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Catalent, Inc. is a leading global CDMO. We are seeking a Senior Facilities Engineer to coordinate preventative and routine maintenance across all facility spaces at our San Diego site, ensuring safety, compliance, and operability.
You will partner with internal teams and vendors, supporting GMP operations and site-wide critical systems. The role offers growth in a fast-paced GMP environment, with opportunities to lead validation, calibration, change control, and facilities projects while
Work Schedule: Monday-Friday, 8:00am-4:30pm 100% on-site (San Diego)
Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Our purpose-built San Diego location provides comprehensive clinical supply services including clinical supply management, primary and secondary packaging, complex labeling services, clinical storage, distribution, and clinical returns and destruction, and will also include stability chambers. Located less than a mile from Catalent’s West Coast early-phase oral drug product development center of excellence, customers choosing this convenient Catalent location can now enjoy a fully integrated development, clinical supply manufacturing and distribution solution.
The Senior Facilities Engineer is responsible for coordinating and executing preventative and routine maintenance across all facility spaces—including manufacturing suites, production rooms, labs, warehouse areas, offices, and shared spaces—while serving as the primary point of contact for all internal and external maintenance needs. Partnering with both internal teams and vendors, this role ensures the building remains safe, compliant, and fully operational.
Under direction from the Technical Services Manager, the Senior Facilities Engineer acts as a technical expert across multiple engineering disciplines, supporting daily GMP operations. This position offers the opportunity to drive site-wide impact, take ownership of critical facility systems, and play a key role in a growing, fast-paced GMP environment with strong visibility and long‑term career growth.
Maintain GMP‑compliant building areas, manufacturing suites, and support spaces, ensuring all systems and equipment remain within specification.
Oversee general facility maintenance and repairs, including mechanical, electrical, plumbing, painting, and overall building infrastructure.
Manage GMP clean compressed air, nitrogen, RO/DI water systems, and site HVAC through the Building Management System (BMS).
Oversee the work order system, asset management, and facility documentation within JDE.
Manage all refrigerators, freezers, and temperature‑controlled environments to ensure proper monitoring and performance.
Coordinate and oversee external vendors performing repairs, preventative maintenance, and GMP‑related work.
Maintain facility fire suppression, fire safety equipment, and support EH&S with fire extinguisher and eye wash compliance.
Support overall site safety, security, and emergency response initiatives, including participation on the safety committee.
Lead or support validation, calibration, change control, facilities projects, tenant improvements, and off‑site construction activities.
Manage exterior site maintenance (parking areas, roof, lighting, landscaping, generator) and assist with corporate event setup as needed.
All other duties as assigned.
High school diploma or GED required.
Bachelor’s degree in Engineering or equivalent technical apprenticeship/certifications preferred.
Minimum of 10 years of relevant facilities experience with strong experience in HVAC systems and solid working knowledge of plumbing, electrical, lighting, and general building trades/construction methods.
Minimum of 3 years of experience in a cGMP environment or related pharmaceutical/biotechnology setting preferred.
Demonstrated ability to lead or support validation, calibration, change control, and facilities‑related projects, applying sound technical judgment and ensuring activities align with GMP standards.
Strong written and verbal communication skills with a customer‑focused mindset; able to work independently or collaboratively across cross‑functional teams in fast‑paced or time‑sensitive situations.
Highly organized and proactive with strong problem‑solving abilities; able to prioritize and manage multiple tasks while maintaining attention to detail.
Comfortable with technology and capable of quickly learning new systems and software; basic proficiency with common workplace tools (e.g., MS Office) preferred.
Able to frequently stand, walk, sit, kneel, reach, and push/pull, with the ability to lift up to 45 lbs.; must maintain 20/30 corrected vision and be able to work occasionally in cold, humidity‑prone, wet, or temperature‑variable environments, including temperature‑controlled refrigerators and freezers.
The anticipated salary range for this role in California is $100,000 - $110,000.
The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc.
including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
can find our California Job Applicant Notice HERE.
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life‑enhancing and life‑saving treatments for patients annually.