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The biopharmaceutical market is showing high growth rates and production capacities for the manufacture of high-quality drugs with increasing demand worldwide. In this challenging environment, the ZETA Group has established itself as a reliable and globally active engineering partner. ZETA designs, builds, automates and qualifies equipment for aseptic liquid production processes in the biotech and pharmaceutical industries. Biopharmaceutical agents such as anticancer agents, insulin, vaccines, infusions and the like are produced on these highly complex "tailor-made" plants. As an international, fast-growing company, ZETA relies above all on its dedicated employees.

Senior Process Engineer

Location: King of Prussia Contract: Full-time employee Start: As of now

Your tasks

    • Responsible for process engineering of aseptic process equipment and utility systems ranging from concept design to CQV.
    • Effective communication with internal and external project team members across all disciplines.
    • Support Project Manager with man-hour planning, workflow management, scope control and project scheduling for the process engineering scope of work on intermediate level projects.
    • Leading and coordinating process engineering teams
    • Independent development of the following process engineering deliverables and activities:
      • Customer communication to establish process steps and requirements.
      • Creation, review, and implementation of process specific URS requirements.
      • PFDs
      • Process descriptions, batch planning and CIP/SIP concept development
      • P&IDs
      • Process calculations including line size/pressure drop, media consumption lists, mass/energy balances,
      • Dimensioning of equipment including vessels, pumps, heat exchangers, and filter housings.
      • Specification and list creation.
      • EHS risk analysis
      • Review of 3D models
      • Development and documentation of system functionality including superior alarms and interlocks, control module definition, phase functional design specifications, recipe development.
      • Adaption of existing SW-FAT/FAT/SAT test protocols to meet specific project and customer requirements.
      • Support SW-FATs
      • Execute Dynamic commissioning, FATs and SATs
    • Compliance with SOPs, standards and legal regulations
    • Contribution to the further development and implementation of standards of the department
    • Observation and identification of new trends and technologies and their application.
    • Support Bid Manager with proposal development including hours forecasting, timeline development and cost estimation.
    • One time onboarding training in Vienna AT for 1-3 months. (Experience level dependent)
    • Up to 30% travel for commissioning/FAT/SAT activities.
 

Your profile

  • Professionally and technical trained process engineer.
  • Batchelor’s degree in Chemical Engineering. (Alternate degrees considered)
  • Minimum of 5 years’ experience in bioprocessing or biopharmaceutical manufacturing industry. Equipment design focus is preferred.
  • Working knowledge of GMP & GEP procedures and project management.
  • Understanding of design, fabrication, documentation and testing conventions in pharmaceutical/biopharmaceutical industries.
  • Comprehensive knowledge of and skills in MS-Office (especially Excel) and ERP systems experience.
  • Excellent communication skills (written and spoken) in English (German is preferred but not required)
  • A keen sense of responsibility, self-motivation, team spirit, flexibility, accuracy, quality awareness, target orientation and cooperation.
  • Ability to work autonomously and as part of a cross-functional team
  • Self-assured and comfortable working in customer-facing situations.
  • Experience managing process engineering teams is preferred.
  • Ability to travel internationally.
  •  

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 "Let's Engineer Your Career Together" we are looking forward to receiving your application!
Your application will
processed by
Nancy Lowell
 
The biopharmaceutical market is showing high growth rates and production capacities for the manufacture of high-quality drugs with increasing demand worldwide. In this challenging environment, the ZETA Group has established itself as a reliable and globally active engineering partner. ZETA designs, builds, automates and qualifies equipment for aseptic liquid production processes in the biotech and pharmaceutical industries. Biopharmaceutical agents such as anticancer agents, insulin, vaccines, infusions and the like are produced on these highly complex "tailor-made" plants. As an international, fast-growing company, ZETA relies above all on its dedicated employees.

Senior Process Engineer

Location: King of Prussia Contract: Full-time employee Start: As of now

Your tasks

    • Responsible for process engineering of aseptic process equipment and utility systems ranging from concept design to CQV.
    • Effective communication with internal and external project team members across all disciplines.
    • Support Project Manager with man-hour planning, workflow management, scope control and project scheduling for the process engineering scope of work on intermediate level projects.
    • Leading and coordinating process engineering teams
    • Independent development of the following process engineering deliverables and activities:
      • Customer communication to establish process steps and requirements.
      • Creation, review, and implementation of process specific URS requirements.
      • PFDs
      • Process descriptions, batch planning and CIP/SIP concept development
      • P&IDs
      • Process calculations including line size/pressure drop, media consumption lists, mass/energy balances,
      • Dimensioning of equipment including vessels, pumps, heat exchangers, and filter housings.
      • Specification and list creation.
      • EHS risk analysis
      • Review of 3D models
      • Development and documentation of system functionality including superior alarms and interlocks, control module definition, phase functional design specifications, recipe development.
      • Adaption of existing SW-FAT/FAT/SAT test protocols to meet specific project and customer requirements.
      • Support SW-FATs
      • Execute Dynamic commissioning, FATs and SATs
    • Compliance with SOPs, standards and legal regulations
    • Contribution to the further development and implementation of standards of the department
    • Observation and identification of new trends and technologies and their application.
    • Support Bid Manager with proposal development including hours forecasting, timeline development and cost estimation.
    • One time onboarding training in Vienna AT for 1-3 months. (Experience level dependent)
    • Up to 30% travel for commissioning/FAT/SAT activities.

Your profile

  • Professionally and technical trained process engineer.
  • Batchelor’s degree in Chemical Engineering. (Alternate degrees considered)
  • Minimum of 5 years’ experience in bioprocessing or biopharmaceutical manufacturing industry. Equipment design focus is preferred.
  • Working knowledge of GMP & GEP procedures and project management.
  • Understanding of design, fabrication, documentation and testing conventions in pharmaceutical/biopharmaceutical industries.
  • Comprehensive knowledge of and skills in MS-Office (especially Excel) and ERP systems experience.
  • Excellent communication skills (written and spoken) in English (German is preferred but not required)
  • A keen sense of responsibility, self-motivation, team spirit, flexibility, accuracy, quality awareness, target orientation and cooperation.
  • Ability to work autonomously and as part of a cross-functional team
  • Self-assured and comfortable working in customer-facing situations.
  • Experience managing process engineering teams is preferred.
  • Ability to travel internationally.
  •  

Under the motto "Let's Engineer Your Career Together" we are looking forward to receiving your application!
Apply now and become part of the ZETA-Team!