What are the responsibilities and job description for the Facilities Engineer position at IntePros?
Location: Northern NJ (onsite)
Job Type: Full-time
Experience Level: Mid-Level (4 years)
Job Summary
We are seeking a skilled Facilities Engineer to support manufacturing operations within the medical device industry, specifically in orthopedic implant production. This role will be responsible for maintaining and optimizing facility infrastructure, ensuring compliance with industry regulations, and leading facility improvement projects to support efficient and safe production environments.
Key Responsibilities
Job Type: Full-time
Experience Level: Mid-Level (4 years)
Job Summary
We are seeking a skilled Facilities Engineer to support manufacturing operations within the medical device industry, specifically in orthopedic implant production. This role will be responsible for maintaining and optimizing facility infrastructure, ensuring compliance with industry regulations, and leading facility improvement projects to support efficient and safe production environments.
Key Responsibilities
- Facility Maintenance & Operations: Ensure reliable operation of manufacturing facilities, cleanrooms, and support infrastructure.
- Equipment & Utility Management: Oversee HVAC, compressed air, purified water, and other critical systems to maintain optimal performance.
- Process Optimization: Identify and implement facility enhancements to improve efficiency, safety, and cost-effectiveness.
- Regulatory Compliance: Maintain compliance with FDA, ISO 13485, GMP, and OSHA regulations.
- Project Management: Lead facility expansion, renovation, and upgrade projects, coordinating with internal teams and external vendors.
- Environmental Health & Safety (EHS): Promote workplace safety and ensure adherence to environmental and occupational safety standards.
- Vendor & Contractor Coordination: Manage relationships with service providers for facility maintenance, repairs, and improvements.
- Sustainability Initiatives: Develop energy-efficient strategies to reduce facility costs and environmental impact.
- Education: Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Facilities Management, or a related field.
- Experience: Minimum 4 years of facilities engineering experience in a medical device or regulated manufacturing environment, preferably with exposure to orthopedic implant production.
- Technical Skills:
- Strong understanding of GMP, FDA, and ISO 13485 regulations.
- Experience with HVAC, cleanroom operations, and utility management.
- Proficiency in AutoCAD, CMMS, and facility management software is a plus.
- Knowledge of EHS and OSHA compliance requirements.
- Soft Skills:
- Excellent problem-solving and troubleshooting abilities.
- Strong communication and project management skills.
- Ability to work cross-functionally with engineering, manufacturing, and regulatory teams.
- Work with cutting-edge medical device technology that improves patient outcomes.
- Be part of a dynamic and collaborative engineering team.
- Competitive salary, benefits, and career growth opportunities.
