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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…
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…
Added 1 min ago
Software Engineer
KBR
Beavercreek, OH
KBR is seeking a highly motivated and experienced Software Engineer to be a part of the team that supports the Department of the Air Force’s advanced air platform testing and rapid…
Added 1 min ago
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…
Added 1 min ago
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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.
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 2 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…
Added 2 mins ago
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…
Added 4 mins ago
Fast Track Summer Intern
Domtar Products
Ashdown, AR
Designing and estimating small projects under the supervision of a staff engineer or engineering manager.
Added 5 mins ago
Town Engineer
Chapin
Chapin, SC
The Town of Chapin is seeking a licensed Professional Engineer to serve as Town Engineer for the Utilities Department. This position is the Town’s primary technical lead for water…
Added 5 mins ago
Manufacturing Engineer
LSI Industries, Inc.
Houston, TX
Proficiency in Microsoft Excel and working knowledge of Microsoft Office applications.
Added 6 mins ago
Junior AI Engineer
AJAIA
Remote, United States
As a Junior AI Engineer at Ajaia, you will build and ship AI-enabled software across client engagements and internal products, working alongside senior engineers who will review your work…
Added 6 mins ago
Water Resources - Project Manager
Civil & Environmental Consultants, Inc.
Knoxville, TN
As a Water Resource Engineer for Civil & Environmental Consultants, Inc. (CEC) in our Knoxville, TN office, you’ll work collaboratively within an employee-owned firm while supporting…
Added 7 mins ago
IG
Software Engineer
Insight Global
Overland Park, KS
- From $40 USD / hour
Strong software engineering fundamentals with experience supporting legacy applications.
Added 9 mins ago
Web Developer
CACI
Chantilly, VA · Chantilly
CACI is seeking a Web Developer to help modernize and enhance a portfolio of 100+ web applications supporting a government customer. You’ll solve technical challenges across the development…
Added 9 mins ago
Senior Mechanical Engineer
Twenty-Six Defense
Merrimack, NH
…wide range of programs for innovative defense and commercial…
Added 9 mins ago
Sr. Process Engineer, R1 Body AI/ML
Rivian
Normal, IL
Added 9 mins ago
CSV Engineer II
PM Group
Indianapolis, IN
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)…
Added 9 mins ago
Web Developer
CACI, INC.-FEDERAL
Chantilly, VA
CACI is seeking a Web Developer to help modernize and enhance a portfolio of 100+ web applications supporting a government customer. You’ll solve technical challenges across the development…
Added 10 mins ago
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Sr. AI/ML Engineer - Remote
UnitedHealth Group
Richardson, TX
- $120,100 to $214,500 USD / year
The Optum Health Technology team is seeking a Senior AI/ML Engineer with a solid data science background to build and scale cutting-edge AI-powered solutions that transform value-based care…
Added 10 mins ago
Designer - Substation
Quanta Infrastructure Solutions Group, LLC
Baton Rouge, LA
…use in-house talent, expertise and resources to plan, design, engineer, manage, conduct maintenance on and construct…
Added 10 mins ago
Test Engineer II
Thorlabs
Newton, NJ
…assist compliance by designing and testing set-ups for approval applications; recording test results; preparing investigative reports; preparing and filing Declarations of Conformity;…
Added 11 mins ago
Thermal Sciences Senior Associate (Ph.D.)
Exponent Inc.
Natick, MA
…transfer, mass transport, combustion and electrochemistry. Applications will primarily be in vehicles, consumer electronics, utilities, fire and explosion investigation, power generation,…
Added 11 mins ago
O
Site Reliability Engineer 2
Oracle
Nashville, TN
- $69,800 to $148,300 USD / year
As a Site Reliability Engineer, you will apply software engineering, systems engineering and networking practices to improve the reliability, availability, performance, and scalability of…

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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