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Laboratory Support Engineer

Job in Spring House, Montgomery County, Pennsylvania, 19477, USA
Listing for: Eurofins USA PSS Insourcing Solutions
Full Time position
Listed on 2026-07-24
Job specializations:
  • IT/Tech
    Systems Engineer, IT Support
Salary/Wage Range or Industry Benchmark: 90000 - 115000 USD Yearly USD 90000.00 115000.00 YEAR
Job Description & How to Apply Below
Location: Spring House

Job Description

We have an exciting opportunity for a Laboratory Operations Engineer to join a growing team at a PSS Client site. The Laboratory Operations Engineer will be responsible for supporting process systems in clinical and non-clinical Regulated Bioanalytics laboratories. This position may provide direct support to automation asset maintenance, system security, data management, obsolescence initiatives and all SDLC and Compliance needs.

Job Duties Include
  • Collaborate with divisional/enterprise Information teams, global infrastructure, and risk/security organizations to ensure compliant laboratory support of regulated bioanalytical laboratory programs
    • Support the lifecycle of GxP equipment including the acquisition, installation, maintenance, and retirement phases.
    • Apply deep expertise in the computer system validation process for diverse laboratory equipment such as automated liquid handlers, plate readers, and PCR systems.
    • Maintain service schedules for instrument maintenance, ensuring timely completion of calibration and maintenance activities in accordance with departmental SOPs.
    • Coordinate service activities involving various vendors, service engineers, and facilities staff, fostering strong professional relationships.
    • Develop a working knowledge of laboratory equipment, like liquid handlers, plate washers/readers, and PCR.
    • Serve as system administrator for equipment applications, including temperature monitoring systems, assisting in the management of controlled temperature units and alarm handling.
    • Collaborate with lab ops staff across bioanalytical labs and sites for process improvement, cross-training and cross-site support.
    • Engage in the routine operations supports promoting a culture of continuous improvement.
    • Assist in the development of reporting, analytics and visualization solutions to support local clinical operations and administrative business processes.
  • Ensuring automation systems are maintained in a validated state, as part of an active/ongoing lifecycle management program and in compliance with current GXP requirements.
    • Reviewing documents, preventive maintenance, and Standard Operating Procedures to ensure compliance with GxP Practice and corporate safety requirements.
    • Enhance the existing LAMP infrastructure to track equipment preventative maintenance (PM) within the client’s department.
    • Provide compliance support activities such as entering PM and corrective maintenance services in the electronic laboratory logbook.
    • Oversee outsourced pipette calibration, maintaining records in the electronic logbook. Generate and review out-of-calibration impacts reports, share it with management and take appropriate actions.
    • Perform Hamilton verification after PM/CM, documenting verification in the electronic logbook.
    • Utilize technical knowledge to ensure efficient operation of various automated processing and informational technology systems.
    • Participate in compliance audits and training programs.
    • Providing client services support for business area laboratory applications.
Safety Considerations
  • May come into contact with potentially infectious material.
  • May handle hazardous chemicals.
  • This site is not accessible by public transportation options; daily, reliable transportation is needed to and from the site.
Qualifications
  • Minimum of a Bachelor of Science degree needed (with a minimum of 2 years of relevant experience) or a Master’s degree in engineering science, Information Technology or a related field.
  • Authorization to work in the country indefinitely without sponsorship.
Required Skills
  • Experience in a GLP or GMP laboratory, preferably in a bioanalytical setting.
    • Proven experience in validation activities and associated Quality functions.
    • Demonstrated strong interpersonal skills with the ability to influence others and promote a culture of inclusion, feedback, and empowerment.
    • Highly organized, and multitasking capabilities to manage multiple equipment or system schedules, documents, and maintenance tasks.
    • Strong verbal and written communication skills, with comfort in interacting with diverse on-site and off-site collaborators.
    • Ability to follow Standard Operating Procedures with insight into…
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