he Facilities and Maintenance Manager is responsible for ensuring the efficient, safe, and compliant operation of all infrastructure, critical systems, and production support equipment in a regulated medical device manufacturing environment. This role leads preventive and corrective maintenance strategies, manages infrastructure improvements, and ensures compliance with quality standards and environmental, health, and safety (EHS) requirements.
Responsible for adhering to EHS, quality, and TEOA product standards within the framework of customer specifications and TE’s internal procedures
RESPONSIBILITIES & TASKS
Lead and supervise the facilities and maintenance team, including engineers, technicians, and external vendors.
Develop and manage preventive and predictive maintenance programs for equipment and infrastructure.
Ensure compliance with medical sector regulations (e.g., ISO 13485, FDA) and EHS norms and policies.
Manage maintenance budgets, service contracts, and vendor relationships.
Oversee critical site systems (HVAC, compressed air, water treatment, electricity, etc.).
Lead or support engineering projects such as equipment installation, expansions, or renovations.
Ensure proper calibration and validation of equipment in accordance with quality system requirements.
Support audits and inspections (internal, regulatory, or customer) with appropriate documentation and processes.
Promote a culture of safety, sustainability, and continuous improvement.
Identify and implement innovative solutions in maintenance, energy efficiency, and facility management that drive continuous improvement and sustainability.
Serve as a trusted position, handling sensitive site information, budget decisions, and key relationships with strategic vendors.
Supervise and coordinate outsourced site services, including cleaning, landscaping, security, and other general services, ensuring compliance with quality, safety standards, and applicable regulations
COMPETENCIES & SKILLS
Over 5 years of experience in facilities and maintenance management, preferably in a regulated industry (medical devices, pharmaceuticals, biotechnology).
Knowledge of regulatory standards (ISO 13485, FDA, GMP).
Leadership skills, effective communication, and ability to manage multidisciplinary teams.
Experience in budget management, project planning, and process improvement.
Ability to work in a highly regulated, quality-focused environment.
Advanced English (desirable for multinational companies).
Knowledge of Lean, Six Sigma, or TPM methodologies
JOB REQUIREMENTS
Education:
Bachelor’s degree in Industrial Maintenance Engineering, Mechanical, Electronics, Electromechanics, or related fields. MBA or postgraduate studies desirable.
Experience:
Minimum of 5 years of experience in medical device manufacturing, with at least 3 years in a leadership role.