(CW) Laboratory Move Project Manager (CONTRACT/TEMPORARY)

BioMarin Pharmaceutical•Novato, CA

7d•Hybrid

About The Position

BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions. Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world. BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. This will be hybrid in Novato 2 days a week during move planning and 5 days a week during the actual move. Working 8 am to 5 pm

Requirements

Bachelor’s degree in Engineering, Life Sciences, Facilities Management, or a related field required
Minimum of 8–10 years of experience in project management, laboratory operations, or facilities-related roles
Demonstrated hands-on experience managing complex laboratory relocations, including large-scale moves (e.g., 300+ pieces of equipment)
Proven experience working within biologics or regulated laboratory environments preferred
Experience coordinating with equipment vendors, OEMs, and cross-functional stakeholders
Proficiency in project management tools and methodologies (e.g., MS Project, Smartsheet)
Strong understanding of laboratory equipment lifecycle (shutdown, transport, calibration, commissioning and qualification as necessary)
Familiarity with facility systems including electrical, HVAC, plumbing, process gases, process waste, and laboratory ventilation systems
Strong project and program management skills
Cross-functional leadership and stakeholder management
Risk assessment and mitigation capability
Technical expertise in laboratory operations and equipment
Excellent communication, organization, and problem-solving skills
May require periodic on-site presence during move execution phases
Ability to manage high-pressure timelines and complex logistical coordination

Nice To Haves

Project Management certification preferred

Responsibilities

Define project scope, timeline, milestones, and critical path for laboratory relocation
Develop and manage relocation budgets, including vendor costs, calibration services, and waste disposal
Assess readiness of the new facility, ensuring alignment with technical requirements (electrical, data monitoring, HVAC, plumbing, ventilation)
Attend project OAC and specification development meetings
Serve as the primary liaison across stakeholders including laboratory teams, project management teams, equipment owners, EHS&S, Facilities, Real Estate, and Information Management
Lead regular project meetings and status updates to ensure alignment and issue resolution
Establish contingency and risk mitigation plans for equipment damage, delays, or operational impacts
Assign and coordinate internal team responsibilities, including labeling, inventory tracking, and data management
Ensure adherence to safety protocols for decommissioning, decontamination, and clearance of laboratory equipment and spaces
Secure and maintain required regulatory permits and approvals (e.g., DEA, EPA, DOT, FDA, CDC)
Ensure compliance with company policies, regulatory requirements, and industry standards
Maintain a comprehensive inventory of all assets, including equipment, chemicals, biological materials, consumables and spare parts (CMMS), and office supplies.
Direct and supervise on-site moving activities, including sequencing, logistics coordination, and safety enforcement
Coordinate with specialized vendors for packing, transportation, and handling of sensitive equipment
Coordinate equipment recalibration, testing, and qualification with OEMs and vendors
Verify proper installation, utility connections, and placement of all laboratory equipment
Conduct final inspections and walkthroughs with safety and facilities teams to certify readiness of the new laboratory
Support formal closure of the previous space and operational release of the new environment
Support the organisation’s commitment to environmental protection, injury prevention, and continual improvement of EHS management systems.
Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.