Lab PC and System Engineer -Pharma Industry

Westbourne; Foster City (CA); On-site; USD 85,000 - 125,000; Full time

Job summary

Westbourne is seeking a Lab PC engineer to join Lab IT services at the client site in California. The role focuses on deploying IT projects in pharmaceutical GxP lab environments.

The engineer will handle system requirements, hardware procurement, OS/app installs, and SOP updates while ensuring GMP compliance and security controls. This is a hands-on position requiring 3–5 years in pharma IT labs.

Qualifications

• Experience in pharma QC labs and GxP environments.
• Proven ability to install/configure hardware and OS.
• 3–5 years working in pharma/IT labs.

Responsibilities

• Understand system requirements and design solutions for pharma GMP standards.
• Install and configure applications per specifications.
• Manage platform upgrades and SOP updates.
• Author / update requirements and change requests (CR).
• Procure and build hardware, image and deploy systems.
• Provide testing support and assist script execution.
• Coordinate security/audit activities per client policy.
• Resolve issues escalated by the support desk.

Skills

GxP Lab

Pharma QC Lab

Windows Admin

Education

Bachelor of Science in Computer Science

Job description

Requirement

We are currently looking to hire a Lab PC engineer to join our Lab IT services at the client site. The engineer will have experience of successfully deploying IT projects in pharmaceutical GxP Lab environments

Requirement

We are currently looking to hire a Lab PC engineer to join our Lab IT services at the client site. The engineer will have experience of successfully deploying IT projects in pharmaceutical GxP Lab environments

Main Responsibilities

• Understand System Requirements, Design system solution consistent with pharma GMP Standards
• Install and Configure Applications per specifications
• Manage platform upgrades
• Author requirements documents (e.g., user, functional) , Contribute to configuration specifications
• Author server Technical Requirements Specification, Author / Update Standard Operating Procedures (SOPs)
• Contribute to testing procedures, Assist with Script Execution, Author Change Request (CR)
• Procure and build hardware, Image and deploy systems
• Decommissioning
• Resolve issues escalated by sustain support desk.

IT Compliance Tasks

• Security and Audit Trail Review. Assessment of data generation, modification and deletion, auditable events date and time stamps. Modifications to metadata, sample data sets. Identification and follow up on remediation activities following security and audit trail review.
• Windows 10 security patch update, Reboot and perform system verification check as per client procedures. Scheduled checks following Windows 10 Security Patch, quarterly updates, with execution/implementation planned by month

Industry Experience Required

• Experience working in pharmaceutical QC Lab environment, Min 3 years in Pharma
• Experience Installing, configuring, and troubleshooting computer hardware, operating systems, applications, and network issues in a GxP and non GxP environment. 3-5 years

Education And Skills

• Bachelor of Science in Computer Science or equivalent