Jobs in the United States

25+ jobs

Save this search

Added just now
Digital Platforms Engineer
Central Ohio Transit Authority
Columbus, OH
…minimum of five (5) years' professional experience as a Software Engineer, DevOps Engineer, or Systems Administrator. An equivalent combination of education and relevant experience will…
Added 5 mins ago
Project Engineer II
Pavion
Chantilly, VA
As a global leader, Pavion specializes in the design, installation, service, and maintenance of cutting-edge fire alarm systems, critical communications, video surveillance, access control,…
Added 5 mins ago
Applied AI Engineer
Axiomatic_AI
Boston, MA · Axiomatic_AI Middlesex County Cambridge, MA
Axiomatic AI is building a new class of AI systems designed to reason with the rigor of the scientific method. By combining deep learning with formal logic and physics-based modeling, we…
Added 6 mins ago
Cyber Security Engineer Senior
Amerihealth Caritas
United States
We are seeking a Cyber Security Engineer Senior for our Information Assurance team. The Cyber Security Engineer Senior will lead the vulnerability management program, own the RAMP process…
Added 7 mins ago
S
Cyber Security Engineer SME
SOSi
Washington, DC
- $119,803 to $248,822 USD / year
…government solutions business specializing in advanced technology systems and mission support. Its capabilities include data science, software development, network engineering,…
Added 7 mins ago
Principal Engineer, MEP & Building Systems
Anduril Industries
Costa Mesa, CA
We are looking for a Principal Engineer – MEP & Building Systems to join our rapidly growing team. This position sits within the broader Design & Construction (D&C) team and reports to the…
Added 7 mins ago
Mechanical Engineer, Space Special Programs
Anduril Industries
Chantilly, VA
Anduril Industries is a defense technology company with a mission to transform U.S. and allied military capabilities with advanced technology. By bringing the expertise, technology, and…
Added 8 mins ago
Forward Deployed Engineer
Morgan & Morgan, P.A.
United States
…consumer rights. Our over 6,000 employees are all united by one mission: For the…
Added 8 mins ago
Real-Time C/C++ Software Engineer
MIT Lincoln Laboratory
Lexington, MA
…that may range from rapid, high-risk efforts to longer-term mission programs. Your work will include multiple activities such as hardware and software development, systems analysis, data…
Added 9 mins ago
Principal Cyber Security Engineer
MANTECH
Chantilly, VA
MANTECH seeks a motivated, career and customer-oriented Principal Cyber Security Engineer to join our team in Chantilly, VA.
Added 9 mins ago
Principal Cyber Security Engineer
MANTECH
Chantilly, VA
MANTECH seeks a motivated, career and customer-oriented Principal Cyber Security Engineer to join our team in Chantilly, VA.
Added 9 mins ago
Welder
Kanthal Thermal Process Inc
United States
We are a company with a big heart and a mission to reduce climate impact through smarter industrial solutions. We offer a welcoming, inclusive environment, market-leading products, and…
Added 12 mins ago
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…
Added 13 mins ago
SM
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 14 mins 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 14 mins ago
K
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.
Added 14 mins ago
Senior Systems Engineer
KBR
Beavercreek, OH
Trinzic is the future independent company to be created through the planned spin-off of KBR's Mission Technology Solutions business, expected in January 2027. Our people work at the…
Added 14 mins ago
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…
Added 17 mins ago
ENGINEERING SOURCER
Platform Aerospace
Hollywood, MD · Blackstone, VA
Familiarity with engineering disciplines such as avionics, mechanical design, flight controls, mission systems, RF communications, SATCOM, autonomy, robotics, flight test, systems…
Added 18 mins ago
Senior AI Engineer
AJAIA
Remote, United States
As a Senior AI Engineer at Ajaia, you will lead the technical build of AI systems across client engagements and internal products where speed, adaptability, and execution quality matter.
Added 18 mins ago
Junior AI Engineer
AJAIA
Remote, United States
…operational value. From executive roadmapping to production-ready systems and workforce upskilling, Ajaia embeds intelligent tools directly into the workflows that matter…
Added 18 mins ago
AI Engineer
AJAIA
Remote, United States
…operational value. From executive roadmapping to production-ready systems and workforce upskilling, Ajaia embeds intelligent tools directly into the workflows that matter…
Added 19 mins ago
SC
Systems Engineer III - Design
SmartTech Contracting LLC
Remote, United States
- $78,750 to $95,812.5 USD / year
The Systems Engineer III - Design provides technical support to plan, schedule and execute design document deliverables for building automation system (BAS), electrical power monitoring…
Added 21 mins ago
Security Engineer - Networking
Shamrock Trading Corporation
Overland Park, KS
Shamrock’s mission since the start has been to create value and success for our customers, our partners and our people. Strong ethics, dedication to our customers and close attention to the…
Added 22 mins ago
Sr. Process Engineer, R1 Body AI/ML
Rivian
Normal, IL

PM Group

CSV Engineer II

Indianapolis, IN, United States

Apply About employer

Applications open in a new tab.

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

Apply About employer

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

Report this job