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Sr Manager Equipment Maintenance

Job in Spokane, Spokane County, Washington, 99201, USA
Listing for: Jubilant Bhartia Group
Full Time position
Listed on 2026-06-01
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering, Manufacturing Operations / Plant Manager, Manufacturing Engineer
Job Description & How to Apply Below
Join a Leader in Pharmaceutical Manufacturing - And Build What's Next

As Spokane's Largest Manufacturing Company, Jubilant Hollister Stier LLC is a well-established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support life changing medicines around the world.

We 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 Hollister Stier 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 life changing medicines around the world.

For the Builders, Innovators, and Doers - This Is Your Place

If you are someone who thrives on solving complex problems, improving systems, and building real solutions, you'll feel at home here. At Jubilant Hollister Stier, your ideas matter - and your impact is felt globally.

Why builders choose us:

* Immediate impact:
Your work directly supports essential medicines and allergenic therapies used worldwide.

* 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.

* A career you can grow:
We provide opportunities for growth, promotion, and annual raises, with midpoint compensation reserved for high performance and longevity.

* A culture of improvement:
We value people who thrive on continuous improvement, innovation, and hands on contribution.

* A stable industry leader:
Backed by Jubilant Pharma, we pair long term stability with forward looking innovation.

If you want to build something meaningful with a team that values your drive, skills, and ideas - you belong here.

Job Description:

The 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.

The 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.

Equipment Maintenance & Reliability Execution

* Lead execution of preventive, predictive, and corrective maintenance programs for GMP manufacturing equipment, utilities, and critical systems.

* Ensure maintenance activities are compliant, effective, and completed on schedule.

* Monitor equipment performance, reliability metrics, and asset health; drive continuous improvement initiatives.

* Act as escalation support for complex equipment issues impacting safety, quality, or production.

* Support asset lifecycle activities, including reliability improvements and obsolescence mitigation.

People Leadership & Supervision

* Lead, coach, and develop maintenance managers, supervisors, engineers, and technical staff.

* Set clear performance expectations, objectives, and development plans for direct reports.

* Foster a strong safety culture emphasizing accountability, compliance, and continuous improvement.

* Support workforce planning and day-to-day resource allocation to meet production needs.

Regulatory Compliance & Inspection Readiness

* Ensure maintenance activities comply with cGMP, FDA, and global regulatory requirements.

* Lead or support equipment-related deviation investigations, root cause analyses, and CAPA execution.

* Maintain inspection-ready documentation including maintenance records, SOPs, and reports.

* Participate in regulatory, client, and internal audits; support audit readiness activities.

Cross-Functional Collaboration

* Partner with Manufacturing, Quality, Validation, Engineering, EHS, and Supply Chain to support…
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