Jobs in the United States

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Added 2 hours ago
Supplier Eng - P3
Boston Scientific
United States
This role follows an on-site position work model requiring employees to be in our local Dorado office four (4-5) days per week
Added 2 hours ago
Project Support Specialist Security Engineer III
Deloitte US
Tampa, FL
As a Project Support Specialist Security Engineer III on the Project team, you will be responsible for…
Added 2 hours ago
WI
(USA) Network Engineer III
Walmart Inc.
United States
- $80,000 to $155,000 USD / year
…deployment meets operational and business objectives before project completion, supporting seamless network functionality and…
Added 2 hours ago
MK1 EPS Test Engineer III
Blue Origin Personnel, LLC
United States
As an EPS Test Engineer on the Lunar Core Components team, you will serve as the test engineer for one or more Electrical Power System (EPS) Products across the MK1 Lunar Lander Vehicle.…
Added 3 hours ago
Field Engineer III - Mechanical
Worley
Baytown, TX · Baytown
…high-quality construction execution. As a Mechanical Field Engineer III, you will work directly at the project site to interpret design requirements, evaluate field conditions, resolve…
Added 3 hours ago
TA
Civil Engineer - III/IV
TOTH AND ASSOCIATES INC
Springfield, MO · Kansas City, MO
- $90,000 to $140,000 USD / year
EIT certification required
Added 4 hours ago
Software Engineer III, Infrastructure, Google Cloud Networking
Google
Sunnyvale, CA
…mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google’s needs with opportunities to switch teams and projects as…
Added 4 hours ago
Software Engineer III, Security/Privacy, Google Cloud Security and Privacy
Google
Kirkland, WA
…mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google’s needs with opportunities to switch teams and projects as…
Added 4 hours ago
Principal Statistician
MED Medtronic Inc
Minneapolis, MN
…growth and cross-functional collaboration as we work together to engineer the…
Added 4 hours ago
EM
EMI/EMC Technician III
Element Materials Technology
Rockford, IL
- $25.39 to $42.33 USD / hour
Requires very little supervision and technical input of a Department Manager, Principal Technician, Project Coordinator or Engineer
Added 5 hours ago
Research Engineer II / III
The J David Gladstone Institutes
United States
The Finkbeiner Lab at the Gladstone Institutes in San Francisco, CA is hiring a Research Engineer (level II or III, depending on experience) to develop, operate and maintain our custom and…
Added 5 hours ago
Oracle Data Integrator (ODI)/ETL Developer
Deloitte US
Washington, DC
As a Project Data Engineer III on the AI & Data team, you will support ODI development and data integration from multiple reporting sources to reporting systems and leverage the…
Added 5 hours ago
CADD Technician III
HNTB Corporation
Kansas City, MO
Are you ready to make a significant impact on fast-paced infrastructure projects? HNTB is looking for a CADD Technician III to join our Design Build Team.
Added 5 hours ago
Inspector III
HNTB Corporation
Madison, WI
…discipline/trade performed by the contractor in order to monitor the project compliance with plans, specifications and other contract provisions. Maintains daily logs of inspection work…
Added 5 hours ago
Construction Rep III
HNTB Corporation
Madison, WI
…and criteria to perform assignments and assist the Resident Engineer in partnership with the project team. This position maintains project data, including drawings and specifications,…
Added 5 hours ago
Field Engineer III
HNTB Corporation
Madison, WI
…Monitors contractor's construction progress as compared to overall project and contract schedule. Responsible for assisting in the compliance and modification of design calculations,…
Added 5 hours ago
Architect III
Zachry Group
Downers Grove, IL
Must possess permanent authorization to work in the USA without the need of sponsorship now or in the future · Must possess a vision (corrected or uncorrected) that allows for clear visibility from a distance of 20 inches or less
Added 5 hours ago
Mechanical Engineer III Energy Productio
MADISON GAS & ELECTRIC CO
MADISON, WI
Added 5 hours ago
Engineer III, Supplier Quality
ThermoFisher Scientific
Madison, WI
…global healthcare, research, and safety. As a Supplier Quality Engineer III, you'll ensure the quality and reliability of our supply chain while contributing to our mission of enabling…
Added 5 hours ago
Critical Environments Operator III
CyrusOne Management Services LLC
Quincy, WA
Provides coordination with contractors and vendors as needed for the effective and safe accomplishment of maintenance and project work.
Added 6 hours ago
Director of Engineering Programs
Yulista Services LLC
Huntsville, AL
Project Management Professional (PMP) certification or DAWIA Level III Program Management certification.
Added 6 hours ago
Sr Databricks Data Engineer
Deloitte US
Atlanta, GA · Austin, TX · Boston, MA · Charlotte, NC · Chicago, IL · Cincinnati, OH · Cleveland, OH · Columbus, OH · Costa Mesa, CA · Dallas, TX · Denver, CO · Detroit, MI · Houston, TX · Indianapolis, IN · Kansas City, MO · Los Angeles, CA · McLean, VA · Miami, FL · Minneapolis, MN · Morristown, NJ · Nashville, TN · NY · Philadelphia, PA · Pittsburgh, PA · Rosslyn, VA · Sacramento, CA · San Diego, CA · San Francisco, CA · San Jose, CA · Seattle, WA · Stamford, CT · Tampa, FL · Tempe, AZ
As a Data Engineer III on the AI & Data team, you will be responsible for:
Added 6 hours ago
Java Full Stack Developer-Software Engineer III
Deloitte US
San Francisco, CA · St. Louis, MO
…in a collaborative environment? As an experienced Software Engineer III- Sr. Java Full Stack Developer you will have the ability to share new ideas and collaborate on projects as a…
Added 6 hours ago
HC
R&D Software Quality Assurance Engineer III
Hach Company
Loveland, CO
- $115,000 to $120,000 USD / year
Growing your expertise and expanding your skillset with every project.
Added 6 hours ago
Engineer III, Quality-Manufacturing
ICU MEDICAL INC
SALT LAKE CITY, UT

PM Group

CQV Engineer III

Conshohocken, PA, United States

Apply on careers.pmgroup-global.com About employer

Applications open in a new tab.

