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Laboratory Instrument Support Specialist Jobs (NOW HIRING)

Yoh,-A-Day-

Research Associate

Framingham, MA · On-site

$32/hr

Laboratory Systems & Instrument Support * Provide day‑to‑day operational support for computerized laboratory instruments, applications, and associated systems. * Monitor system performance and ...

Novo Nordisk A/S

Quality Control Instrument Area Specialist - DPM DU Location: Durham, NC, US About the Department ... The Position Works closely with Laboratory personnel to support repairs, preventive maintenance ...

PACIV

IT / CSV Specialist

San Juan, PR · On-site

Provide IT support for laboratory applications such as Empower, SmartLab, and Darwin LIMS ... Knowledge of laboratory instrument connectivity and LAC/E systems. * Experience with Veeva QMS ...

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Laboratory Instrument Support Specialist information

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How much do laboratory instrument support specialist jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for laboratory instrument support specialist in the United States is $30.21, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $37.50 per hour, depending on experience, location, and employer.

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

Summit, NJ • On-site

Two River Consulting Partners
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Re-posted 11 days ago

Job description

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

Please contact Amanda Mazza: amanda@tworivercp.com

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

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