Jobs in the United States

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Added 3 mins ago
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Senior Manufacturing Engineer
Actalent
Wilmington, MA
- $80 to $90 USD / hour
Develop and standardize assembly processes, control plans, maintenance strategies, and operational documentation that are appropriate for the maturity level of the product and process.
Added 3 mins ago
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Sterile Construction Project Manager
Actalent
King of Prussia, PA
- $65 to $95 USD / hour
…agreed-upon processes. The Project Manager manages four critical control processes: weekly schedule verification, cost and change control, the Request for Information (RFI) process with the…
Added 3 mins ago
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Controls Engineer
Actalent
Sterling, VA
- $39.42 to $50 USD / hour
Commission and validate automation/control systems
Added 3 mins ago
Senior Mold Design Engineer
BIOMERICS LLC
Winston-Salem, NC
The Senior Mold Design Engineer is the primary authority for mold design, tooling strategy, process selection, and molding technology. This individual defines tooling concepts, recommends…
Added 3 mins ago
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Controls Engineer (Expert)
Actalent
Shelbyville, IN
- $48.08 to $57.69 USD / hour
Job Title: Controls EngineerJob DescriptionThis Controls Engineer role focuses on designing, programming, and commissioning automated control systems within a high-volume automotive glass…
Added 3 mins ago
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Electrical Engineer
Actalent
Riverdale, IA
- $75,000 to $120,000 USD / year
Create and develop electrical control solutions that support process improvements, enhance equipment reliability, and increase overall operational efficiency.
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Embedded Software Engineer
Actalent
Kansas City, KS
- $41 to $51 USD / hour
Embedded Software EngineerJob DescriptionThe Embedded Software Validation Engineer validates, verifies, and tests embedded vehicle control software for both new and existing products. This…
Added 3 mins ago
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Cyber Security Engineer SME
SOSi
Washington, DC
- $119,803 to $248,822 USD / year
SOSI is seeking a Senior Cybersecurity Engineer to serve as a technical subject matter expert supporting an enterprise cyber defense program for a federal customer. This senior, highly…
Added 3 mins ago
Principal Engineer, MEP & Building Systems
Anduril Industries
Costa Mesa, CA
Provide technical direction on HVAC system selection, electrical distribution strategy, plumbing and process piping layouts, fire protection approaches, and building automation and controls…
Added 7 mins ago
Staff Data Scientist
John Deere
IL · Deer Creek
…technology suite, including its machines, precision technologies, automation and autonomy features, and digital…
Added 9 mins ago
Automation & Controls Engineer (Mandarin)
Smithfield
Sioux Falls, SD
Are you passionate about cutting-edge technology and driving innovation in automation? As an Automation and Controls Engineer, you’ll be at the heart of revolutionizing our facility’s…
Added 13 mins ago
Maintenance Performance Engineer - Warehouse Automation & Robotics
Exotec
Atlanta, GA
Exotec designs and delivers advanced automation solutions that help global brands optimize warehouse performance while supporting warehouse teams across every level. Our organization…
Added 13 mins ago
Software Integration Engineer - Automation & Robotics
Exotec
Atlanta, GA
Exposure to warehouse management systems (WMS), warehouse control systems (WCS), warehouse execution systems (WES), logistics, fulfillment, industrial automation, robotics, or material…
Added 13 mins ago
Integrator Performance Engineer - Warehouse Robotics Automation
Exotec
Atlanta, GA
Solve issues escalated from Exotec Control Center and integrator
Added 15 mins ago
Senior AI Engineer
AJAIA
Remote, United States
…core pillars: AI Strategy and Advisory, AI Engineering and Automation, Workforce Training and Enablement, and Custom Product…
Added 16 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 18 mins ago
PG
CQV Engineer I
PM Group
Rahway, NJ
- $75,000 to $90,000 USD / year
0-3 years of experience in computer system validation, laboratory systems, quality control, IT, automation, or pharmaceutical manufacturing support.
Added 18 mins ago
CSV Engineer II
PM Group
Indianapolis, IN
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…
Added 32 mins ago
UF
Automation Engineer
United Flow Technologies
DeKalb County, GA
- $92,000 to $135,000 USD / year
The Automation Engineer is the core technical role in Tesco’s future engineering organization. Rather than separating electrical panel designers, PLC programmers, SCADA engineers, and…
Added 35 mins ago
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Electrical Engineer
Actalent
Deer Park, NY
- $100,000 to $125,000 USD / year
An industry-leading manufacturer of highly specialized industrial equipment is seeking an experienced Electrical Engineer to join its engineering team in Deer Park, NY. This organization is…
Added 35 mins ago
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Mechanical Design Engineer
Actalent
Amsterdam, NY
- $36.06 to $38.46 USD / hour
We are seeking a Mechanical Design Engineer to join a growing engineering team supporting critical power generation equipment used in industrial, utility, and power plant environments. This…
Added 35 mins ago
Release Manager
eVisit
Remote, United States
…production across every Delivery Team. You are air traffic control for each release: you know what is in it and what is not, you coordinate the teams contributing to it, you own the…
Added 41 mins ago
Software Engineer [Multiple Positions Available]
JPMC page
Tampa, FL
…proxy balancer modules for dynamic load balancing; utilizing automation and management of load balancers for high availability architectures, including Local Traffic Managers (LTM) and…
Added 44 mins ago
Cyber Security Engineer
BRMi
UNAVAILABLE, VA · MD · FL · TX · DC
We are seeking an experienced Cybersecurity Engineer to support enterprise application whitelisting, application control, and daily endpoint security operations. This role focuses on…
Added 51 mins ago
SD
Composite Machining Manufacturing Engineer
SST Direct
North Austin, TX
- $95,000 to $125,000 USD / year
DIRECT HIRE: The Composite Machining Manufacturing Engineer develops, implements, and improves machining processes for advanced aerospace composite structures. This role supports…

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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