Green Engineering Jobs (NOW HIRING)

JOBTITLE:FacilitiesEngineering Manager

LOCATION:50Northern Ave., Boston, Massachusetts 02210

OPENINGS:1

DUTIES:

• Lead engineering efforts across clean utilities, equipment, and infrastructure for multiple sites and functions, spanning all project phases including conceptual design, detailed design, construction, startup, commissioning, validation, and ongoing operations.

• Facilitate and perform design and technical reviews for complex, regulated capital projects with emphasis on efficiency, compliance, sustainability, and cost-effectiveness.

• Drive multi-site engineering standardization by authoring specifications, design guidelines, and policies that serve as benchmarks for capital projects and operations.

• Manage cross-functional teams including in-house staff, scientific partners, and seasonal consultants to execute critical commissioning and validation projects.

• Perform specialized engineering assessments for advanced manufacturing, QC, and R&D capital equipment with uniqueexpertisein cell and gene therapy (CGT), oral solid dosage (OSD), and medical devices.

• Ensure alignment with FDA, NFPA, OSHA, EMA, and MHRA requirements, serving as a subject matter expert who interprets evolving regulations and proactively embeds compliance strategies into facility and equipment design.

• Lead hazard analyses, risk assessments, and safety reviews for pharmaceutical facilities and equipment, applying risk management principles to protect patient safety, ensure product quality, and safeguard operations.

• Champion sustainability initiatives, driving energy reduction, carbon emissions reduction, and green engineering improvements across facilities and equipment.

• Integrate digital engineering tools (BIM, Revit) to modernize facility design,optimizeperformance, and support predictive maintenance.

• Bridge science, engineering, and business strategy, ensuring facilities and equipment are future-ready and adaptable to evolving scientific and technological advancements.

• Standardizeand transfer engineering best practices across multiple sites, improving efficiency, cost savings, and consistency across diverse modalities.

• Coordinate critical project documentation, including Engineering Turnover Packages (ETOP), BIM/Revit deliverables, and integration into facility management systems, ensuring long-term operational readiness.

• Support leadership in shaping the strategic value proposition of Engineering, advancinginnovationand ensuring capital investments align with long-term business and scientific growthobjectives.

REQUIREMENTS:Employer will accept aBachelor'sdegree, or foreign equivalent, in Engineeringor a related field and4years of experience in the job offered or ina Facilities Engineering Manager-related occupation.

Position requires demonstrable experience in the following:

• Proficient in AutoCAD, Revit, BIM (Building Information Modeling) for facility design, documentation, and integration into facility management systems.
• Expertisein URS, FAT, SAT, IQ, OQ, and PQ protocols; skilled in commissioning scripts, validation protocols, and turnover packages (ETOP) for GMP-regulated facilities.
• Advanced application of PHA, HAZOP, and Risk Assessment principles toidentify, evaluate, and mitigate risks in pharmaceutical operations.
• Deep knowledge of FDA, EMA, MHRA, OSHA, NFPA, and ISPE Baseline Guides, with the ability to interpret evolving regulations and embed compliance strategies into design and operations.
• Specializedexpertisein WFI (Water for Injection), Clean Steam, HVAC, Compressed Air, Process Gases, and Purified Water Systems; experienced in capacity modeling, troubleshooting, and system impact assessments.
• Hands-on experience with CGT (aseptic processing, isolators), OSD (unit operations and continuous processing lines), and medical device assembly and packaging equipment.
• Support program readiness for commercial launch for all modalities (CGT, OSD, and Medical Device) by managing capital projects efficiently, within budget and schedule.
• Skilled in equipment specifications for equipment used in OSD and CGT manufacturing sites and integration with facility infrastructure including HVAC, process systems, utilities,qualificationand operation in GMP environment.
• Skilledin MS Project as well asThinkCelland Smartsheet for scheduling, project execution, and resource management.
• Expertisein authoring technical standards for multiple sites for equipment (Air Handling Systems, Chillers, and Boilers) and facilities (Clean Rooms, Clean utility Systems, and Clean Process gas Systems).
• Strong ability to coordinate engineering, R&D, quality, operations, EH&S, and consultants.
• Ability to review and approve submittals and RFIs fromprojectteam.
• Proficientin Veeva Document Management, Coupa Procurement Management, Procore Construction Management, and Nuvolo Asset Management.
• Proficient inEnteliWebBuilding Management System, Metasys Building Management System, andViewlinc/VeriteqEnvironmental Monitoring System.
• Knowledge of CFR Part 11 Compliance and automation requirements for manufacturing and lab equipment.

Rate ofPay:$154274.00- $177600.00

CONTACT:Send Resume tofuturetalent@vrtx.com.Reference12140.835. EOE.