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The Site Operations, Facilities & Engineering Group provides technical support, guidance, and strategic vision to ensure that the facilities, utilities, warehouse, and laboratory equipment for BioMarin's domestic operations are designed, operated, and maintained in a manner consistent with regulatory agencies, environmental health & safety and asset lifecycle management best practices. This role will manage external vendors and contractors within a site-based Facilities & Engineering team dedicated to supporting operations across Northern California locations.
Job Responsibility:
Represent the Engineering, Facilities and Services department, collaborate, and provide advisement on non-GMP facility, utility, and equipment capital projects for Northern California campuses
Monitor and report on the status of the non-GxP campus goals and objectives
Provide Engineering support of non-GxP laboratories and their associated Facilities/Utilities systems
Act as the Facilities Engineering resource on cross-functional project teams
Collaborate, monitor, and evaluate the asset lifecycle management of non-GMP related facility systems, utility systems and equipment
Consult on the long-range planning to ensure asset replacement is scheduled and budgeted
Partner with EHS&S to support the emergency response team
Successfully plan, execute, and deliver ad-hoc requests, tasks and activities as needed
Demonstrate leadership ability including the ability to lead, motivate, develop, and directly/indirectly manage others effectively
Advance safety, health, and environmental stewardship at BioMarin through technical decisions, guidance, and leadership
Effectively manage internal and external relationships with customers, key stakeholders, and vendors
Support and drive the development of internal engineering practices and procedures
Actively participate in technical, tactical, and strategic reviews/discussions
Remain current on all training requirements
Demonstrate the ability to plan and implement small projects
Identify and champion projects and continuous improvement (CI) initiatives
Stay current with leading edge technologies, alternative energy strategies, sustainability trends and best practices
2 days on site minimum up to 4 days per week presence required with additional time necessary depending on activities
Requirements:
BS or MS in Chemical, Mechanical, or other Engineering degree from an accredited university
A minimum of 5-7 years’ experience in engineering, facilities/lab operations and clean/dirty plant utilities, preferably in the biotechnology or pharmaceutical industry
Highly proficient in deploying, managing, and improving an asset lifecycle management framework
Proficient in the relevant aspects of current Good Manufacturing Practices (cGMP), Good Clinical Practices (cGCP) and Good Laboratory Practices (cGLP)
Demonstrated successful engineering support of capital projects ranging from $1M to $10M
An understanding and awareness of latest industry standards of environmental sustainability integration to the biopharmaceutical sector
Demonstrated engineering Subject Matter Expertise (SME) in at least one of the following systems: RO/DI, Clean Dry Air (CDA), clean process gas systems, HVAC, Plant Steam, Chilled water, Condenser Water, Process Wastewater, refrigeration, or electrical systems
Strong organization, interpersonal, oral, and written communication skills
Strong analytical and problem solving abilities
Proficiency with standard office software applications, including MS Outlook, MS Word, MS Excel, MS Power Point
Proficient in utilizing Purchase Order and Spend Management Systems (e.g., Coupa, SAP, Ariba)
Proficiency in creating, editing, and reviewing, engineering/architectural drawings is required
Experience in the use of engineering software tools (e.g. CAD, Bluebeam)
Nice to have:
BMS JCI MetaSys related experience a plus
What we offer:
company-sponsored medical, dental, vision, and life insurance plans
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