Facilities Engineer

Aspect Biosystems

Colorado

On-site

USD 94,000 - 102,000

Full time

14 days+

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Benefits offered by this job

Equity
Comprehensive benefits package
Support for continuous learning and career progression

Job summary

Aspect Biosystems is seeking an experienced Engineer in Colorado to provide technical support for the Fremont site’s metrology program. You will handle calibration of manufacturing equipment and utilities, draft documentation, and support quality compliance during equipment installation. Candidates should have a Bachelor's/Master's in Engineering and 3-5 years of experience in a regulated industry. The annual salary range for this position is $94,000 - $102,000, along with additional benefits and equity opportunities.

Qualifications

  • 3-5 years of experience in a regulated industry (Biotech, Pharma, Med Device), preferably in metrology or facility engineering.
  • Familiarity with reading and interpreting P&IDs, drawings, specifications, and reviewing vendor documentation.
  • Experience with coordinating multiple vendor schedules simultaneously.

Responsibilities

  • Executing the site-wide metrology program and ensuring compliance.
  • Supporting CQV of manufacturing equipment and utilities.
  • Drafting and maintaining lifecycle documentation.
  • Monitoring facility operations and supporting HVAC system maintenance.
  • Facilitating vendor management and ensuring compliance with safety and quality standards.

Skills

Knowledge of NIST standards
HVAC
Utility Systems (including WFI, gases)
Coordination of vendor schedules
Reading and interpreting P&IDs
Conducting FAT and SAT testing
Problem-solving
Attention to detail

Education

Bachelor's or Master's in Engineering

Job description

We are looking for an enthusiastic, experienced Engineer to join our team in Fremont. Reporting to the Senior Engineer, you will provide essential technical support for the Fremont site’s metrology program and facility operations. This role is a mix of hands‑on technical execution and project coordination, ensuring that manufacturing equipment and site utilities (HVAC, electrical, and mechanical) are calibrated, maintained, and compliant with site standards. You will be directly contributing to our groundbreaking programs and our mission to develop bioprinted tissue therapeutics to transform the lives of people with serious diseases.

Responsibilities
  • Executing the site‑wide metrology program, coordinating the calibration and maintenance of all instrumentation to ensure systems remain within established tolerances and support a validated state of operation.
  • Supporting the Commissioning, Qualification, and Validation (CQV) of manufacturing equipment and facility utilities (HVAC, water, and gas systems) under the guidance of the Senior Engineer, applying risk‑based strategies and GAMP5 standards.
  • Drafting and maintaining lifecycle documentation, including URS, FMEAs, and IQ/OQ/PQ protocols. Assisting in the standardization of equipment intake processes and periodic reviews to increase site efficiency.
  • Coordinating with the Manufacturing team during the installation and modification of new systems, acting as a technical resource for equipment design reviews and technology transfers.
  • Monitoring facility operations and utilities as well as supporting the maintenance of HVAC and mechanical systems to ensure cleanroom environments and production areas meet performance specifications.
  • Managing and handling facility gas systems, including under GMP requirements (daily checks, inventory control of gas cylinders/spares, physically changing/replacing cylinders, etc).
  • Assisting in regulatory inspection readiness by organizing engineering and validation packages (FDA, EMA, etc.) and acting as a secondary Subject Matter Expert (SME).
  • Administering the Maintenance Management System (CMMS), BMS, FMS, performing data entry and tracking for the asset registry, PM schedules, and replacement parts inventory. Assisting in root‑cause investigations for equipment failures or out‑of‑tolerance events will be among your duties.
  • Facilitating vendor management and test scheduling, ensuring third‑party contractors complete calibrations, repairs, preventive maintenance, equipment install, and external IQ/OQ testing on time and in compliance with site safety, quality, and Good Documentation Practice (GDP) standards.
  • Overseeing the security of site, facility maintenance and cleaning of controlled and non‑controlled areas.
  • Creating and maintaining accurate documentation, SOPs, and records for calibrations, maintenance, facility, and utilities.
  • Other duties as required.
Qualifications & Experience
  • Experience & Education: A bachelors or masters in engineer and 3–5 years of experience in a regulated industry (Biotech, Pharma, or Med Device), with a strong preference for experience in metrology or facility engineering. We will consider applicants with a mix of industry and educational background.
  • Skills: Knowledge of NIST standards, HVAC, Utility Systems (including WFI, gases), and the ability to coordinate multiple vendor schedules simultaneously.
  • You have familiarity with reading and interpreting P&IDs, drawings, specifications also, reviewing turnover packages, vendor documentation.
  • You have familiarity with conducting or coordinating FAT and SAT testing
  • You love immersing yourself in difficult technical problems and coming up with solutions that work. You think outside the box and use your experience and intuition to identify when such solutions are realistic.
  • You have outstanding attention to detail as well as experimental and process rigour. You take pride in your work and strive for excellence.

The hiring range for this role is $94,000 - $102,000, annually. Our ranges are based on market data. Offered salaries will be based on a combination of factors including, but not limited to, job‑related knowledge, skills, education, and experience. For candidates who exceed role requirements, we are open to exploring above‑range offers. Note that base salary is just one part of the overall compensation at Aspect. Members of the Aspect team also receive equity, a comprehensive benefits package, and support for continuous learning and career progression.

At Aspect Biosystems, our strength has always been in our diversity. Different people, thinking differently, unified in creating a world that is better for us all. We are committed to creating an inclusive environment for everyone on our team. All aspects of employment — including the decision to hire, promote, discipline, or terminate — are based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, colour, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, provincial, or local law.

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