Senior CSV Engineer – Project Lead jobs in United States
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Katalyst CRO · 3 weeks ago

Senior CSV Engineer – Project Lead

Katalyst CRO is a company focused on Computer System Validation, and they are seeking a Senior CSV Engineer – Project Lead to lead and execute validation activities for GxP-regulated systems. This role involves managing validation projects, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to support system implementations and improvements.

AnalyticsBiopharmaData ManagementHuman ResourcesQuality Assurance
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

Lead and manage end-to-end CSV activities for GxP-regulated systems, with primary ownership of EBR platforms
Plan, execute, and review validation deliverables including URS, FRS, risk assessments, IQ/OQ/PQ, and validation reports
Ensure compliance with FDA, GAMP 5, 21 CFR Part 11, and other global regulatory standards
Provide technical guidance and project leadership across multiple validation projects
Collaborate with Quality, IT, Manufacturing, Automation, and vendors during system implementations and upgrades
Support change management, deviation management, and periodic reviews for validated systems
Ensure validation activities are completed on schedule and within project scope
Drive continuous improvement initiatives to enhance validation processes and system compliance
Act as a key point of contact for audits and regulatory inspections related to CSV

Qualification

Computer System ValidationElectronic Batch RecordFDA regulationsGAMP 521 CFR Part 11Stakeholder managementProject managementDocumentation skillsCommunication skillsRegulatory audits experiencePharmaceutical industry experienceBiotech industry experienceLife sciences industry experienceCross-functional team leadership

Required

Strong experience in Computer System Validation (CSV) within GxP-regulated environments
Hands-on experience with Electronic Batch Record (EBR) systems
In-depth knowledge of FDA regulations, GAMP 5, and 21 CFR Part 11 compliance
Proven experience leading validation projects and cross-functional teams
Excellent documentation, communication, and stakeholder management skills
Ability to work effectively with internal teams and external vendors
Experience in pharmaceutical, biotech, or life sciences industries
Prior experience handling regulatory audits and inspections

Preferred

Project management experience or certification is an advantage

Company

Katalyst CRO

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Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide.

H1B Sponsorship

Katalyst CRO has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (37)
2024 (14)
2023 (24)
2022 (52)
2021 (54)
2020 (39)

Funding

Current Stage
Growth Stage

Leadership Team

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John Patil
Recruiter, Pharma/CRO Staffing Division
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Company data provided by crunchbase