Lonza

pharmaceutical

SeniorValidationEngineer-CSV(OT)

$93–93k Vacaville, California, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Validation Engineer - CSV (OT) at Lonza. Skills: Validation, cGMP, Process Automation Systems, Computerized Systems. Lead and execute validation activities. Ensure compliance with regulatory requirements”

What You'll Achieve.

Ensure compliance with regulatory requirements and internal quality standards; Manufacture medicines to the highest quality and safety standards

Industry & Context.

pharmaceutical
Problems you'll solve

problem-solving ability

Eligibility Requirements

fully site‑based role

What They're Looking For.

Must Have

Bachelor's degree in Engineering (Computer Science, Information Technology), Life Sciences, a related field or significant related work experience, Minimum of 5-8 years of experience in validation within the pharmaceutical, biotechnology, or medical device industry, Extensive knowledge of cGMP, FDA, EMA, and other relevant regulatory requirements for validation activities, Proven experience with validation of the Process Automation Systems, Distributed Control System (DCS), Manufacturing Control System (MCS), Programmable Logic Controllers (PLC), Building Automation System (BAS) and manufacturing equipment/systems is required, Direct validation experience and/or GMP operations experience with increasing levels of responsibility for a wide range of validation projects including validation of large-scale biochemical manufacturing equipment, facilities, utility, automation and computerized systems

Nice to Have

Experience with server administration, NetApp storage technologies, core network infrastructure fundamentals

What You'll Do.

Lead and execute validation activities

Ensure compliance with regulatory requirements

Oversight and performance of Commissioning and Qualification

Leverage risk management principles

review and approve validation documents

and review validation protocols

Peer review/approve validation protocols

Monitor and track validation schedules

Provide technical leadership

Support internal and external audits

How You'll Work.

Team & Collaboration

Working together in person supports close, real‑time collaboration; Representing Engineering Validation on project teams; Coordinate activities of Engineering, MSAT, Manufacturing, Quality; Work independently and as part of a team

Communication Scope

verbal communication; technical explanations

Process & Methodology

Manage projects, Lead larger scale projects

Full Job Description

**Location:** Vacaville, California This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. **What you will get:** The full-time base annual salary for this position is expected to range between $93,000 to $155,000. In addition, below you will find a comprehensive summary of the benefits package we offer: * Performance-related bonus * Medical, dental and vision insurance * 401(k) matching plan * Life insurance, as well as short-term and long-term disability insurance * Employee assistance programs * Paid Time Off The Senior Validation Engineer (Computer System Validation) - Operational Technology, at Lonza will be responsible for leading and executing validation activities for manufacturing processes, equipment, computerized systems, and automation control systems to ensure compliance with regulatory requirements and internal quality standards. This role requires a strong understanding of cGMP principles and a proven track record in a pharmaceutical or biotechnology manufacturing environment. **What you will do:** * Responsible for oversight and performance of Commissioning and Qualification of computerized equipment, utility systems, facilities, automation control systems, and site computerized systems. * Leverage risk management principles to drive risk-based validation testing and decision-making. * Author, review and approve validation master plans, project plans, validation protocols, validation reports, deviations, and change controls in accordance with Lonza's quality management system. * Develop, execute, and review validation protocols (DQ, IQ, OQ, PQ) for new and modified equipment, processes, and systems. * Peer review/approve validation protocols, and summary reports generated by junior and contract personnel; monitor and track validation schedules and progress, escalating any potential delays or issues to m

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