Senior Process Engineer
King of Prussia, PA - USA
Job Summary
ZETA is a global engineering and technology partner serving pharmaceutical and biopharma companies. With over 30 years of experience we specialize in process engineering automation and GMP-compliant systems to help deliver life-saving therapies.
Position Summary
The Senior Process Engineer is responsible for leading process design and engineering activities for ZETAs biopharmaceutical client projects. This role supports the development of process systems including upstream downstream blood plasma fractionation ADCs and cell and gene therapy applications. The Senior Process Engineer collaborates with cross-functional engineering teams to deliver high-quality GMP-compliant solutions.
| Location: King of Prussia | Contract: Full-time employee | Start: 27.10.2026 |
Duties and Responsibilities |
- Accountable for delivering the process engineering scope on time on budget and in accordance with quality and compliance requirements.
- Prepare and review process engineering documentation including PFDs P&IDs and mass/energy balances.
- Specify and design process equipment such as vessels mixing systems filtration skids and related components.
- Develop User Requirements Specifications (URS) and Functional Specifications.
- Lead and execute start-up and commissioning activities including FAT and SAT.
- Provide process troubleshooting and technical support to internal and external stakeholders.
- Coordinate with automation mechanical and project management teams to ensure alignment across engineering disciplines.
- Develop CIP/SIP strategies including cycle design testing and optimization.
Required Qualifications |
- Bachelors degree in Engineering or related technical discipline.
- Minimum 10 years of experience in the Biotech/Pharmaceutical industry.
- Knowledge of GMP requirements and biopharmaceutical process systems.
- Experience with bioprocess unit operations such as buffer/media prep upstream or downstream processing.
- Prior experience supporting capital projects.
- Hybrid work model with three onsite days per week at the King of Prussia office.
- Travel up to 30% including domestic and international assignments as needed for project execution FAT/SAT or client support.
- Ability to work in an office client sites and manufacturing environments as needed.
Free coffee & Teas | Medical Dental & Vision Health Benefits & HSA & Short-term Disability | European-style PTO & vacation |
401K with 5% employer match of annual salary | Travel & training |
Free coffee & Teas | Medical Dental & Vision Health Benefits & HSA & Short-term Disability |
European-style PTO & vacation | 401K with 5% employer match of annual salary |
Travel & training |
European-style PTO & vacation
Free coffee & Teas
Medical Dental & Vision Health Benefits & HSA & Short-term Disability
European-style PTO & vacation
- 401K with 5% employer match of annual salary
- Travel & training
Your application will processed by Nancy Lowell |
2200 Renaissance Blvd Ste. 170 King of Prussia PA 19406
ZETA is a global engineering and technology partner serving pharmaceutical and biopharma companies. With over 30 years of experience we specialize in process engineering automation and GMP-compliant systems to help deliver life-saving therapies.
Position Summary
The Senior Process Engineer is responsible for leading process design and engineering activities for ZETAs biopharmaceutical client projects. This role supports the development of process systems including upstream downstream blood plasma fractionation ADCs and cell and gene therapy applications. The Senior Process Engineer collaborates with cross-functional engineering teams to deliver high-quality GMP-compliant solutions.
| Location: King of Prussia | Contract: Full-time employee | Start: 27.10.2026 |
Your tasks |
- Accountable for delivering the process engineering scope on time on budget and in accordance with quality and compliance requirements.
- Prepare and review process engineering documentation including PFDs P&IDs and mass/energy balances.
- Specify and design process equipment such as vessels mixing systems filtration skids and related components.
- Develop User Requirements Specifications (URS) and Functional Specifications.
- Lead and execute start-up and commissioning activities including FAT and SAT.
- Provide process troubleshooting and technical support to internal and external stakeholders.
- Coordinate with automation mechanical and project management teams to ensure alignment across engineering disciplines.
- Develop CIP/SIP strategies including cycle design testing and optimization.
Your profile |
- Bachelors degree in Engineering or related technical discipline.
- Minimum 10 years of experience in the Biotech/Pharmaceutical industry.
- Knowledge of GMP requirements and biopharmaceutical process systems.
- Experience with bioprocess unit operations such as buffer/media prep upstream or downstream processing.
- Prior experience supporting capital projects.
- Hybrid work model with three onsite days per week at the King of Prussia office.
- Travel up to 30% including domestic and international assignments as needed for project execution FAT/SAT or client support.
- Ability to work in an office client sites and manufacturing environments as needed.
Required Experience:
Senior IC
About Company
Der biopharmazeutische Markt weist hohe Wachstumsraten auf und weltweit werden Produktionskapazitäten zur Herstellung hochwertiger Medikamente aufgebaut. Die ZETA Gruppe hat sich in diesem herausfordernden Umfeld als verlässlicher und global agierender Engineering Partner etabliert. Z ... View more