Company 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
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Lead and execute CSV activities for MES (Syncade) in a biologics GMP environment.
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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.
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Partner with Manufacturing and Quality to ensure MES recipes, workflows, and master batch records are validated and compliant.
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Perform impact assessments and change control for system upgrades, patches, and enhancements.
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Ensure alignment of CSV deliverables with GAMP 5, 21 CFR Part 11, Annex 11, and other applicable regulations.
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Collaborate with IT and Engineering teams for system integration (e.g., LIMS, ERP/SAP, DeltaV, PI Historian).
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Provide audit support during regulatory inspections (FDA, EMA, MHRA, etc.) and customer audits.
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Mentor junior validation engineers and support knowledge transfer on CSV best practices.
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Contribute to continuous improvement of MES validation strategies, procedures, and templates.
Qualifications
Qualifications
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Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field. Advanced degree preferred.
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7–10+ years of experience in Computer System Validation within GMP-regulated biologics/pharmaceutical manufacturing.
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Hands-on expertise with MES Syncade validation and configuration (recipes, workflows, batch records).
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Strong knowledge of regulatory guidelines: FDA 21 CFR Part 11, EU Annex 11, ICH Q7, GAMP 5.
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Experience in biologics manufacturing processes (cell culture, purification, fill/finish).
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Familiarity with integration points (DCS/DeltaV, LIMS, ERP/SAP, data historians).
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Excellent technical writing and documentation skills.
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Strong communication, leadership, and problem-solving abilities.
Preferred Skills
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Experience in large-scale biotech/biologics start-up or tech transfer projects.
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Knowledge of data integrity principles and ALCOA+ requirements.
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Exposure to quality management systems (TrackWise, Veeva, ValGenesis, Kneat).
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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.
