TECH SVCS GMP Lab Computing Services (LCS) Engineer
Job Location:
Bothell, WA - USA
Hourly Salary:
USD 49 - 52
Posted:
29 September 2026 (16 hours ago)
Application Deadline:
27 December 2026
Vacancies:
1 Vacancy
Job Summary
GMP Lab Computing Services (LCS) Engineer
Job Number: 26-01597
Job Number: 26-01597
Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a GMP Lab Computing Services (LCS) Engineer for our client in Bothell WA.
ECLAROs client is a leader in the Biopharmaceutical Industry providing quality innovative and affordable medicines that make a difference in the lives of patients all over the world. If youre up to the challenge then take a chance at this rewarding opportunity!
Position Overview:
- The GMP Lab Computing Services (LCS) Engineer is a technical role responsible for the reliable compliant and lifecycle management of laboratory computing systems and associated technologies supporting GMP-regulated laboratory operations.
- This role provides technical support for laboratory computerized systems infrastructure instrumentation interfaces applications and associated services throughout their lifecycle.
- The position requires a strong combination of laboratory computing expertise engineering discipline GMP knowledge quality mindset and operational ownership.
- The LCS Engineer is expected to operate beyond traditional IT support.
- The role requires the engineer to understand the business and laboratory requirements assess risk execute controlled technical activities verify outcomes maintain complete documentation and ensure systems remain in a compliant and validated/qualified state as applicable.
- The position works closely with Laboratory Operations Quality Assurance Engineering Facilities Cybersecurity Infrastructure Service Management vendors and other stakeholders to ensure laboratory computing services are reliable secure supportable and compliant.
Responsibilities:
- Laboratory Computing Services:
- Provide senior-level technical support and ownership for GMP laboratory computing systems and associated services.
- Maintain reliable operation of laboratory applications computerized systems workstations instruments interfaces and supporting infrastructure.
- Serve as a technical subject matter expert for assigned laboratory computing platforms and services.
- Lead troubleshooting of complex technical issues and coordinate resolution across multiple technical and business teams.
- Provide technical direction during system incidents service interruptions and complex operational events.
- Develop sustainable solutions to recurring technical problems and reduce operational risk.
- Support laboratory system lifecycle activities including implementation configuration maintenance upgrades retirement and decommissioning.
- Maintain appropriate technical documentation system information configuration records and support procedures.
- GMP and Quality:
- Perform all activities in accordance with applicable GMP requirements company policies SOPs work instructions and quality processes.
- Apply a risk-based approach to laboratory computing activities.
- Understand how changes to computerized systems may affect laboratory operations product quality data integrity and regulatory compliance.
- Ensure technical activities are appropriately planned controlled executed verified and documented.
- Recognize when a technical activity requires change control validation/assurance deviation management Quality review or additional approval.
- Promote a culture in which quality is embedded into technical execution rather than treated as a post-implementation activity.
- Demonstrate willingness to stop work and escalate when requirements procedures system state or expected results are unclear or inconsistent.
- Support internal and external regulatory inspections and audits as a technical subject matter expert.
- Computerized System Lifecycle:
- Provide technical leadership throughout the lifecycle of GMP computerized systems.
- Participate in system planning requirements definition design configuration testing implementation maintenance upgrades and retirement.
- Ensure system configurations remain aligned with approved requirements and intended use.
- Maintain awareness of system dependencies interfaces data flows infrastructure and upstream/downstream impacts.
- Support lifecycle documentation and ensure technical records remain current.
- Identify obsolete unsupported or high-risk technologies and develop appropriate remediation strategies.
- Support system lifecycle roadmaps and technology modernization initiatives.
- Change Control and Risk Management:
- Lead or provide technical ownership for changes affecting laboratory computerized systems.
- Assess technical operational GMP and data-integrity impacts of proposed changes.
- Develop appropriate implementation testing verification and rollback strategies.
- Ensure changes are implemented according to approved plans.
- Confirm that completed changes achieve predefined acceptance criteria before considering work complete.
- Provide technical input to risk assessments and determine appropriate controls based on system and business risk.
- Ensure appropriate objective evidence is generated and retained.
- Verification Testing and Validation/Assurance:
- Develop and execute technical testing and verification activities appropriate to the risk and intended use of the system.
- Ensure acceptance criteria are established before execution.
- Review expected versus actual results and investigated unexpected outcomes.
- Provide technical support for validation qualification or computerized assurance activities as applicable.
- Ensure test evidence is complete accurate traceable and attributable.
- Support independent review of critical technical activities where required.
- Partner with CSV/CSA and Quality organizations to ensure appropriate lifecycle controls are applied.
- Recognize that successful technical execution does not constitute completion until required verification and documentation are complete.
- Data Integrity:
- Apply data-integrity principles to laboratory computerized systems and associated services.
- Understand controls associated with electronic records user access audit trails system configurations interfaces and data flows.
- Ensure technical activities do not compromise the integrity availability or traceability of regulated data.
- Support assessment and remediation of data-integrity risks.
- Escalate suspected data-integrity issues promptly and appropriately.
