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Entry-Level Environmental Engineer / Scientist / Geologist
Loureiro Engineering Associates, Inc.
Plainville, CT
- $67,000 to $75,000 USD / year
Loureiro Engineering Associates is seeking an Entry-Level Environmental Engineer, Scientist, or Geologist to join our team in our Plainville, CT office.
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Full Stack Software Engineer
Globus Medical Inc
Audubon, PA
The Full Stack Software Engineer will be responsible for designing, developing, and maintaining both frontend and backend software for our Robotics products. This role spans modern web…
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Software Engineer
Stanley Martin Homes, LLC
Reston, VA
- $111,800 to $125,300 USD / year
As a key member of the Information Technology team, the Software Engineer will contribute to the development and maintenance of our cloud-hosted web applications, supporting internal and…
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Senior Data Technical Product Manager - Quantitative Sports
Hard Rock Digital
Remote, United States
Proven ability to write technical Jira tickets that translate a business need into work an engineer can pick up and deliver
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Group Manager - Land Development
LJA 2025
Myrtle Beach, SC
Provide technical advice and serve as the subject matter expert.
Added 1 min ago
Sr MS Engineer
General Datatech, LP
Dallas, TX
GDT Managed Services is hiring a Senior Linux Automation Engineer to own and expand the Linux operations and automation practice for our enterprise managed services customers. You will…
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BI Engineer
Health Care Service Corp.
Chicago, IL · Richardson, TX
…Marts and BI Semantic Data layer(s). This role required strong technical skills in platforms such as RDMBS, MPP Platforms (Teradata), Hadoop Datalake and Azure cloud with ability to design…
Added 1 min ago
Software Engineer - Salesforce Sales/Health Cloud
Humana Inc.
Louisville, KY · Atlanta, GA · Boston, MA · Charlotte, NC · Chicago, IL · Dallas, TX · Fort Lauderdale, FL · Nashville, TN · New York, NY · Tampa, FL · Washington, DC
Humana is seeking a Software Engineer 2 to help develop and support Salesforce Health Cloud solutions that power our growing Primary Care business. In this role, you will contribute to…
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Quality Engineer I
Resonetics
Dayton, OH
We are looking for a Quality Engineer I to join our growing team in Kettering, OH. This role applies Quality Engineering and scientific method techniques and principles to daily tasks and…
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Principal Systems Engineer
KBR
Chantilly, VA
- $157,000 to $235,000 USD / year
KBR is seeking a Principal Systems Engineer efforts for an Intelligence Community Space customer.
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Senior Systems Engineer
KBR
Beavercreek, OH
Bachelor’s or master's degree in engineering or related technical field.
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Senior Embedded Software Engineer (Top Secret Clearance)
STR
Woburn, MA
SDD is seeking a Senior Embedded Software Engineer to support the design, development, and implementation of real-time processing solutions in software for advanced multi-function Radar…
Added 1 min ago
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PRN Stationary Engineer
Aerotek
ROCKVILLE, MD
- $40 to $42 USD / hour
Job Title: Part Time Stationary Engineer Job DescriptionThis role provides critical support to hospital operations by maintaining, troubleshooting, and repairing building systems and…
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Facilities Mechanic
Aerotek
Silver Spring, MD
- $25 to $28 USD / hour
Background as a maintenance technician or building engineer supporting large, complex facilities.
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Staff DevSecOps Engineer
Legion Intelligence
Remote, United States
We’re looking for a Staff DevSecOps Engineer who will set technical direction across Platform DevOps and customer delivery. You will shape the engineering systems and practices that take…
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SO
Structural Staff Engineer
Salas O'Brien
Oakland, CA · San Diego, CA
- $90,000 to $105,000 USD / year
Our technical expertise is paired with an exceptional team of business development, human resources, finance and accounting, information technology, and marketing professionals, all of whom…
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SO
Structural Project Engineer
Salas O'Brien
HI
- $105,000 to $140,000 USD / year
Our technical expertise is paired with an exceptional team of business development, human resources, finance and accounting, information technology, and marketing professionals, all of whom…
Added 2 mins ago
Network Engineer III (ISP Focus)
EPB
Chattanooga, TN
The Network Engineer III is responsible for designing, configuring, and troubleshooting the data, video, and voice network. This role must provide complex, high-level technical support for…
Added 3 mins ago
Senior Power Electronics Engineer
Space Kinetic
El Segundo, CA
As a Senior Power Electronics Engineer, you will own the design, development, integration, and testing of power electronics and electrical power systems for Space Kinetic's payload and…
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Senior Motor and Power Controls Engineer
Space Kinetic
El Segundo, CA
As a Senior Power Electronics Engineer, you will own the design, development, integration, and testing of power electronics and electrical power systems for Space Kinetic's payload and…
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Electrical Design Engineer
Space Kinetic
El Segundo, CA · Albuquerque, NM
The Electrical Design Engineer will play a critical role in designing, building, and maturing prototypes for Space Kinetic’s core technology. You will support the team in refining the…
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Cloud Systems Engineer
FIRSTLIGHT
Albany, NY · Somerville, MA · Victor, NY · Town of Rockingham, VT · Brunswick, ME · Portsmouth, NH · Manchester, NH
…team that emphasizes knowledge sharing, skill development, and technical…
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Land Development Team Lead, Senior Project Manager
VHB
Charlotte, NC
- $150,000 to $180,000 USD / year
Have a direct impact on team culture, technical standards, and junior staff development
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ENGINEERING SOURCER
Platform Aerospace
Hollywood, MD · Blackstone, VA
As we continue to grow, we are seeking an experienced Engineering Sourcer to help identify and engage top technical talent supporting our engineering department. This role is ideal for…
Added 5 mins ago
Fast Track Summer Intern
Domtar Products
Ashdown, AR
Technical exposure to various production and support units within the electrical and mechanical teams supporting piping and instrumentation-based projects.

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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