What are the responsibilities and job description for the LIMS Support Specialist position at PharmEng Technology?
About the job LIMS Support SpecialistLIMS Support Specialist Quality Control (QC)
Onsite | Swiftwater, PA
Consulting or Full-Time Opportunity
We are seeking a LIMS Support Specialist to provide hands-on support to the Quality Control (QC) department. This role involves LIMS configuration, master data governance, and project support activities aligned with GMP and regulatory requirements.
Key Responsibilities
LIMS Configuration & Technical Support
Onsite | Swiftwater, PA
Consulting or Full-Time Opportunity
We are seeking a LIMS Support Specialist to provide hands-on support to the Quality Control (QC) department. This role involves LIMS configuration, master data governance, and project support activities aligned with GMP and regulatory requirements.
Key Responsibilities
LIMS Configuration & Technical Support
- Customize and configure the LIMS platform to align with lab workflows, testing needs, and terminology.
- Modify standard software code or develop new code to meet unique lab requirements.
- Ensure user workflows, reports, and data elements are integrated without altering base code.
- Serve as the LIMS System Owner, managing system changes and upgrades.
- Build and support a master data governance model for vaccine product specifications and analytical testing.
- Ensure alignment with cGMP and data integrity requirements across QC instruments and systems.
- Manage and maintain master specification documents for commercial products.
- Oversee static master data for QC-LIMS, ensuring data accuracy, ownership, and semantic consistency.
- Support audit readiness, regulatory inspections, and compliance-driven documentation.
- Work closely with internal QC teams, IT development teams, and global stakeholders.
- Support the Data Logistics & Support (DLS) Department in meeting operational and project milestones.
- Lead and contribute to LIMS master data management efforts for analytical testing portfolios.
- Experience supporting or configuring LIMS platforms (LabWare, STARLIMS, or similar) in a GMP-regulated environment.
- Familiarity with QC laboratory workflows, analytical testing, and regulatory compliance.
- Strong understanding of master data governance and scientific data semantics.
- Proficient in LIMS system ownership, change control processes, and cross-department coordination.
- Excellent documentation, communication, and stakeholder engagement skills.