Maintenance Technician I
Maintenance Technician I
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Job Description
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
We are seeking a Maintenance Technician I to join our team at our Bothell WA site. This role is responsible for executing maintaining and improving the cGMP equipment preventative maintenance (PM) program to ensure the reliability of all manufacturing and utility systems. The ideal candidate brings hands-on mechanical aptitude a sense of ownership and thrives in a dynamic GMP-regulated environment.
Location: Bothell WA
Schedule: Monday Friday day shift 7:00 AM 4:00 PM
Compensation: $25.65 $35.27 per hour
Essential Job Duties / Responsibilities
Perform basic preventative maintenance on complex systems including bioreactors RO/DI water systems processing pumps valves distillation units steam generation and compressed air systems.
Assist in troubleshooting installation and repair of instrumentation on production lab and facility systems; ensure calibration to specifications.
Maintain a safe work environment in accordance with safety SOPs and PPE requirements.
Own assigned facility areas to ensure inspection readiness and overall upkeep in support of clinical and commercial manufacturing.
Complete assigned maintenance work orders within specified timelines.
Accurately document maintenance records work orders and investigations using the site CMMS and Document Management Systems in compliance with cGMP.
Support equipment owners in evaluating specifications to determine maintenance requirements.
Participate in qualification and process improvement activities related to equipment and instrumentation.
Escort and support vendors performing maintenance work ensuring compliance with SOPs and regulatory standards.
Contribute to the development and review of maintenance department procedures.
Ensure adherence to regulatory requirements including FDA OSHA and CFR.
Leadership Skills
Strong written and verbal communication skills.
Demonstrated professionalism customer focus and teamwork.
Ability to work independently and manage multiple priorities.
Comfortable operating in a fast-paced GMP-regulated environment.
Qualifications
Required:
High school diploma or equivalent.
Minimum 2 years of experience in industrial maintenance or completion of a related technical training/apprenticeship program.
Ability to learn and apply maintenance techniques for GMP systems (e.g. CIP/SIP systems autoclaves incubators).
Developing analytical and problem-solving skills.
Proficiency in Microsoft Office (Word Excel Outlook PowerPoint).
Willingness to learn cGMP documentation practices.
Preferred:
Experience with CMMS platforms such as Blue Mountain or similar.
Physical Requirements
Ability to sit stand walk bend stoop and stretch for extended periods.
Ability to climb stairs and ladders of various heights.
Tolerance for wet humid outdoor or noisy environments.
Ability to regularly lift/move up to 45 lbs and occasionally up to 70 lbs.
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 2500 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.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.
Required Experience:
IC
Employment Type
Full-Time
