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CSV Engineer

Job in Portsmouth, Rockingham County, New Hampshire, 00215, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Quality Engineering, Systems Engineer, Electrical Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: CSV  Engineer

CSV Engineer – Katalyst CRO

Join to apply for the CSV Engineer role at Katalyst CRO.

This position is open for applicants to be among the first 25 candidates.

Job Description

The CSV Engineer will serve as an individual contributor responsible for ensuring compliance with industry regulations and standards while driving efficiency in site and process improvement projects. This role requires expertise in computer system validation, controls automation, and GMP documentation, with a focus on Delta

V and Syncade MES systems. The engineer will collaborate with the CSV team to identify roadblocks, assess risks, and implement best practices across critical systems.

Responsibilities
  • Act as CSV owner for major site and process improvement projects.
  • Conduct risk assessments of systems and processes.
  • Review change requests, test scripts, and draft validation protocols.
  • Initiate and review GMP documentation revisions.
  • Execute QMS processes including Change Control (Delta

    V, Syncade MES), Deviations, and CAPAs.
  • Collaborate with cross‑functional teams to ensure compliance with regulatory requirements and industry standards.
  • Provide input during project scoping to identify efficiencies and potential roadblocks.
Requirements
  • Bachelor's degree in engineering, Computer Science, Life Sciences, or related field.
  • Advanced degree (Master's) preferred but not mandatory.
  • Additional certifications in CSV, GMP, or Quality Systems are a plus.
  • Substantial hands‑on experience in equipment and/or computer system validations.
  • Strong working knowledge of Controls Automation, Process Control Systems, Distributed Systems, and MES (Delta

    V preferred).
  • Prior experience leading projects in Biotech, Pharma, or biologics industries.
  • Proven ability to work independently, with strong attention to detail and ability to meet deadlines.
Seniority level

Associate

Employment type

Contract

Job function

Pharmaceutical Manufacturing

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