularly lift and/or move up to 45 pounds and occasionally lift and/or move up to 70 pounds briefly. COMPENSATION RANGE $28.73 - $44.26 per hour depending on experience Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook! AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com.