Position Summary:
This on-site role (based in Sanford, NC) supports and leads IT systems for Quality Control (QC) lab applications, especially LIMS (LabVantage) and related lab software. The person will configure, implement, and manage systems critical to biopharma manufacturing, with a focus on compliance, data integrity, and lab efficiency.
Key Responsibilities:
- Lead implementation, configuration, and support of QC IT systems: LIMS, ELN, and lab instrument software/integrations.
- Act as system administrator (user setup, security roles).
- Manage LIMS configurations for business-critical processes (e.g., environmental monitoring, CoA, stability testing).
- Support GxP validation, SDLC processes, and change control activities.
- Provide technical guidance and collaborate with QC, IT, and manufacturing teams.
- Troubleshoot, optimize, and document complex technical systems.
- Align IT solutions with business and compliance goals.
Requirements:
Education & Experience:
- Associate’s or Bachelor’s degree in IT or related field.
- 5+ years in IT support or system management.
- Experience in biopharma, GMP/GDP environments preferred.
- Background in IT project management and working with end-users.
Technical Skills:
- Expertise in LabVantage LIMS.
- Familiarity with ITIL, ITSM frameworks, system integration, security, and compliance.
- Strong system troubleshooting, documentation, and reporting skills.
Soft Skills:
- Excellent communication and interpersonal skills.
- Highly organized, detail-oriented, and adaptable to a fast-paced, evolving environment.
- Cultural sensitivity and teamwork across global teams.
Job sourced from Kyowa Kirin.