Katalyst CRO
CSV Engineer – Katalyst CRO
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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 DeltaV 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 (DeltaV, 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 (DeltaV 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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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 DeltaV 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 (DeltaV, 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 (DeltaV 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
#J-18808-Ljbffr