Summary
✨ AI‑Generated
An experienced validation engineering role focused on computerized systems in regulated manufacturing environments. Responsibilities include validation activities, automation system support, documentation, and collaboration with technical teams.
Highlights
Long-term consulting opportunity supporting critical pharmaceutical manufacturing systems with cross-functional engineering teams.
Description
CSV Engineer – DeltaV & Syncade
Location: New Hampshire
Work Model: On-site
Industry: Pharmaceutical / Biotechnology
Duration: Long-term project
About EFOR
EFOR is an international Life Sciences consulting group supporting pharmaceutical and biotechnology companies across Engineering, CQV, CSV, Automation, Quality, and Digital Transformation projects.
We partner with leading Life Sciences organizations across the U.S.
and internationally, providing technical expertise directly within client project teams.
Position Overview
EFOR is looking for an experienced CSV Engineer / CSV Lead with strong DeltaV and Syncade experience to support a pharmaceutical manufacturing project in New Hampshire.
The consultant will work on-site with Automation, Engineering, Quality, Manufacturing, IT/OT, and system integrators.
DeltaV experience is mandatory.
Key Responsibilities
Lead CSV activities for GMP automation and manufacturing systems.Support validation of Emerson DeltaV and Syncade.Develop and review:URSRisk AssessmentsValidation PlansTraceability MatricesIQ / OQ / PQ protocolsTest scriptsValidation Summary ReportsSupport testing of DeltaV control strategies, recipes, batch functionality, alarms, security, and audit trails.Support validation of Syncade workflows and Electronic Batch Records.Review DeltaV / Syncade integrations and other manufacturing-system interfaces.Participate in FAT, SAT, commissioning, and qualification activities.Manage deviations, change controls, and validation issues.Review and challenge vendor and system-integrator documentation.Ensure compliance with GAMP 5, 21 CFR Part 11, EU Annex 11, CSA, and GMP requirements.
Required Experience
Strong pharmaceutical / biotech CSV experience.Hands-on DeltaV experience — mandatory.Experience with Emerson Syncade / MES.Strong understanding of GMP automation systems.Knowledge of GAMP 5, CSA, 21 CFR Part 11, and data integrity.Experience with IQ / OQ / PQ and risk-based validation.Strong communication and critical-thinking skills.Ability to work on-site in New Hampshire.
Preferred Experience
DeltaV Batch.Syncade Electronic Batch Records.DeltaV / Syncade integrations.ISA-88.Commissioning & Qualification.Biotech or pharmaceutical manufacturing projects.
Ideal Profile
We are looking for someone who combines CSV expertise with strong technical knowledge of DeltaV and Syncade, and who can work effectively with Automation, Quality, Engineering, and Manufacturing teams.
Key requirement: CSV + DeltaV + Syncade + GMP experience.
