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Facilities Engineer

3 months ago

Raleigh, North Carolina, United States Sequoia Biotech Consulting Full time
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.


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.

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.

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.

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.

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.

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