MES Engineer

Validation & Engineering Group; Morrisville (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

A leading engineering services firm is seeking a Senior Computer System Validation Specialist in Morrisville, NC. This role involves leading validation activities for Manufacturing Execution Systems, specifically Syncade, ensuring compliance with FDA and other regulations. Candidates should have 7-10+ years in computer validation within a GMP-regulated environment, expertise in MES, and strong technical writing skills. This position offers a dynamic role in a growing biopharmaceutical facility, contributing to high-quality manufacturing processes.

Qualifications

• 7–10+ years of experience in Computer System Validation within GMP-regulated biologics or pharmaceutical manufacturing.
• Hands-on expertise with MES Syncade validation and configuration.
• Excellent technical writing and documentation skills.

Responsibilities

• Lead and execute CSV activities for MES in a biologics GMP environment.
• Develop and maintain validation documentation.
• Provide audit support during regulatory inspections.

Skills

MES Syncade validation

Technical writing

Problem-solving

Leadership

Communication

Education

Bachelor’s degree in Engineering, Computer Science, Life Sciences or related field

Advanced degree

Tools

TrackWise

Veeva

ValGenesis

Kneat

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

Job Description

Senior Computer System Validation (CSV) Specialist - with expertise in Manufacturing Execution Systems (MES), specifically Syncade, to support a biologics manufacturing facility. The role will be responsible for planning, authoring, executing, and reviewing validation deliverables in compliance with FDA, EMA, ICH, and GAMP 5 guidelines. The candidate will work closely with Quality, IT, Engineering, and Manufacturing teams to ensure validated, compliant, and reliable MES system operation throughout the system life cycle.

Key Responsibilities

• Lead and execute CSV activities for MES (Syncade) in a biologics GMP environment.
• Develop and maintain validation documentation including Validation Plans, User Requirements (URS), Functional Specifications (FS), Design Specifications (DS), Risk Assessments, IQ/OQ/PQ protocols, and summary reports.
• Partner with Manufacturing and Quality to ensure MES recipes, workflows, and master batch records are validated and compliant.
• Perform impact assessments and change control for system upgrades, patches, and enhancements.
• Ensure alignment of CSV deliverables with GAMP 5, 21 CFR Part 11, Annex 11, and other applicable regulations.
• Collaborate with IT and Engineering teams for system integration (e.g., LIMS, ERP/SAP, DeltaV, PI Historian).
• Provide audit support during regulatory inspections (FDA, EMA, MHRA, etc.) and customer audits.
• Mentor junior validation engineers and support knowledge transfer on CSV best practices.
• Contribute to continuous improvement of MES validation strategies, procedures, and templates.

Qualifications

Qualifications

• Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field. Advanced degree preferred.
• 7–10+ years of experience in Computer System Validation within GMP-regulated biologics/pharmaceutical manufacturing.
• Hands‑on expertise with MES Syncade validation and configuration (recipes, workflows, batch records).
• Strong knowledge of regulatory guidelines: FDA 21 CFR Part 11, EU Annex 11, ICH Q7, GAMP 5.
• Experience in biologics manufacturing processes (cell culture, purification, fill/finish).
• Familiarity with integration points (DCS/DeltaV, LIMS, ERP/SAP, data historians).
• Excellent technical writing and documentation skills.
• Strong communication, leadership, and problem‑solving abilities.

Preferred Skills

• Experience in large‑scale biotech/biologics start‑up or tech transfer projects.
• Knowledge of data integrity principles and ALCOA+ requirements.
• Exposure to quality management systems (TrackWise, Veeva, ValGenesis, Kneat).
• Understanding of 21st Century Cures Act and CSA (Computer Software Assurance) approaches.

Additional Information

All your information will be kept confidential according to EEO guidelines.