HVAC Engineer, Facilities

Minimum of 10 years’ experience with HVAC and related equipment within the Biotechnology industry.

Knowledge of FDA and EU clean room classifications and operations, specifically ISO7 and Grade C clean room environments.

Experience in GxP manufacturing, utility and facility equipment design, implementation, maintenance and reliability.

Leadership roles in support of projects and sustaining operations on HVAC equipment.

Experience with a Computerized Maintenance Management System (CMMS).

Experience with Building Automation Systems (BAS) or Building Management Systems (BMS).

The Engineer Staff I, Facilities will be responsible for the design, operation and maintenance of GMP and non-GMP Heating Ventilation and Air Conditioning (HVAC) equipment and systems in support of formulation, development and commercialization of innovative therapies at a GMP biopharmaceutical manufacturing plant.

This is an individual contributor role within the Facilities Engineering team, working collaboratively with Maintenance, Calibration, I&C, and Quality functions.

Oversee the design, specification and selection of HVAC and Air Handling Units (AHU) for GMP manufacturing clean rooms, Quality Control (QC) labs, warehouses, as well as for general facilities, non-GMP, office and amenities.

Oversee the design, specification and selection of humidity control equipment for GMP manufacturing clean rooms, labs, and warehouses.

Responsible for reliability and maintenance of HVAC, AHU and Humidity control equipment.

Improve and develop preventative maintenance plans, standard operating procedures (SOP’s) and corrective maintenance practices and procedures.