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Senior Process Engineer

ZETA


Job Location:

King of Prussia, PA - USA

Monthly Salary: Not provided by the employer
Posted: 19 October 2026 (4 days ago)
Application Deadline: 16 January 2027
Vacancies: 1 Vacancy

Job Summary

About Us

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.

Senior Process Engineer
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.
Preferred Qualifications
  • Experience with bioprocess unit operations such as buffer/media prep upstream or downstream processing.
  • Prior experience supporting capital projects.
Work Environment & Physical Requirements
  • 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.
We offer

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
Under the motto Lets Engineer Your Career Together we are looking forward to receiving your application!
Your application will
processed by
Nancy Lowell
Evolution of Technology find more here:
ZETA USA Inc.
2200 Renaissance Blvd Ste. 170 King of Prussia PA 19406
About Us

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.

Senior Process Engineer
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.
Preferred Qualifications
  • Experience with bioprocess unit operations such as buffer/media prep upstream or downstream processing.
  • Prior experience supporting capital projects.
Work Environment & Physical Requirements
  • 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.
Under the motto Lets Engineer Your Career Together we are looking forward to receiving your application!

Required Experience:

Senior IC


About Company

Company Logo

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

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