Engineer, IT Shared Services
$83,680–$101,404 year
On-siteBothell, Washington, United States
Job Summary
Own and manage the IT shared landscape across the Cell Therapy site, including IT Architecture, Infrastructure, Networks, Servers, HMIs, Printers, Scanners, Switches, Firewall rules, and Domains. Serve as the CTF IT Cybersecurity Point of Contact, owning system patching efforts and monitoring ServiceNow tickets to reduce infrastructure incidents. Manage spares and inventory for IT Infrastructure while supporting Disaster Recovery as the main POC for P1 and P2 tickets. Ensure uninterrupted 24/7 operation of manufacturing systems for CAR-T Manufacturing. Requires a Bachelor's degree in engineering or MIS, 4+ years of hands-on experience in biotech manufacturing, and knowledge of cGMP, GDP, and 21CFR part 11. Location: Bothell, WA. Salary: $83,680 - $101,404.
Required Qualifications
- Bachelor's degree in an engineering or MIS discipline
- Experience with Cybersecurity, patching and IT Life Cycle Management (LCM) in a bio-tech manufacturing environment
- 4+ years of hands-on experience in a biotech manufacturing and supply chain environment
- Understanding of supply chain, manufacturing domains, and supporting technology including manufacturing and supply chain ERP systems (e.g., Oracle, SAP)
- Working knowledge of regulatory requirements and how they relate to existing and new business systems and practices, primarily GDPs
- Sound understanding of a Cell Therapy manufacturing facility IT Architecture and IT Infrastructure including Networks, Servers, HMIs, Printers, Scanners, Switches, Firewall rules, Domains, etc.
- Ability to effectively communicate with both technical and non-technical team members
- Strong interpersonal skills, especially regarding: Teamwork and collaboration
- Client focus
- Verbal and written communication
- Knowledge of Cell Therapy Facility (CTF) IT Architecture and IT Infrastructure including Networks, Servers, HMIs, Printers, Scanners, Switches, Firewall rules, Domains, etc.
- Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, and good documentation practices
- Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment that support Biologics and clinical manufacturing
- Strong technical and problem-solving skills and the ability to work independently
- Demonstrated success working in a high-performing, business results-driven environment
- Knowledge of Cybersecurity, patching and IT Life Cycle Management (LCM)
- Understanding of computer system validation
- 100% of shifts onsite at your assigned facility
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