Lab Operations Engineer - Group Leader

Eurofins BioPharma Product Testing · Spring House, PA

Posted October 26, 2026

Mid levelEngineering and FacilitiesGMPGLPOn site
Pay not postedApply

Quick facts

Experience
2+ years
Education
Bachelor's or Master's
Job type
Full-time
Visa sponsorship
Not offered
Skills mentioned
GMP, GLP, Root cause analysis, Audits, SOP writing, Validation

Pulled from the ad below. The full ad has the details.

Job Description

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  • 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.

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  • 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.

Leadership Responsibilities

  • Act as a technical resource, trainer, and troubleshooter for the department
  • Make recommendations for operational and/or technical improvements
  • Communicate effectively within the group
  • Coach and develop direct reports
  • Plan and monitor workflows
  • Monitor and approve employees’ time worked through time-entry system
  • Support and promote company policies and procedures

The site is not accessible by public transportation routes/options.

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.
  • Previous leadership experience

Required skills

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  • 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 continuous improvement.
  • Apply general knowledge of company business developed through education or experience.
  • Understand and apply regulatory/ compliance requirements relative to the role.
  • Problem solver/troubleshooter, skilled in Root Cause Analysis (RCA).

Additional Information

Position is full-time, Mon-Fri 8am-5pm. Candidates currently living within a commutable distance of Spring House, PA are encouraged to apply. The site is not accessible by public transportation routes/options.

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Source: Eurofins BioPharma Product Testing's career site. PharmoniQ shows this job as posted and links to the original. Check the employer's page for the latest details.