Division Quality Engineer
Job in
Durham, Durham County, North Carolina, 27703, USA
Listed on 2026-06-28
Listing for:
Corning Incorporated
Full Time
position Listed on 2026-06-28
Job specializations:
-
Quality Assurance - QA/QC
-
IT/Tech
Job Description & How to Apply Below
Division Quality Engineer I
Date:
Jun 24, 2026
Location:
Corning, NY, US;
Tewksbury, MA, US;
Durham, NC, US
Company:
Corning
Requisition Number: 75993
Role PurposeThis role ensures GxP computerized systems used across Corning Life Sciences remain compliant, validated, and fit for use throughout their lifecycle. It supports system validation, implementation, maintenance, and data integrity through risk-based approaches, while partnering with cross-functional teams to drive standardized, audit-ready validation practices aligned with regulatory and business requirements.
Key Responsibilities- Support the standardization of computer systems validation procedures, templates, and documentation practices across division manufacturing and laboratory facilities
- Support implementation and maintenance of validated computerized systems to ensure compliant, reliable, and available systems that support product quality and business continuity
- Author, review, execute, and approve CSV lifecycle documentation, including
- Ensure computerized systems remain in a validated state through effective management of
- Participate in system risk assessments and help define validation strategies based on system complexity, intended use, GxP impact, and regulatory expectations
- Support data integrity assessments and compliance activities aligned with applicable requirements for electronic records, electronic signatures, audit trails, system access, backup/recovery, and security administration
- Partner with IT, Automation, Quality, Engineering, and system owners to support implementation, qualification, and lifecycle management of systems such as
- Support supplier assessment and qualification activities for software vendors, service providers, and third‑party system integrators as required
- Participate in internal, customer, and third‑party audits and inspections, and support audit readiness for computerized systems compliance
- Support investigations, root cause analysis, and remediation efforts related to system issues, nonconformances, and validation gaps
- Drive continuous improvement in CSV processes, validation efficiency, template standardization, and inspection readiness
- Support new system implementations and upgrades, including validation impact assessments, test strategy development, and release to operational use
- Leverage risk-based validation methodologies and applicable lifecycle frameworks to support compliant and efficient validation activities
- Provide technical guidance to cross‑functional team members on CSV requirements, system compliance expectations, and validation deliverables
- Support the creation and maintenance of technical documentation that meets business needs and complies with applicable international standards and regulatory requirements (e.g. FDA, EU, ISO, GAMP, ALCOA+)
- Ensure validation deliverables are inspection‑ready, accurate, complete, traceable, and aligned with internal quality system requirements
- Lead CSV projects of moderate scale and complexity
- Participate in and sometimes lead validation activities on larger‑scale system implementation or remediation projects
- Some travel is required as part of the job responsibilities
- Bachelor’s degree in a technical or scientific field
- 1–2 years of experience in CSV, quality, IT systems, or regulated environments
- Working knowledge of GxP and validation lifecycle (IQ/OQ/PQ)
- Understanding of risk‑based validation and data integrity (ALCOA+)
- Familiarity with change control, deviations, CAPA, and audit readiness
- Exposure to systems such as ERP, LIMS, MES, SCADA, or eQMS
- Strong attention to detail and technical documentation skills
- Analytical thinker with problem‑solving and risk‑based decision‑making ability
- Effective communicator with strong collaboration skills
- Able to manage multiple tasks and work independently
- Life Science or Pharmaceutical Packaging product application knowledge and experience.
- Injection Molding manufacturing process knowledge and experience.
- Certified Quality Engineer recognition by ASQ.
- Certified Green or Black Belt recognition by ASQ.
This position does not support immigration sponsorship.
The range for this position…
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