Jobs at BioMarin Pharmaceutical Inc. (Now Hiring) — 113 open — Page 3

Who We Are

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.

About Technical Operations

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.

CONTRACT ROLE 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***

Job Title: Laboratory Move Project Manager

Job Summary / Purpose
The Laboratory Move Project Manager is responsible for planning, coordinating, and executing complex laboratory relocations involving high-value scientific equipment, sensitive materials, and regulated environments. Interface with MEPT trades to ensure successful lab integration into a new facility while maintaining continuity in the current labs. This role ensures seamless transition of laboratory operations with minimal disruption to research activities while maintaining compliance with safety, regulatory, and quality standards.
Required Qualifications

Education
• Bachelor’s degree in Engineering, Life Sciences, Facilities Management, or a related field required
• Project Management certification preferred
Experience
• 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

Technical Skills
• 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

Roles and Responsibilities
1. Pre-Move Planning & Strategy
• 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

2. Coordination & Communication
• 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
3. Compliance & Risk 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


4. Logistics & Execution
• 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

5. Post-Move Activities
• 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

Key Competencies
• 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

Additional Information
• May require periodic on-site presence during move execution phases
Ability to manage high-pressure timelines and complex logistical coordination

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.

Equal Opportunity Employer/Veterans/Disabled

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Ireland Safety Responsibility 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.
Ireland Safety Responsibility
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.