What are the responsibilities and job description for the Senior Packaging Validation Engineer, Biotech GMP Final Drug Product (JP14454) position at 3 Key Consulting?
Job Title: Senior Packaging Validation Engineer, Biotech GMP Final Drug Product (JP14454)
Location: New Albany, Oh 43054
Business Unit: Site Process Development
Employment Type: Contract
Duration: 2 years with possible extension or conversion to FTE
Rate: $53 - $63/hour (DOE) - W2 with benefits
Posting Date: 8/28/2025.
3 Key Consulting is hiring! We are recruiting a Senior Validation Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
The Senior Validation Engineer position reports into the Sr. Manager of Validation. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations.
Location Options: 100% Site Presence Required. The position is expected to travel for approximately 10%.
Job Description & Responsibilities:
The Senior Validation Engineering will support the development and implementation of automated and semi-automated combination product assembly equipment initiatives as part of the Finished Drug Product (FDP) product portfolio at the Ohio manufacturing site. The position is a key role in the Process Development team where the candidate must manage and/or apply extensive technical expertise (characterization, validation and troubleshooting) in the validation of combination products. This position also requires the application of advance and diverse engineering principles to more than one area of engineering (process, unit operations, equipment, devices and materials) in complex process optimization, scale up and manufacturing support projects.
Output:
Key responsibilities will include supporting the packaging C&Q activities of the product portfolio to AOH. Additional responsibilities will include the provision of technical operations support for the continuous improvement of device assembly and packaging line capacity and performance, and advisory of technical improvement projects. The Sr. Validation Engineer must ensure effective communication throughout the Ohio commercial site and network with all stakeholders and deliver on technical deliverables.
Relationship:
The Senior Validation Engineering is expected to build on the network expertise across the company commercial and clinical operations for product assembly, label and packaging. The position is expected to leverage this network in support of GMP technical expertise, performance trending, equipment standardization and troubleshooting/process
The successful candidate will have:
Value proposition: Unique industry opportunity Networking
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
Why is the Position Open?
Supplement additional workload on team
Interview Process:
Initial screening with hiring manager
Final interview panel with 3 interviewers
We invite qualified candidates to send your resume to recruiting@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.
Location: New Albany, Oh 43054
Business Unit: Site Process Development
Employment Type: Contract
Duration: 2 years with possible extension or conversion to FTE
Rate: $53 - $63/hour (DOE) - W2 with benefits
Posting Date: 8/28/2025.
3 Key Consulting is hiring! We are recruiting a Senior Validation Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
The Senior Validation Engineer position reports into the Sr. Manager of Validation. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations.
Location Options: 100% Site Presence Required. The position is expected to travel for approximately 10%.
Job Description & Responsibilities:
The Senior Validation Engineering will support the development and implementation of automated and semi-automated combination product assembly equipment initiatives as part of the Finished Drug Product (FDP) product portfolio at the Ohio manufacturing site. The position is a key role in the Process Development team where the candidate must manage and/or apply extensive technical expertise (characterization, validation and troubleshooting) in the validation of combination products. This position also requires the application of advance and diverse engineering principles to more than one area of engineering (process, unit operations, equipment, devices and materials) in complex process optimization, scale up and manufacturing support projects.
Output:
Key responsibilities will include supporting the packaging C&Q activities of the product portfolio to AOH. Additional responsibilities will include the provision of technical operations support for the continuous improvement of device assembly and packaging line capacity and performance, and advisory of technical improvement projects. The Sr. Validation Engineer must ensure effective communication throughout the Ohio commercial site and network with all stakeholders and deliver on technical deliverables.
Relationship:
The Senior Validation Engineering is expected to build on the network expertise across the company commercial and clinical operations for product assembly, label and packaging. The position is expected to leverage this network in support of GMP technical expertise, performance trending, equipment standardization and troubleshooting/process
The successful candidate will have:
- Knowledge of high-speed, highly automated secondary packaging operations
- Knowledge of the validation of equipment such as PFS assembly, cartoners, vision systems
- Experience in writing protocols
- Experience in executing protocols
- Capable of executing multiple projects
- Communication skills and ability to work with other people
- Bring innovative solutions for continuous process improvement
- Experience with Kneat
- Experience with MiniTab is a plus
- packaging validation experience
- knowledge of packaging equipment
- protocol generation and execution
- writing and executing validation protocols.
Value proposition: Unique industry opportunity Networking
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
Why is the Position Open?
Supplement additional workload on team
Interview Process:
Initial screening with hiring manager
Final interview panel with 3 interviewers
We invite qualified candidates to send your resume to recruiting@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.
Salary : $53 - $63