Join a Leader in Pharmaceutical Manufacturing \u2014 And Build What's Next\n \nAs Spokane's Largest Manufacturing Company, Jubilant HollisterStier LLC is a well-established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support lifechanging medicines around the world. \n \nWe are nationally recognized for our expertise in producing sterile injectable vials and lyophilized products, and our Allergy business is a global leader in allergenic extracts that support treatments for allergies and asthma. Jubilant HollisterStier is proudly part of the global, Jubilant Pharma family. established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support lifechanging medicines around the world. \n \nFor the Builders, Innovators, and Doers \u2014 This Is Your Place\n \nIf you are someone who thrives on solving complex problems, improving systems, and building real solutions, you'll feel at home here. At Jubilant HollisterStier, your ideas matter \u2014 and your impact is felt globally.\n \nWhy builders choose us:\n\n Immediate impact: Your work directly supports essential medicines and allergenic therapies used worldwide.\n Benefits start on day one: Medical, Dental, Vision, FSA/HSA, Life, AD&D, and Disability benefits begin immediately because your well-being shouldn't have a waiting period. \n A career you can grow: We provide opportunities for growth, promotion, and annual raises, with midpoint compensation reserved for high performance and longevity. \n A culture of improvement: We value people who thrive on continuous improvement, innovation, and hands on contribution.\n A stable industry leader: Backed by Jubilant Pharma, we pair long term stability with forward looking innovation.\n \nIf you want to build something meaningful with a team that values your drive, skills, and ideas \u2014 you belong here.\n \nJob Description: \n \nThe Senior Manager, Equipment Maintenance is responsible for the day-to-day leadership and execution of GMP equipment maintenance, reliability, and lifecycle management activities supporting pharmaceutical manufacturing operations. This role ensures equipment uptime, regulatory compliance, and inspection readiness through effective maintenance strategies, strong people leadership, and cross-functional collaboration.\n \nThe Senior Manager translates site maintenance strategy into tactical plans and execution, leads maintenance teams and supervisors, and partners closely with Manufacturing, Quality, Validation, and Engineering to maintain a safe, compliant, and efficient operating environment.\n \nEquipment Maintenance & Reliability Execution\n\n Lead execution of preventive, predictive, and corrective maintenance programs for GMP manufacturing equipment, utilities, and critical systems.\n Ensure maintenance activities are compliant, effective, and completed on schedule.\n Monitor equipment performance, reliability metrics, and asset health; drive continuous improvement initiatives.\n Act as escalation support for complex equipment issues impacting safety, quality, or production.\n Support asset lifecycle activities, including reliability improvements and obsolescence mitigation.\n \nPeople Leadership & Supervision\n\n Lead, coach, and develop maintenance managers, supervisors, engineers, and technical staff.\n Set clear performance expectations, objectives, and development plans for direct reports.\n Foster a strong safety culture emphasizing accountability, compliance, and continuous improvement.\n Support workforce planning and day-to-day resource allocation to meet production needs.\n \nRegulatory Compliance & Inspection Readiness\n\n Ensure maintenance activities comply with cGMP, FDA, and global regulatory requirements.\n Lead or support equipment-related deviation investigations, root cause analyses, and CAPA execution.\n Maintain inspection-ready documentation including maintenance records, SOPs, and reports.\n Participate in regulatory, client, and internal audits; support audit readiness activities.\n \nCross-Functional Collaboration\n\n Partner with Manufacturing, Quality, Validation, Engineering, EHS, and Supply Chain to support operational objectives.\n Provide technical input to equipment upgrades, process improvements, and capital projects.\n Collaborate with Validation and Engineering on equipment qualification (IQ/OQ/PQ), changes, and commissioning activities.\n \nBudget & Vendor Oversight\n\n Support management of maintenance operating expenses, contracts, and service agreements.\n Oversee vendors and contractors to ensure safe, compliant, and cost-effective execution of work.\n Contribute to maintenance planning, forecasting, and continuous cost improvement efforts.\n \nQualifications: \n \nRequired Qualifications:\n\n Bachelor's degree in Engineering (Mechanical, Electrical, Industrial, Chemical, or related discipline)\n 8+ years of maintenance experience in industrial manufacturing\n 5+ years of experience in pharmaceutical or biopharmaceutical manufacturing\n 3\u20135 years of leadership experience managing maintenance teams or supervisors\n Demonstrated experience with:\n GMP equipment maintenance and reliability programs\n Deviation investigations and CAPA execution\n Inspection readiness and audit participation\n Vendor and contractor oversight\n Experience working cross-functionally in a regulated manufacturing environment\n Strong knowledge of GMP equipment maintenance, reliability engineering, and asset management\n Understanding of FDA and global regulatory requirements\n Ability to interpret technical documentation, SOPs, and engineering drawings\n Experience with maintenance management systems (CMMS)\n Proficient with data analytics, knowing what to measure and how to interpret trends.\n \nPreferred Qualifications:\n\n Certified Maintenance and Reliability Professional.\n Lean, Six Sigma, or continuous improvement training\n Project management experience\n Pharmaceutical engineering or ISPE/PDA training\n \nWorking Environment:\n\n Combination of office and manufacturing floor environment\n Occasional exposure to aseptic and controlled manufacturing areas\n Must be able to move throughout the facility as required\n \nLocation: Spokane, WA \u2014 On Site, Full- -Time\n \nShift: Mon \u2013 Fri Day Shift\n \nCompensation & Benefits That Start on Day One \u2014 Because Your Well Being Matters \n \nHiring Wage: $114,500 \u2013 $183,200 annually, with opportunities for growth, promotion, and annual raises. \n \nAt Jubilant HollisterStier, we don't believe in waiting periods. From the moment you join us, you and your family have access to a full suite of benefits designed to support your health, stability, and long-term success.\n \nStarting on your first day, you receive:\n\n Medical, Dental & Vision coverage\n Flexible Spending Accounts (FSA) & Health Savings Accounts (HSA)\n Life & AD&D Insurance\n Short-Term & Long-Term Disability Insurance\n* Employee Assistance Program\n \nUnlock Your Potential\n \nIf you're seeking a dynamic and rewarding career, we welcome your application today. Apply online: \n \nCareers - Jubilant HollisterStier \n \nJubilant HollisterStier is an EEO/AA Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. \n \nIf you require assistance applying for a position, contact:\n \nJHS-TalentAcquisition@jubl.com \n \nOur Promise: Caring, Sharing, Growing\n \nWe are committed to enhancing value for customers and stakeholders by delivering innovative and economically efficient solutions, always with care for the environment and society.\n\n