IT Manager Position Available In Wake, North Carolina

Tallo's Job Summary: IT System Manager (Consultant) position available with Technical Source in Raleigh, NC, offering a contract with an estimated salary of $75.3K - $89.2K a year. Ideal candidates possess a Bachelor's degree in Computer Science, 2 years of experience in IT system validation in regulated manufacturing environments, and expertise in Windows-based systems and QC software.

Company:
Technical Source
Salary:
JobFull-timeOnsite

Job Description

IT Manager Technical Source – 3.6

Raleigh, NC Job Details Contract Estimated:

$75.3K – $89.2K a year 2 days ago Qualifications Computer Science GMP Mid-level Windows Bachelor’s degree Quality control Organizational skills ServiceNow IT Manufacturing 2 years Information Technology Full Job Description Job Title IT System Manager (Consultant) – Pharma Manufacturing IT Systems | Biopharma Crescent, NC Job Overview Technical Source is currently in search of an IT System Manager (Consultant) to support one of our key pharmaceutical manufacturing clients in the greater Raleigh, NC area.

This critical role ensures lifecycle management, compliance, and operational excellence across regulated IT systems. The successful candidate will collaborate with stakeholders across the Quality, Production Support, and Automation teams to drive reliable, validated IT solutions supporting manufacturing and quality control (QC) operations. This is a 6-12 month contract role with potential for long-term value-add expansion as the facility scales operations. Responsibilities of the IT System Manager include: Manage IT systems across their full lifecycle, including documentation, validation, and decommissioning. Ensure systems meet internal SOPs, 21 CFR Part 11, GxP, and other regulatory requirements. Review and maintain Computer System Validation (CSV) documentation including FAT, SAT, IQ, OQ, and PQ. Configure software, user groups, access controls, and document system architectures. Provide escalation support, system troubleshooting, and ensure business continuity planning. Lead or support IT-related audits and deviation investigations in QC systems. Maintain system documentation (e.g., manuals, Servicenow entries, configuration baselines). Approve and maintain user access control processes and collaborate with IT Security. Mentor team members and assist in documentation reviews and training efforts. Coordinate support agreements and serve as a liaison for external/internal IT support. Execute IT-related project activities on agreed timelines. Qualifications of the IT System Manager include: Bachelor’s Degree in Computer Science, Information Technology, or a related field. 2-5 years of experience in the pharmaceutical industry, ideally within regulated manufacturing environments. Minimum of 3 years of experience in IT system validation, particularly within a GxP context. Hands-on experience with Windows-based environments and standalone QC software. Strong documentation skills and knowledge of SOP authoring, validation lifecycle, and system compliance. Ability to manage complex timelines, troubleshoot IT issues, and lead stakeholder communications. Strong organizational skills and comfort working in hybrid technical/regulatory environments.

Work Schedule & Contract Details:
Location:
Onsite Schedule:

Monday – Friday, standard business hours

Duration:

6-12 months (initial contract)

Start Date:

June 2025

Hourly Pay Rate:

Commensurate with experience (W-2 only)

Key Words:

IT System Manager, CSV, Validation, GMP, QC Software, Pharma IT, GxP, Windows, Compliance, SOPs, Data Integrity, Lifecycle Management, System Configuration

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