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Project Developer

Full-time

ZETA

ZETA is a globally active solutions provider that supports pharmaceutical and biotech companies in bringing vital medicines such as insulin infusions and cancer treatments to market faster and more an innovation leader we combine technical expertise with digital excellence covering everything from planning and construction to automation and qualification of customized process addition we take on full responsibility for complex projects as an EPCMV partner drive digital transformation and develop sustainable strategies for decarbonization.

Project Developer

Location: King of Prussia

Contract: Full-time employee

Job Overview

Job Overview

The Project Developer is responsible for developing technical concepts process solutions and engineering deliverables during early project phases for pharmaceutical biotechnology and life sciences. The role translates client requirements and user requirements specifications into practical project concepts technical scopes and proposal-ready engineering packages.

Working closely with project managers process engineers automation engineers mechanical engineers electrical engineers fabrication and delivery teams and external design partners the Project Developer helps define project scope evaluate technical alternatives identify risks and support successful project handover into execution.

Key Responsibilities

Project Development and Concept Engineering

  • Develop conceptual and basic engineering solutions for pharmaceutical biotech life sciences.
  • Analyze client requirements user requirements specifications (URS) technical design criteria site constraints and project objectives.
  • Define process and facility concepts including process flows equipment requirements utility interfaces layout considerations and project assumptions.
  • Evaluate technical options identify engineering risks compare alternative concepts and recommend practical cost-effective project solutions.
  • Support feasibility studies conceptual design studies basic engineering packages and front-end engineering design (FEED) activities.
  • Coordinate closely with process mechanical automation electrical fabrication and delivery teams during project development.
  • Coordinate with external partners for HVAC MEP architectural civil and other specialist design disciplines as required.
  • Ensure technical concepts are aligned across engineering disciplines stakeholder expectations client requirements and project execution strategy.
  • Support multidisciplinary design packages technical workshops constructability reviews and project transition from development to execution.

Your profile

Required Qualifications

Education

  • Bachelors or masters degree in Chemical Engineering Process Engineering Mechanical Engineering Electrical Engineering Biotechnology Engineering or a related engineering discipline.

Experience

  • 5 years of engineering and/or project execution experience in pharmaceutical biotechnology life sciences.
  • Experience in conceptual design basic engineering project development proposal engineering or FEED activities.
  • Experience in full execution of capital projects engineering studies technical proposals or multidisciplinary project scopes.
  • Familiarity with GMP-regulated environments hygienic design expectations and regulated manufacturing facilities is preferred.

Technical Skills

  • Strong understanding of process engineering principles process systems unit operations and manufacturing facility requirements.
  • Baseline understanding of mechanical electrical automation utilities HVAC MEP and facility engineering interfaces.
  • Knowledge of pharmaceutical and biotechnology manufacturing processes including GMP equipment and environments.
  • Experience with process flow diagrams (PFDs) piping and instrumentation diagrams (P&IDs) equipment sizing process descriptions and design basis documentation.
  • Proficiency with Microsoft Office applications for technical documentation proposal development estimates and stakeholder communication.
  • Familiarity with CAD platforms such as AutoCAD or similar engineering tools; BIM or 3D model review experience is an advantage.
  • Understanding of project execution methodologies engineering workflows quality review processes and project handover requirements.
  • Knowledge of GMP FDA EMA and related regulatory frameworks is preferred.

Personal Competencies

  • Strong analytical problem-solving and decision-support skills.
  • Excellent communication presentation and technical writing abilities.
  • Customer-focused mindset with the ability to translate requirements into practical engineering solutions.
  • Ability to manage multiple priorities deadlines stakeholders assumptions and open technical issues.
  • Team-oriented working style with strong collaboration across engineering disciplines and business functions.
  • Proactive innovative and solution-driven approach to early-phase project development.
  • High attention to detail and commitment to quality accuracy and traceable engineering documentation.

