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Job Title: Senior CQV Validation Engineer – Combination Products & Packaging Manufacturing - (JP15567)
Location: New Albany, OH. 43054
Employment Type: Contract
Business Unit: Site Process Development Group
Duration: 6+ months (with likely extensions and/or conversion to permanent)
Posting Date: 07/16/26
Pay Rate: $55 - $63/hour W2
Notes: Only qualified candidates need apply.
3 Key Consulting is hiring a Senior CQV Validation Engineer – Combination Products & Packaging Manufacturing for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Senior Validation Process Development Engineer serves as a technical leader responsible for supporting commercial GMP manufacturing operations while driving the development, characterization, optimization, and validation of automated and semi-automated combination product assembly and packaging processes. This role applies advanced engineering principles to ensure robust, compliant and efficient manufacturing processes that support both commercial production and new product introduction.
The engineer provides day-to-day technical support for commercial manufacturing through equipment and process troubleshooting, critical process parameter assessment and optimization, process performance monitoring, deviation investigations, root cause analysis, and implementation of continuous improvement initiatives to enhance product quality, process capability, and operational excellence.
Working cross-functionally with Manufacturing, Quality, Validation, Engineering and other technical organizations, the Senior Engineer leads complex engineering initiatives, resolves technical challenges, and identifies opportunities to improve equipment reliability, process performance, and manufacturing capability. This individual serves as a Subject Matter Expert (SME) for combination products, device assembly technologies, and GMP manufacturing processes, ensuring compliance with regulatory requirements while supporting the successful commercialization and lifecycle management of the business’s product portfolio.
Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:

• Demonstrated experience leading Commissioning, Qualification, and Validation (CQV) activities within a GMP-regulated biotechnology or pharmaceutical manufacturing environment, with direct experience supporting packaging equipment, combination products, and/or device assembly processes.
• Hands-on experience using electronic quality and document management systems, including KNEAT, Veeva, TrackWise, or equivalent platforms for managing validation documentation, change controls, deviations, CAPAs, and quality records.
• Ability and willingness to be onsite and support manufacturing operations during off-shift hours, including weekday and weekend night shifts, as required to execute validation activities, and support commercial manufacturing schedules.

Day to Day Responsibilities:
The engineer provides technical support for commercial manufacturing through equipment and process troubleshooting, critical process parameter optimization, deviation investigations, and continuous improvement. The role is responsible for authoring and executing engineering studies, characterization, Commissioning, Qualification, and Validation (CQV) protocols, and technical summary reports to support compliant and reliable manufacturing operations.
Key documentation responsibilities include authoring, executing, and/or approving technical documentation, including:

• Characterization test protocols and reports
• Commissioning, Qualification, and Validation (CQV) test protocols and reports for manufacturing equipment, computerized systems, and processes
• Engineering studies and technical assessments
• Validation Master Plans, Validation Plans, and Summary Reports
• Technical reports supporting equipment lifecycle management, process improvements, technology transfers, and new product introductions (NPI)

Basic Qualifications:
Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience
Red Flags:

• Candidate lacks demonstrated hands-on experience leading Commissioning, Qualification, and Validation (CQV) activities within a GMP biotechnology or pharmaceutical manufacturing environment, including authoring and executing characterization, validation, and engineering test protocols, as well as preparing technical reports to support equipment/system qualification and process validation.
• Candidate is unable to work autonomously or demonstrate strong technical ownership of commercial manufacturing support, including equipment and process troubleshooting, critical process parameter optimization, deviation investigations, root cause analysis, and the ability to implement data-driven process improvements in a regulated manufacturing environment.
• Candidate is unwilling or unable to work onsite to support commercial manufacturing during off-shift operations, including weekday and weekend night work, or lacks the flexibility required to execute validation activities and provide engineering support during critical manufacturing, qualification, and project schedules.

Interview process:
Microsoft Teams Virtual Interviews (1:1 or Panel)
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.