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PM Group

CSV Engineer II

Indianapolis, IN, United States

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Job details

Experience: 3-5 years of experience in computer system validation, laboratory systems, quality control, IT, automation, or pharmaceutical manufacturing support.
Posting language: English
Posted: Nov 9, 2026

Original job description

Overview

The CSV Engineer II position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services(OTS) team near Indianapolis, IN. Outsourced Technical Services (OTS) is an integral part of PM Group’s ability to support clients across the complete project life cycle. We have over 50 years’ industry experience, strong technical knowledge and integrated resources. Clients look to us to provide experienced technical professionals that complement their project teams. Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US.

We are looking for a CSV Computer System Validation Engineer II who will support protocol execution for laboratory computer systems within a GxP manufacturing site. This individual should have a foundational understanding of computer system validation principles and a strong desire to develop hands-on experience executing validation protocols for systems used in quality control, analytical testing, sample management, and laboratory data handling. The CSV Engineer will work under the guidance of senior CSV team members to execute and document validation activities, support deviation resolution, verify system functionality against approved requirements, and ensure testing evidence is complete, accurate, and inspection-ready. Project work will focus on regulated laboratory systems and related interfaces, including protocol execution, test script completion, discrepancy documentation, and adherence to site procedures, data integrity expectations, 21 CFR Part 11, EU Annex 11, GAMP 5, and applicable GMP requirements.

PM Group is an employee owned, international project delivery firm with a team of 4,000+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners.

Responsibilities

Execute approved CSV protocols and test scripts for laboratory computer systems in accordance with site procedures, project schedules, and GxP requirements.
Support validation activities for laboratory systems such as LIMS, CDS, ELN, SDMS, standalone instruments, instrument workstations, and related data acquisition or reporting applications.
Document test results clearly and accurately, including objective evidence, screenshots, printouts, attachments, and traceability to approved requirements.
Identify, document, and escalate protocol discrepancies, test failures, and deviations in accordance with site quality procedures.
Perform verification of user access, audit trails, electronic records, electronic signatures, data integrity controls, backup/restore, and other applicable Part 11 and Annex 11 requirements.
Assist with preparation and review of validation deliverables, including test protocols, requirements traceability matrices, summary reports, and supporting attachments.
Coordinate with laboratory operations, Quality, IT, Automation, vendors, and senior CSV resources to schedule and complete testing without disrupting manufacturing or laboratory operations.
Maintain compliance with PM Group’s Service Delivery Platforms, Quality Management System, client procedures, and applicable GMP expectations.

Qualifications

Bachelor’s degree in Engineering, Computer Science, Life Sciences, Information Systems, or a related technical discipline.
3-5 years of experience in computer system validation, laboratory systems, quality control, IT, automation, or pharmaceutical manufacturing support.
Foundational knowledge of GxP, GMP documentation practices, data integrity, and computer system validation lifecycle principles.
Familiarity with 21 CFR Part 11, EU Annex 11, GAMP 5, and risk-based validation concepts is preferred.
Experience executing test scripts, documenting evidence, managing discrepancies, or supporting validation documentation is preferred.
Exposure to laboratory systems such as LIMS, CDS, ELN, SDMS, analytical instruments, or instrument control software is a plus.
Strong attention to detail, technical writing ability, and commitment to producing clear, complete, and inspection-defensible documentation.
Ability to work collaboratively with laboratory personnel, Quality, IT, vendors, and project team members in a regulated manufacturing environment.
Proficiency with Microsoft Word, Excel, and standard documentation tools.
Ability to travel as needed for client and project support.

All of your information is confidential according to EEO guidelines. Why PM Group? As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2026 business strategy. Click here to read more in our 2025 Environmental, Social and Governance Report.

Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.

PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

RECRUITMENT AGENCIES NEED NOT APPLY

Execute approved CSV protocols and test scripts for laboratory computer systems in accordance with site procedures, project schedules, and GxP requirements.
Support validation activities for laboratory systems such as LIMS, CDS, ELN, SDMS, standalone instruments, instrument workstations, and related data acquisition or reporting applications.
Document test results clearly and accurately, including objective evidence, screenshots, printouts, attachments, and traceability to approved requirements.
Identify, document, and escalate protocol discrepancies, test failures, and deviations in accordance with site quality procedures.
Perform verification of user access, audit trails, electronic records, electronic signatures, data integrity controls, backup/restore, and other applicable Part 11 and Annex 11 requirements.
Assist with preparation and review of validation deliverables, including test protocols, requirements traceability matrices, summary reports, and supporting attachments.
Coordinate with laboratory operations, Quality, IT, Automation, vendors, and senior CSV resources to schedule and complete testing without disrupting manufacturing or laboratory operations.
Maintain compliance with PM Group’s Service Delivery Platforms, Quality Management System, client procedures, and applicable GMP expectations.
Bachelor’s degree in Engineering, Computer Science, Life Sciences, Information Systems, or a related technical discipline.
3-5 years of experience in computer system validation, laboratory systems, quality control, IT, automation, or pharmaceutical manufacturing support.
Foundational knowledge of GxP, GMP documentation practices, data integrity, and computer system validation lifecycle principles.
Familiarity with 21 CFR Part 11, EU Annex 11, GAMP 5, and risk-based validation concepts is preferred.
Experience executing test scripts, documenting evidence, managing discrepancies, or supporting validation documentation is preferred.
Exposure to laboratory systems such as LIMS, CDS, ELN, SDMS, analytical instruments, or instrument control software is a plus.
Strong attention to detail, technical writing ability, and commitment to producing clear, complete, and inspection-defensible documentation.
Ability to work collaboratively with laboratory personnel, Quality, IT, vendors, and project team members in a regulated manufacturing environment.
Proficiency with Microsoft Word, Excel, and standard documentation tools.
Ability to travel as needed for client and project support.

RECRUITMENT AGENCIES NEED NOT APPLY

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More about this job

Skills

Inspection
Documentation
Good manufacturing practices
LIMS
Reporting
Regulatory compliance
Quality assurance procedures
Computer science
Quality control
Pharmaceutical processes
Attention to detail
Technical writing
Microsoft Word
Microsoft Excel
Recruitment

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