ZETA

Project Developer

ZETA  •  Raleigh, NC (Hybrid)  •  1 hour ago
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Job Description

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 efficiently. As an innovation leader, we combine technical expertise with digital excellence, covering everything from planning and construction to automation and qualification of customized process systems. In 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: Raleigh Contract: Full-time employee Start: 05.10.2026

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. This role will also include supporting the sales and marketing team with technical expertise during customer discussions.

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

  • Bachelor's or master’s 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; 3 days in office, 2 remote, and free coffee in office

Medical, Dental, & Vision Health Benefits

Competitive PTO & vacation

401K with 5% employer match of annual salary

Travel & training

Our Zeta Values

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

Medical, Dental, & Vision Health Benefits

Competitive PTO & vacation

401K with 5% employer match of annual salary

Travel & training

Our Zeta Values

Competitive PTO & vacation

  • A hybrid schedule; 3 days in office, 2 remote, and free coffee in office
  • Medical, Dental, & Vision Health Benefits
  • Competitive PTO & vacation
  • 401K with 5% employer match of annual salary
  • Travel & training
  • Our Zeta Values

Under the motto "Let's Engineer Your Career Together" we are looking forward to receiving your application!

Your application will

processed by

Nancy Lowell

Apply now

Evolution of Technology – find more here: www.zeta.com, us.zeta.com

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 efficiently. As an innovation leader, we combine technical expertise with digital excellence, covering everything from planning and construction to automation and qualification of customized process systems. In 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: Raleigh Contract: Full-time employee Start: 05.10.2026

Your tasks

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. This role will also include supporting the sales and marketing team with technical expertise during customer discussions.

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

  • Bachelor's or master’s 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 "Let's Engineer Your Career Together" we are looking forward to receiving your application!

Apply now and become part of the ZETA-Team!

ZETA

About ZETA

The ZETA Group is an end-to-end solution provider operating globally and specializing in the design, construction, automation, digitization and qualification of customer-specific biopharmaceutical systems for aseptic process solutions.

ZETA provides support after commissioning of the process equipment through targeted ramp-up as well as service and maintenance along the entire product lifecyle. True to the principle of continuous improvement, ZETA guides customers during process and system optimization as well as operator training.

As general planners (EPCM), ZETA manages major, high-complexity pharma projects and specifically reduces interfaces—from the planning and construction of the process system through the cleanroom design up to the technical building infrastructure. This design-build approach accelerates the project execution time by up to 50% and leads to creation of value earlier in the customer’s capex projects.

In the field of digitization, ZETA’s fully integrated digital value chain—from engineering through qualification and operator management—has established the company as an innovation driver in the pharma and biotech industry. ZETA is also actively taking steps towards a more sustainable future for the entire industry: By holistic decarbonization strategies that reduce targeted emissions during the biopharmaceutical manufacturing process.

Your reliable partner for biopharmaceutical projects:

• EPCMv contractor

• Plant engineering

• HVAC-, cleanroom and BMS/EMS design

• Decarbonization

• Automation

• Digitalisation

• Qualification

• Maintenance & Upgrades

• Research & Development

Legal Notice: https://www.zeta.com/legal-notice/

Data Protection: https://www.zeta.com/data-protection/

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Lieboch, AT
Year Founded
1989
Website
zeta.com
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