We offer

A hybrid schedule with 3 days in office 2 remote and free coffee

Medical Dental & Vision Health Benefits

Competitive PTO & vacation

401K with 5% employer match of annual salary

Travel & training

A hybrid schedule with 3 days in office 2 remote and free coffee

Medical Dental & Vision Health Benefits

Competitive PTO & vacation

401K with 5% employer match of annual salary

Travel & training

Competitive PTO & vacation

  • A hybrid schedule with 3 days in office 2 remote and free coffee

  • Medical Dental & Vision Health Benefits

  • Competitive 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

ZETA is a globally active solutions provider that supports pharmaceutical and biotech companies in bringing vital medicines such as insulin infusions and cancer treatments to market faster and more an innovation leader we combine technical expertise with digital excellence covering everything from planning and construction to automation and qualification of customized process addition we take on full responsibility for complex projects as an EPCMV partner drive digital transformation and develop sustainable strategies for decarbonization.

Project Developer

Location: King of Prussia

Contract: Full-time employee

Your tasks

Job Overview

The Project Developer is responsible for developing technical concepts process solutions and engineering deliverables during early project phases for pharmaceutical biotechnology and life sciences. The role translates client requirements and user requirements specifications into practical project concepts technical scopes and proposal-ready engineering packages.

Working closely with project managers process engineers automation engineers mechanical engineers electrical engineers fabrication and delivery teams and external design partners the Project Developer helps define project scope evaluate technical alternatives identify risks and support successful project handover into execution.

Key Responsibilities

Project Development and Concept Engineering

  • Develop conceptual and basic engineering solutions for pharmaceutical biotech life sciences.
  • Analyze client requirements user requirements specifications (URS) technical design criteria site constraints and project objectives.
  • Define process and facility concepts including process flows equipment requirements utility interfaces layout considerations and project assumptions.
  • Evaluate technical options identify engineering risks compare alternative concepts and recommend practical cost-effective project solutions.
  • Support feasibility studies conceptual design studies basic engineering packages and front-end engineering design (FEED) activities.
  • Coordinate closely with process mechanical automation electrical fabrication and delivery teams during project development.
  • Coordinate with external partners for HVAC MEP architectural civil and other specialist design disciplines as required.
  • Ensure technical concepts are aligned across engineering disciplines stakeholder expectations client requirements and project execution strategy.
  • Support multidisciplinary design packages technical workshops constructability reviews and project transition from development to execution.

Your profile

Required Qualifications

Education

  • Bachelors or masters degree in Chemical Engineering Process Engineering Mechanical Engineering Electrical Engineering Biotechnology Engineering or a related engineering discipline.

Experience

  • 5 years of engineering and/or project execution experience in pharmaceutical biotechnology life sciences.
  • Experience in conceptual design basic engineering project development proposal engineering or FEED activities.
  • Experience in full execution of capital projects engineering studies technical proposals or multidisciplinary project scopes.
  • Familiarity with GMP-regulated environments hygienic design expectations and regulated manufacturing facilities is preferred.

Technical Skills

  • Strong understanding of process engineering principles process systems unit operations and manufacturing facility requirements.
  • Baseline understanding of mechanical electrical automation utilities HVAC MEP and facility engineering interfaces.
  • Knowledge of pharmaceutical and biotechnology manufacturing processes including GMP equipment and environments.
  • Experience with process flow diagrams (PFDs) piping and instrumentation diagrams (P&IDs) equipment sizing process descriptions and design basis documentation.
  • Proficiency with Microsoft Office applications for technical documentation proposal development estimates and stakeholder communication.
  • Familiarity with CAD platforms such as AutoCAD or similar engineering tools; BIM or 3D model review experience is an advantage.
  • Understanding of project execution methodologies engineering workflows quality review processes and project handover requirements.
  • Knowledge of GMP FDA EMA and related regulatory frameworks is preferred.

Personal Competencies

  • Strong analytical problem-solving and decision-support skills.
  • Excellent communication presentation and technical writing abilities.
  • Customer-focused mindset with the ability to translate requirements into practical engineering solutions.
  • Ability to manage multiple priorities deadlines stakeholders assumptions and open technical issues.
  • Team-oriented working style with strong collaboration across engineering disciplines and business functions.
  • Proactive innovative and solution-driven approach to early-phase project development.
  • High attention to detail and commitment to quality accuracy and traceable engineering documentation.

Under the motto Lets Engineer Your Career Together we are looking forward to receiving your application!

ZETA USA Inc.
2200 Renaissance Blvd Ste. 170 King of Prussia PA 19406

Required Experience:

IC

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