Why This Role Stands Out
This on-site role offers a competitive hourly rate and the chance to contribute to critical GMP lab computing systems, fostering your expertise in a reputable consulting environment. You'll thrive here if you have strong experience with GMP laboratory systems and a commitment to ensuring compliant and reliable operations. Apply now to grow your career in this impactful position.
Quick Overview
Job Description
Job Title: IT Lab Computing Support Specialist
Location: Bothell, WA - onsite
Duration: 12 months + potential to extend
Pay Range: $38/hr - $48/hr (W2)
Work Schedule: Initial shift 8 a.m.-4 p.m. for one month. Training shift 11 a.m.-7 p.m. for one month. Ongoing shift 3 p.m.-11 p.m.
About TSR
TSR is a trusted staffing and workforce solutions partner with more than 50 years of experience delivery highly qualified talent to support clients' most critical business and technology initiatives. Through a disciplined approach to sourcing, candidate vetting, and delivery, TSR helps organizations scale teams quickly while maintaining quality and reliability. TSR operates with a global delivery model, leveraging specialized teams to support enterprise clients across North America and beyond.
In June 2024, TSR was acquired by Justin Christian, founder and CEO of BCforward, a global provider of professional services and workforce solutions. This partnership expands TSR's ability to deliver broader capabilities, global delivery resources, and enhanced opportunities for both clients and consultants.
Job Description
We are seeking a GMP Lab Computing Services (LCS) Engineer to join our team. The ideal candidate will have strong experience in GMP laboratory computerized systems, laboratory applications, instrumentation interfaces, and supporting infrastructure and a proven ability to maintain compliant, reliable operations and lead lifecycle activities through controlled technical execution.
Responsibilities:
- Provide senior-level ownership and support for GMP laboratory computing systems and services.
- Maintain reliable operation of applications, computerized systems, workstations, instruments, interfaces, and infrastructure.
- Lead troubleshooting, incident response, and coordination across technical and business teams.
- Execute lifecycle activities including implementation, configuration, maintenance, upgrades, and decommissioning with complete documentation.
- Perform work in accordance with GMP, SOPs, work instructions, and quality processes using a risk-based approach.
- Assess, plan, and verify changes through approved change control with acceptance criteria and rollback strategies.
- Develop and execute risk-appropriate testing, verification, and support for CSV/CSA activities with complete evidence.
- Apply data-integrity controls for electronic records, access, audit trails, configurations, interfaces, and data flows.
- Lead incident, deviation, and investigation support with root-cause analysis and CAPA verification.
- Create and maintain accurate technical documentation and configuration records following Good Documentation Practices.
- Mentor engineers, establish consistent engineering practices, and promote accountability and continuous improvement.
Required Skills & Qualifications:
- Bachelor's in Computer Science, Engineering, Information Technology, Life Sciences, or related field, or equivalent experience.
- Significant experience supporting laboratory computing and regulated computerized systems in GMP environments.
- Strong knowledge of GMP principles, Good Documentation Practices, and controlled technical execution.
- Proven troubleshooting and analytical problem-solving abilities across applications, instruments, and infrastructure.
- Experience with change management, testing, verification, and full system lifecycle support.
- Experience collaborating with Quality, Laboratory Operations, Engineering, Cybersecurity, Infrastructure, and vendors.
- Clear technical writing and communication skills with sound technical judgment and independence.
Preferred Skills:
- Background in pharmaceutical, biotechnology, medical device, or other highly regulated laboratories.
- Experience with CSV or CSA, laboratory informatics, and instrument-to-system interfaces.
- Knowledge of Windows-based laboratory environments, virtualization, networking, databases, and enterprise interfaces.
- Experience with data-integrity assessments, change control, deviations, CAPA, and audits or inspections.
- Project leadership and mentoring experience.
Why TSR?
At TSR, we believe in advancing lives and careers. When you join our team, you gain access to:
- Competitive compensation and benefits.
- Opportunities for growth with global clients.
- A supportive, inclusive culture that values innovation and people.
- Exposure to cutting-edge technologies and projects.
About Our Commitment
TSR is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, or veteran status.
Interested? Apply Now!
If this sounds like the right opportunity for you, please apply with your most recent resumes
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