Engineering Planner, Senior
Bothell, WA - USA
Job Summary
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 Planner is responsible for planning scheduling and coordinating site maintenance and calibration activities. The role ensures reliable scheduling and supports Preventive Maintenance and Calibration compliance while partnering with Maintenance Reliability and Production teams to support asset reliability and efficient operations.
About Our Engineering Team
You will be part of a collaborative Maintenance and Engineering team that supports safe compliant and reliable operations. The team works closely with Reliability Production Quality and external partners to deliver planned maintenance and calibration activities in a fastpaced manufacturing environment. Strong teamwork operational discipline and a safetyfirst mindset are core to how the team operates.
Key Responsibilities
Develop manage and maintain site maintenance and calibration schedules.
Plan and coordinate all planned maintenance and calibration activities using CMMS.
Monitor track analyze and report schedule performance; implement adjustments as needed to maintain PM and Calibration compliance.
Identify and implement improvements to maintenance planning and execution processes.
Partner with maintenance teams VMI suppliers and vendors to ensure materials are available while minimizing inventory value.
Oversee parts inventory accuracy cycle counts and physical inventories; provide required reporting.
Perform initial screening of incoming work orders define scope and determine the appropriate level of planning.
Conduct field walkdowns to identify job requirements safety hazards materials tools calibration standards and equipment access needs.
Develop job plans labor and material estimates and material lists to maximize efficiency and wrench time.
Research and gather engineering specifications drawings and technical documentation as required.
Capture and analyze maintenance data including losses costs breakdowns and tag resolution.
Support TPM and RCMbased maintenance initiatives.
Coordinate directly with contractor resources to ensure work order scope and expectations are clearly understood.
Support Quality Systems activities as needed including investigations and reporting.
Serve as backup to CMMS Administrators.
Participate in budget preparation cost tracking and cost trend analysis; recommend opportunities for continual improvement.
Qualifications & Experience
Required:
Associates degree or equivalent technical experience.
Minimum of 8 years of maintenance planning and scheduling experience.
Experience with Computerized Maintenance Management Systems (CMMS).
Experience developing and maintaining maintenance documentation reports investigations and SOPs.
Experience planning and scheduling shutdowns (major and minor).
Working knowledge of planning and scheduling methods including Gantt charts Critical Path Analysis and resource leveling.
Proficiency with Windowsbased applications.
Strong attention to detail with a consistent ability to deliver accurate errorfree work.
Flexibility to adapt to changing priorities schedules and business needs.
Preferred:
FDA / cGMP experience in a regulated manufacturing environment.
Experience with CMMS platforms such as Maximo BMRAM or similar systems.
Formalities
Location: Onsite Bothell Washington
Schedule: Full-time onsite
Compensation Range: $83920 - $115390
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