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Head of Facilities; Sr. Manager - Medical Device​/Pharma

Job in Alameda, Alameda County, California, 94501, USA
Listing for: Nano Precision Medical
Full Time position
Listed on 2026-02-06
Job specializations:
  • Management
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 155000 - 185000 USD Yearly USD 155000.00 185000.00 YEAR
Job Description & How to Apply Below
Position: Head of Facilities (Sr. Manager) - Medical Device/Pharma

Overview

We are seeking an accomplished Head of
Facilities to lead site-level operations and ensure the reliable performance, maintenance, and compliance of all facility systems. This role is critical to supporting a GMP-regulated environment and upholding the highest standards in EHS, quality, and operational excellence. The ideal candidate brings deep experience in medical device or pharmaceutical facilities management
, thrives in a fast-paced, small company, cross-functional setting, and is a proactive, solutions-oriented leader capable of navigating diverse challenges with independence and confidence.

Key Responsibilities
  • Provide strategic and hands-on leadership for all day-to-day facilities operations, serving as the primary point of contact for the site and satellite facility
  • Partner across departments to troubleshoot and resolve facilities and maintenance issues that impact operational activities
  • Lead and mentor the facilities team, ensuring successful execution of multiple projects with varying complexity, timelines, and resource needs
  • Respond to off-hours emergencies and communicate effectively with leadership during critical situations
  • Coordinate and oversee facility projects and provide technical expertise in electrical, process piping, HVAC, refrigeration, and related systems
  • Support facility construction, renovation, and expansion activities, coordinating with internal teams, architects, engineers, and contractors; assisting with project planning, scheduling, and budget tracking; and ensuring work is completed in alignment with GMP requirements, safety standards, and facility specifications
  • Support the installation, repair, commissioning, and qualification of equipment, utilities, and processes
  • Oversee calibration, preventive maintenance, and GMP equipment monitoring programs, ensuring documentation meets current regulatory and industry standards
  • Develop and optimize CMMS workflows to accurately document preventive and corrective maintenance activities
  • Oversee EHS programs, including inspections and interactions with city and regulatory agencies, ensuring compliance with hazardous materials and waste regulations
  • Manage pest control program
  • Provide oversight for building security, janitorial services, internal logistics, and onsite events
  • Conduct routine facility walkthroughs across manufacturing, quality, and technical areas to ensure compliance and readiness
  • Maintain and manage compliance documentation; lead investigations and author/review SOPs, work instructions, deviations, CAPAs, and change management records
  • Contribute to the development and review of facility policies and procedures
  • Plan and execute change controls related to qualification and facility projects
  • Manage vendor relationships, including bid solicitation, vendor evaluations, and creation of work orders and purchase orders
  • Serve as the primary facilities liaison with property management, coordinating building services, lease-related obligations, and resolution of site-level issues
  • Manages operational expenses for maintenance and services; tracks costs. Supports site OPEX; drafts CAPEX proposals; contributes to multi-year lifecycle planning
Requirements Basic Qualifications
  • Master's degree with 6+ years of facilities maintenance experience in medical device/pharma, OR
  • Bachelor's degree with 8+ years of experience in medical device /pharma facilities maintenance, OR
  • High School diploma with 12+ years of experience in medical device /pharma facilities maintenance
Preferred Qualifications
  • 10+ years of relevant experience and/or a BS/BA in a related field
  • Strong background in regulated implantable medical device or pharmaceutical environments
  • Exceptional organizational skills with the ability to plan, coordinate, and track multiple operational projects with a high level of detail
  • Demonstrated hands-on proficiency with GMP utilities and equipment, including mechanical and electrical systems, with strong troubleshooting, repair, and on-the-floor technical support capabilities
  • Experience working in cleanroom environments with knowledge of contamination-control best practices
  • Proven supervisory experience in a highly regulated manufacturing setting, with the ability to build and lead high-performing teams
  • Excellent written and verbal communication skills, along with strong interpersonal abilities
  • Demonstrated ability to manage multiple priorities and meet time-sensitive deadlines

Pay Range: $155,000 - $185,000

Benefits
  • Medical
  • Dental and Vision
  • Flexible Spending Account (FSA)
  • 401K with Company Safe Harbor Match: 100% /up to 4%
  • Life Insurance
  • Long Term Disability
  • Home Office Stipend
  • Commuter benefits
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