My name is Sibin, and Iama Recruiter with The Fountain Group. We are a staffing firm and are currently seeking Technical Consultantfor a prominent client of ours. This position is located in Lexington, MA. Details of the position are as follows:
- Type: Onsite
- Location: 300 Shire Way, Lexington, MA 02421
- Pay: $85+/hr on W2
- Duration: 12 months with potential extension
- Target Start Date: 10/19/2026
- LinkedIn ID required
- W2 candidates only
Job Description
- Provide hands-on IT application support and first-line triage for QC laboratory and manufacturing systems in a GxP/GMP environment.
- Troubleshoot application, workstation, laboratory equipment, and system issues and coordinate repair activities when equipment is down.
- Manage Incident, Change, Problem, Asset, and Configuration requests through ServiceNow.
- Perform validation activities including backup/restore testing, user access reviews, audit trail reviews, patching, and system decommissioning.
- Support application implementations, upgrades, and Windows workstation migrations.
- Develop and maintain SDLC/validation documentation including SDCS, URS, FRA, IQ, IOQ, ATR, SOPs, and application data flow diagrams.
- Support vendor-provided solutions and technical requests across QC, laboratory, validation, and product development functions.
- Work within regulated environments requiring GMP/GxP procedures, SOPs, data integrity controls, and controlled access.
Education
- Bachelor’s degree in Information Technology, Computer Science, Engineering, Business Administration, or related field preferred.
- Equivalent technical experience accepted.
Required Skills
- 3+ years of relevant IT/application support experience; 5+ years preferred.
- Hands-on application and systems support within a GxP/GMP environment.
- QC laboratory and analytical instrumentation support.
- Technical triage and end-to-end ticket management.
- Computerized Systems Validation (CSV).
- 21 CFR Part 11 and data integrity compliance.
- ServiceNow Incident, Change, Problem, Asset, and Configuration Management/CMDB.
- Windows Desktop/Server, Active Directory, Group Policy, LDAP, NTFS permissions, TCP/IP, RDP, and backup/restore.
- Validation and SDLC documentation: SDCS, URS, FRA, IQ, IOQ, ATR, SOPs.
- Microsoft Word/Office 365 and technical documentation.
- Laboratory application support involving systems such as Empower, Chromeleon, LabX, Veeva, TrackWise, or comparable GxP applications.
Preferred Skills
- Experience supporting QC laboratory instruments such as Roche Cedex, Roche LightCycler 480, Nova Biomedical BioProfile, Lonza WinKQCL, PerkinElmer Asset Genius, Thermo TruScan RM Analyzer, Waters systems, or comparable equipment.
- Veeva document workflows and TrackWise CAPA, deviation, and change control.
- SCADA, PLC, DCS, historian, or laboratory automation systems.
- SQL databases, Citrix, server virtualization, firewall rules, and cloud/on-premise architectures.
- Experience with pharmaceutical, biotechnology, or life sciences environments.
- MS Visio and MS Project.
- GxP workstation patching, application upgrades, decommissioning, and vendor solution implementation.