- Ensure system access and configuration activities are performed according to approved procedures and segregation-of-duty requirements.
- Incident Deviation and Investigation Support:
- Provide technical leadership for complex incidents affecting GMP laboratory systems.
- Support deviation and nonconformance investigations.
- Develop technically sound problem statements and event timelines.
- Gather and preserve appropriate technical evidence.
- Participate in root-cause analysis and impact assessments.
- Develop corrective and preventive actions where appropriate.
- Ensure technical remediation is verified for effectiveness.
- Identify recurring issues and drive systemic improvements rather than repeated temporary fixes.
- Documentation and Good Documentation Practices:
- Create and maintain clear accurate complete timely and traceable technical documentation.
- Follow applicable Good Documentation Practices and data-integrity requirements.
- Ensure documentation accurately reflects work actually performed.
- Maintain system configuration records technical procedures support documentation testing evidence and change records.
- Ensure technical records allow reconstruction of what was performed by whom when and with what result.
- Identify and correct documentation deficiencies through appropriate quality processes.
- Technical Support and Mentoring:
- Serve as a technical leader and subject matter expert within the LCS organization.
- Mentor engineers and technical staff in laboratory computing GMP quality troubleshooting and controlled execution.
- Establish and promote consistent engineering practices across the team.
- Coach engineers to think beyond task completion and focus on verification documentation and risk.
- Review technical approaches and provide guidance on complex issues.
- Build technical depth and redundancy within the LCS organization.
- Support development of engineering standards procedures troubleshooting guides and knowledge-management practices.
- Help establish a culture of accountability ownership and continuous improvement.
- Continuous Improvement:
- Identify opportunities to improve laboratory system reliability service quality compliance and operational efficiency.
- Use incident service and system data to identify recurring problems and systemic weaknesses.
- Drive automation and standardization where appropriate without compromising GMP controls.
- Reduce unnecessary manual processes and operational dependencies.
- Develop strategies to improve system availability supportability and lifecycle sustainability.
- Contribute to long-term laboratory computing technology roadmaps.
Required Qualifications:
- Bachelors degree in computer science Computer Engineering Electrical Engineering Information Technology Life Sciences or related technical discipline; equivalent relevant experience may be considered.
- Significant experience supporting laboratory computing computerized laboratory systems scientific systems instrumentation or related technologies.
- Demonstrated experience working within a GMP-regulated environment.
- Strong understanding of GMP principles and Good Documentation Practices.
- Demonstrated experience with controlled technical execution change management testing and verification.
- Strong troubleshooting and analytical problem-solving skills.
- Experience supporting regulated computerized systems throughout their lifecycle.
- Experience working with cross-functional teams including Quality Laboratory Operations Engineering Cybersecurity Infrastructure and vendors.
- Strong technical writing and communication skills.
- Demonstrated ability to work independently and exercise sound technical judgment.
- Ability to balance operational urgency with GMP and quality requirements.
- Technical Excellence: Demonstrates advanced knowledge of laboratory computing technologies and can independently troubleshoot complex systems and infrastructure.
- GMP and Quality Mindset: Understands that quality is part of technical execution and consistently incorporates GMP data integrity risk management verification and documentation into daily work.
- Ownership and Accountability: Takes end-to-end ownership of technical problems and ensures that issues are resolved verified documented and appropriately closed.
- Risk-Based Decision Making: Considers technical operational compliance data-integrity and business risks before making decisions or implementing changes.
- Communication: Clearly communicates technical issues risks decisions and recommendations to both technical and non-technical stakeholders.
- Collaboration: Builds effective relationships across LCS Laboratory Operations Quality CSV/CSA Engineering IT Cybersecurity and other organizations.
- Continuous Improvement: Identifies opportunities to improve reliability efficiency standardization compliance and user experience.
Preferred Qualifications:
- Experience supporting pharmaceutical biotechnology medical device or other highly regulated laboratory environments.
- Experience with computerized system validation (CSV) or computer software assurance (CSA).
- Experience with laboratory informatics and laboratory applications.
- Experience supporting laboratory instruments and instrument-to-system interfaces.
- Experience with Windows infrastructure supporting laboratory systems.
- Experience with virtualization networking databases system interfaces or enterprise infrastructure.
- Experience with data-integrity assessments.
- Experience with change control deviation investigations CAPA and risk assessments.
- Experience supporting regulatory inspections or audits.
- Experience leading technical projects or system implementations.
- Experience mentoring engineers or technical staff.
Pay Rate: $49.62-$52.62/Hour
If hired you will enjoy the following ECLARO Benefits:
- 401k Retirement Savings Plan administered by Merrill Lynch
- Commuter Check Pretax Commuter Benefits
- Eligibility to purchase Medical Dental & Vision Insurance through ECLARO
If interested you may contact:
Paul Quibuyen
Paul Quibuyen LinkedIn
Equal Opportunity Employer:ECLARO values diversity and does not discriminate based on Race Color Religion Sex Sexual Orientation National Origin Age Genetic Information Disability Protected Veteran Status or any other legally protected group status in compliance with all applicable laws.
Required Experience:
IC
About Company
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