0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant

Two River Consulting Partners; Summit (NJ); Hybrid; USD 80,000 - 100,000; Full time

Job summary

Two River Consulting Partners is seeking an experienced CSV Engineer in Summit, NJ. This role involves supporting the implementation and validation of ELLA and Synergy Neo2 laboratory instruments, with significant hands-on experience required in GxP compliant environments.

The ideal candidate must effectively manage multiple validation activities and communicate with various stakeholders. A hybrid work setup is available, with at least 50% on-site presence required.

Qualifications

• Strong CSV experience in a GxP laboratory or regulated life sciences environment.
• Experience with ELLA and Synergy Neo2 strongly preferred.
• Ability to manage multiple validation activities concurrently.

Responsibilities

• Support CSV activities for laboratory instrument implementation.
• Develop and review validation deliverables.
• Manage validation workstreams for multiple instruments.

Skills

CSV experience in GxP laboratory

Laboratory instrument implementation

Strong communication skills

Cross-functional teamwork

Job description

0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant

Please contact Amanda Mazza: [e-mail]

Job Overview

We are seeking an experienced CSV Engineer to support the implementation and validation of ELLA and Synergy Neo2 laboratory instruments. The ideal candidate should have hands‑on experience supporting GxP laboratory instrument implementations and be comfortable managing validation activities for both technologies in parallel.

Validation Engineer Responsibilities

• Support CSV activities for ELLA and Synergy Neo2 instrument implementation
• Develop, review, and/or execute validation deliverables including validation plans, risk assessments, test protocols, traceability matrices, summary reports, and related documentation
• Partner with laboratory, Quality, IT, and project stakeholders to ensure validation activities are completed on schedule
• Support GxP compliance, data integrity, and 21 CFR Part 11 considerations as applicable
• Manage validation workstreams for both instruments simultaneously
• Identify and escalate risks, gaps, delays, or documentation issues
• Support deviation resolution and documentation updates during protocol execution

Job Requirements

• Strong CSV experience in a GxP laboratory or regulated life sciences environment
• Prior experience with laboratory instrument implementation and validation
• Experience with ELLA and Synergy Neo2 strongly preferred
• Ability to manage multiple validation activities or technologies concurrently
• Familiarity with IQ/OQ/PQ, CSV lifecycle documentation, risk‑based validation, data integrity, and Part 11 expectations
• Strong communication skills and ability to work effectively with cross‑functional teams
• Experience supporting ECQ or lab equipment qualification
• Experience in biotech, pharma, plasma, or manufacturing laboratory environments
• Prior experience working in client‑facing hybrid/onsite roles

This role can be a local/hybrid setup. At minimum, a 50% on‑site presence is required.

LOCATION

50% onsite in Summit, NJ

EMPLOYMENT

Competitive C2C or W2 Contractor