Facilities Engineer

Ferring Pharmaceuticals•Parsippany, NJ

8d•$90,000 - $115,000•Onsite

About The Position

As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remaining agile and true to our ‘people first’ philosophy. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world’s oldest enemy: disease. The Facilities Engineer is responsible for supporting the reliable operation, maintenance, and continuous improvement of facility and utility systems that support aseptic pharmaceutical manufacturing. This role ensures systems operate in compliance with cGMP, regulatory, and safety requirements while maintaining production continuity. The Facilities Engineer partners cross‑functionally with Engineering, Manufacturing, Quality, Validation, and Maintenance teams and serves as a technical contributor within the site facilities organization. With Ferring, you will be joining a recognized leader, identified as one of “The World’s Most Innovative Companies” by Fast Company, and honored by Fortune with inclusion on its “Change the World List,” for addressing society’s unmet needs. Ferring US is also Great Places to Work® Certified, distinguishing it as one of the best companies to work for in the country.

Requirements

Bachelor's degree in mechanical engineering, Chemical Engineering, Facilities Engineering, or related technical discipline.
3–5 years of experience in facilities engineering, utilities, or plant engineering within a pharmaceutical, biotech, or regulated manufacturing environment.
Experience supporting aseptic manufacturing or cleanroom environments preferred.
Working knowledge of facility and utility systems (e.g., HVAC, building systems, clean utilities).
Understanding of cGMP requirements, validation principles, and regulatory expectations.
Familiarity with deviation management, change control, and CAPA processes.
Experience using CMMS systems and supporting maintenance planning.
Strong problem‑solving and analytical skills.
Ability to work effectively in cross‑functional teams.
Clear written and verbal communication skills.
Organized, detail‑oriented, and able to manage multiple priorities.

Responsibilities

Support operation and maintenance of facility and utility systems supporting aseptic manufacturing (e.g., HVAC, clean utilities, building infrastructure).
Assist in monitoring system performance to ensure environmental and operational conditions meet manufacturing and regulatory requirements.
Provide technical support for routine operations, troubleshooting, and minor system improvements.
Ensure facilities and utilities are operated and maintained in compliance with cGMP, FDA, and global regulatory requirements.
Support internal and external audits and inspections; provide technical documentation and SME input as needed.
Partner with Quality and Validation to support qualification and validation activities and maintain systems in a qualified state.
Support investigations related to deviations, alarms, and system performance issues impacting manufacturing.
Participate in root cause analysis (RCA) and implementation of corrective and preventive actions (CAPAs).
Escalate complex technical issues appropriately and support resolution efforts.
Support preventive and corrective maintenance activities in collaboration with Maintenance and external service providers.
Review maintenance data and trends to help identify opportunities for reliability and performance improvements.
Support updates to SOPs, work instructions, and maintenance strategies.
Support capital and expense projects related to facility or utility upgrades, expansions, or optimization.
Participate in change control activities and review engineering documentation and drawings.
Contribute to continuous improvement initiatives focused on efficiency, reliability, and compliance.
Partner with Manufacturing, Engineering, Quality, Validation, and EHS to ensure facility systems meet production needs.
Support risk assessments, including contamination control and environmental impact evaluations.
Communicate effectively with internal stakeholders to align priorities and resolve issues.
Support oversight of vendors and contractors performing facility or utility work.
Ensure work is executed safely, compliantly, and in accordance with site procedures and expectations.