IT Lab Systems Specialist

Pharmaron Beijing Co. Ltd.; West Whiteland Township (Chester County); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Health Insurance

401(k) Plan with employer matching

Paid Time Off

Job summary

Pharmaron seeks an IT Lab Systems Specialist to support and advance IT operations in a GMP-regulated laboratory. You will ensure that laboratory computer systems, connected instruments, and supporting infrastructure run securely, reliably, and in compliance with data integrity standards.

Based in Exton, PA, this on-site role collaborates with QA, Scientific Operations, and IT to manage validation, backups, and documentation, with occasional travel to U.S. labs.

Qualifications

• Bachelor's degree in IT or CS with 5–7 years of GMP/GLP IT in pharma/biotech.
• Strong knowledge of laboratory instruments and computerized systems.
• Experience with CSV, computer system validation, and regulatory documentation.

Responsibilities

• Provide IT support for laboratory instruments and computerized systems in a GMP environment.
• Coordinate maintenance, upgrades, and escalations with vendors.
• Develop and maintain SOPs and technical documentation for IT operations.

Skills

GxP compliance understanding

Regulated pharma IT environment

Laboratory IT systems experience

Cybersecurity principles

Windows-based environments

Education

Bachelor's degree in Information Technology or Computer Science

Tools

LIMS

LCMS

HPLC

Flow Cytometry

PCR platforms

Oracle

SQL Server

Job description

Position: IT Lab Systems Specialist

Salary Range: $75,000 - $95,000

Location: Exton, PA (On-site)

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services. We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.

What You'll Do

Reporting to the Director of IT, the IT Lab Specialist plays a critical role in supporting and advancing IT operations within a GxP-regulated laboratory environment. This position ensures that laboratory computer systems, connected instruments, and supporting infrastructure operate securely, reliably, and in full compliance with regulatory, quality, and data integrity standards. Working cross-functionally with Scientific Operations, Quality, and IT teams, the IT Lab Specialist supports system implementation, validation, lifecycle management, backup and recovery processes, and continuous improvement initiatives across laboratory technologies.

Key Responsibilities

• Provide hands-on IT support for laboratory instruments, applications, and computerized systems within a GxP-regulated environment Troubleshoot and resolve hardware, software, and network connectivity issues related to laboratory systems and instruments (e.g., Cell Counters, Flow Cytometers, LIMS, PCR systems)
• Partner with instrument and software vendors to coordinate maintenance, technical support, upgrades, and escalations
• Manage system backups, data integrity verification, and restore testing in accordance with internal policies and regulatory requirements
• Create and maintain technical system documentation for laboratory instruments, including hardware/software configurations, architecture, interfaces, and data flow mappings
• Author and maintain SOPs and technical documentation supporting laboratory IT operations, backup processes, and system administration activities
• Administer user accounts, access controls, and security permissions in alignment with established procedures and segregation of duties requirements
• Serve as the document owner for IT-related GxP procedures, including system administration, backup/restoration, and user management processes
• Support qualification and validation activities (IQ/OQ/PQ and CSV) for laboratory systems in collaboration with QA and external vendors
• Ensure compliance with 21 CFR Part 11, EU Annex 11, GDPR, EO 14117, and internal IT and quality standards
• Lead and support change control activities, including impact assessments, risk evaluations, testing coordination, and approval documentation for system updates and configuration changes
• Perform periodic reviews of computerized systems, including patch management, audit trail reviews, and lifecycle assessments
• Support laboratory system upgrades, integrations, and migrations involving enterprise platforms such as LIMS and ELN
• Participate in internal and external audits as the subject matter expert (SME) for laboratory IT systems and infrastructure
• Train and support laboratory personnel on IT procedures, system usage, data handling, and cybersecurity best practices
• Collaborate with cross-functional IT teams to ensure operational continuity and timely resolution of technical issues across laboratory and business systems
• Occasional travel to U.S. laboratory and CGT sites may be required

What We're Looking For

• Bachelor's degree in Information Technology, Computer Science, or a related discipline 5–7 years of IT experience within GMP, GLP, or other regulated pharmaceutical or biotechnology environments
• Strong knowledge of laboratory instruments and computerized systems, including LIMS, LCMS, HPLC, Flow Cytometry, and PCR platforms
• Deep understanding of GxP compliance, data integrity principles, and regulated documentation practices
• Hands-on experience with Windows-based environments, backup and recovery technologies, and basic network infrastructure
• Experience administering databases such as Oracle and SQL Server
• Knowledge of cybersecurity principles and controls within regulated environments
• Familiarity with computer system validation (CSV), SDLC methodologies, and risk-based system assessments
• Strong analytical, organizational, and communication skills with the ability to work effectively across technical and scientific teams

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture

You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits

• Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
• 401(k) Retirement Plan with generous employer matching
• Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
• Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
• Employee Assistance Program (EAP), mental health resources, and wellness programs
• Family-friendly benefits, including fertility support and maternity resources
• Professional development and career growth opportunities within a leading global CRO/CDMO

As an Equal Employment Opportunity and Aff

#LI-KS1