Facilities Engineer

Position Overview: We are seeking an experienced Facilities Engineer to join our team. This individual will play a pivotal role in overseeing and managing various pharmaceutical engineering projects. The ideal candidate will have a strong background in HVAC, plant utilities, or clean utilities in a pharmaceutical manufacturing environment. 

1. Facility Maintenance and Operation:
• Oversee the day-to-day operations and maintenance of the pharmaceutical manufacturing facilities, ensuring all systems are functioning optimally.
• Implement preventive maintenance programs to minimize downtime and extend the life of equipment and systems.
• Troubleshoot and address facility-related issues promptly to minimize impact on production.
2. Compliance and Safety:
• Ensure facilities comply with regulatory requirements, environmental regulations, and safety standards.
• Conduct regular inspections and audits to identify potential safety hazards or compliance issues and implement corrective actions.
• Collaborate with regulatory affairs and quality assurance teams to ensure facilities meet cGMP (current Good Manufacturing Practices) standards.
3. Energy Efficiency and Sustainability:
• Implement energy-efficient practices and sustainability initiatives to reduce the environmental impact of facility operations.
• Evaluate and recommend energy-saving technologies and practices to improve overall facility efficiency.
4. Project Management:
• Manage facility improvement projects, including renovations, expansions, and equipment installations.
• Develop project plans, budgets, and timelines, and oversee project execution from conception to completion.
• Coordinate with external contractors, engineers, and vendors to ensure projects are completed on schedule and within budget.
5. Documentation and Reporting:
• Maintain accurate records of facility maintenance activities, repairs, and upgrades.
• Prepare reports and documentation for regulatory agencies, management, and stakeholders as required.

Qualifications:

• Bachelor's degree in Mechanical Engineering, Electrical Engineering, or related field.
• In-depth knowledge of HVAC systems, hydronic utilities, steam systems, building automation systems, and/or cleanroom environments.
• Familiarity with cGMP regulations and guidelines related to pharmaceutical manufacturing facilities.
• Strong project management skills, including the ability to manage multiple projects simultaneously.
• Excellent problem-solving abilities and attention to detail.
• Effective communication skills and ability to work collaboratively in a team-oriented environment.
• Professional engineering license (PE) is a plus.