Job details

Experience: 5-10 Years of CQV experience in the Pharmaceutical, Life Sciences, Biotech and/or Cell & Gene Therapy industries
Posting language: English
Posted: Nov 9, 2026

Original job description

Overview

The CQV Engineer III position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services(OTS) team in Indiana. 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.

This is a mid-level career position and we are looking for a professional who enjoys client interaction as well as the technical aspects of the position. This position requires an understanding of the technical aspects of commissioning (Cx), qualification and validation (CQV). The ability to successfully handle multiple real-time complex projects while maintaining a strong work ethic, and drive to deliver for clients, as a collaborative colleague, is necessary for this role. An understanding and applying the principals of good documentation practices (CGDP) is essential to performing in this position. The CQV Engineer III is mentored by more senior level CQV team members, provide guidance to less experienced CQV staff and will report to the Director of CQV. Their responsibilities will include document development as well as testing execution to meet client qualification needs. Expect project work to include all levels of qualification from design to completion. Must be willing to travel to the client site.

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

Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS)
Independently interact with client to asses and continuously reassess client needs
Perform quality GAP analysis
Author technical and scientific reports
Demonstrates an understanding of project scope of work assigned
Demonstrates an understanding of commercial aspects (hours and capital cost) of their work
Delivers scope of work within budgeted hours
Document development as well as testing execution to meet client qualification needs
Applying the principals of good documentation practices (CGDP)
Collaborate in a multi discipline team environment
Perform qualification protocols and review other team members qualification documents
Ensure the implementation of current good manufacturing practices (CGMP)
Independently assess the qualification needs of equipment, facilities, utilities and systems
Provide technical guidance to less experience CQV team members
Special projects as assigned

Qualifications

Bachelor’s degree is required; an engineering degree is preferred
5-10 Years of CQV experience in the Pharmaceutical, Life Sciences, Biotech and/or Cell & Gene Therapy industries
Factory site acceptance testing (FAT) and site acceptance testing (SAT) experience
Proven experience with commissioning pre-functional checklist (PFC) development and commissioning functional performance testing (FPT)
Experience working with current good engineering and current good manufacturing practices
Understand client needs and provide assistance with the development of user requirements specifications (URS) and system impact analysis (SIA)
Demonstrated experience working in an industry regulated life sciences environment
Actively participant in the document approval process
Understanding of the entire validation life cycle and change control process
Experience reviewing vendor supplied documents such as submittal sheets and turn over packages (TOPs)
Familiar with and understand the basics of design drawings
Full understanding of all commissioning, qualification and validation (CQV) testing procedures
Ability to document and execute cleaning validation procedures
Knowledge of cGMP Manufacturing environments is required
Good technical reporting writing skills are mandatory
The ability to travel as needed for client development and project execution

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

Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS)
Independently interact with client to asses and continuously reassess client needs
Perform quality GAP analysis
Author technical and scientific reports
Demonstrates an understanding of project scope of work assigned
Demonstrates an understanding of commercial aspects (hours and capital cost) of their work
Delivers scope of work within budgeted hours
Document development as well as testing execution to meet client qualification needs
Applying the principals of good documentation practices (CGDP)
Collaborate in a multi discipline team environment
Perform qualification protocols and review other team members qualification documents
Ensure the implementation of current good manufacturing practices (CGMP)
Independently assess the qualification needs of equipment, facilities, utilities and systems
Provide technical guidance to less experience CQV team members
Special projects as assigned
Bachelor’s degree is required; an engineering degree is preferred
5-10 Years of CQV experience in the Pharmaceutical, Life Sciences, Biotech and/or Cell & Gene Therapy industries
Factory site acceptance testing (FAT) and site acceptance testing (SAT) experience
Proven experience with commissioning pre-functional checklist (PFC) development and commissioning functional performance testing (FPT)
Experience working with current good engineering and current good manufacturing practices
Understand client needs and provide assistance with the development of user requirements specifications (URS) and system impact analysis (SIA)
Demonstrated experience working in an industry regulated life sciences environment
Actively participant in the document approval process
Understanding of the entire validation life cycle and change control process
Experience reviewing vendor supplied documents such as submittal sheets and turn over packages (TOPs)
Familiar with and understand the basics of design drawings
Full understanding of all commissioning, qualification and validation (CQV) testing procedures
Ability to document and execute cleaning validation procedures
Knowledge of cGMP Manufacturing environments is required
Good technical reporting writing skills are mandatory
The ability to travel as needed for client development and project execution

RECRUITMENT AGENCIES NEED NOT APPLY

Apply on careers.pmgroup-global.com About employer

More about this job

Skills

Regulatory compliance
Quality assurance procedures
Documentation
Good manufacturing practices
Design drawings
Cleaning
Reporting
Recruitment

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Work requirements

Jobs in the United States