Support the manufacturing and process development organizations by developing and implementing preventive maintenance, on-demand maintenance, and engineering best practices.
Manage operational partnership with third party facilities support provider.
Drive implementation of site changes and facilitate day-to-day activities supporting 24/7 site operations performance to plan.
Lead, mentor, and develop high-performing teams within Facilities and Metrology by setting clear goals.
Promote a culture of ownership, technical excellence, and continuous improvement.
Oversee resource planning, talent development, and succession planning for team capability and business continuity.
Champion safety, quality, and compliance initiatives while maintaining employee engagement and morale.
Act as a key member of the site leadership team, contributing to strategic planning and overall site performance initiatives.
Manage internal staff and third-party service providers to support preventive, on-demand, and metrology maintenance.

Bachelor’s degree preferred; (Engineering, Engineering Management, or Engineering Technology).
Minimum of 7 years of experience implementing facilities and engineering best practices.
Experience in hands on implementation and support of utility/manufacturing systems within a highly regulated cleanroom manufacturing environment is required.
5 or more years related work experience with a GMP Bio-Pharma maintenance/ engineering organization, preferred.
Minimum 5 years of progressive leadership experience, including performance management and people development.
Experience in compliance Regulations that apply to Quality, Regulatory Compliance (21 CFR Part 11), Environmental Health and Safety.
Knowledge of standards related to maintenance processes, construction, equipment design and implementation into global medical device manufacturing facilities.
Experience representing Facilities in audits and Inspections both front and back room.

Associate Director, Facilities, Metrology

Key skills