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Job opportunity
Engineer - Facilities and HVAC Systems
BioPharma Consulting JAD Group
Juncos, Juncos, PR
Source: BioPharma Consulting JAD Group careers · View original posting
- Employment
- contract
Employer job description
From BioPharma Consulting JAD Group's posting. “We” and “our” refer to the employer.
We are seeking an Engineer to provide engineering support for the operation, troubleshooting, optimization and modification of HVAC, utilities and facility systems at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. The Engineer applies engineering principles to resolve operational issues, support preventive maintenance strategies, and execute facility modifications and capital projects, working closely with Facilities, Maintenance, Manufacturing, Quality, Validation, EHS and external engineering and service providers.
Key Responsibilities
- Provide engineering support and troubleshooting for HVAC, utilities and facility systems to ensure safe, reliable, efficient and GMP-compliant operation.
- Act as technical expert for equipment and systems; become actively involved in daily operations to meet schedules or resolve complex problems.
- Audit the operational performance and regulatory compliance of equipment and systems.
- Support preventive maintenance strategies and develop requirements and recommendations for system modifications.
- Support design, engineering and construction of facility modifications and capital projects within schedule and budget, working with consultants, architects and engineering firms.
- Obtain and critique quotes for equipment modifications or installations; prepare basic cost estimates and schedules.
- Organize, analyze and present results for operational issues and engineering projects.
Requirements
- Education
- Master's degree; OR Bachelor's degree in Engineering + 2 years of engineering experience
- Availability for weekend support and 12-hour shifts during the implementation phase
Preferred Qualifications
- Experience with HVAC, utilities and/or facility systems in a regulated pharmaceutical/biotech environment
- Working knowledge of pharmaceutical/biotech processes and GMP/GLP
- Familiarity with validation processes and validation protocol writing/execution
- Experience with facility modifications, preventive maintenance and capital projects
- Documentation in a highly regulated environment
- Key Skills
- Problem solving and applied engineering; analytical troubleshooting
- Technical report writing and presentations
- Personal organization and managing change
- Bilingual English/Spanish communication
Benefits
- Contract position: approximately 5.5 months (November 2026 – April 2027), with possible extension
- Shift: Non-standard shift – 12-hour shifts (approximately 48 hours/week), including weekend support during the implementation phase
- On-site in Juncos, Puerto Rico
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