Pharma Process
Engineering
ZETA implements highly complex pharma projects in the shortest possible time
Plan project nowBenefits with ZETA Process Engineering
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1
Time-to-Market:Get to market faster with us!
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2
Engineering expertise:Process & Plant Engineering from a single source.
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3
Cost control:Transparency through CAPEX project management.
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4
Security and sustainability in the planning process.
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5
Experience in plant engineering:Integrated engineering for pharma & biotech.
Pharma project management
in record time
Time to market: With ZETA's project management
up to 50 % faster to market.
Process & Plant Engineering
Different teams work with you on an interdisciplinary basis in every phase of the process!
Project
Managers
Managers
Process
Engineer
Engineer
HVAC -
BMS/EMS
Engineers
BMS/EMS
Engineers
Mathematical
Analysts
Analysts
Cleanroom
Experts
Experts
Your
company!
company!
Automation
Expert
Expert
Biotechnology
Expert
Expert
Civil
Engineers
Engineers
EIC Engineers
Mechanical
Engineer
Engineer
Logistics
low
moderate
strong
very strong
Engineering Solutions for
pharma & biotech:
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API production
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mAb production
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Blood plasma processing
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Vaccine production
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Aseptic products
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Emulsions
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Chemical synthesis
Starter Package
Pharma Engineering
It all starts with your vision: We take over the planning and implementation of GMP-compliant process engineering.
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1
Process Improvement
From the "actual" model to the "target" model: Together with you, we analyze your current process and find out where the technical challenges lie and how we can solve them. -
2
Process Development
Together with you, we will develop a technological solution that is tailor-made for your needs and your process. -
3
Expert Workshop
We work out ways to find solutions and possible scenarios in a joint workshop. -
4
Creation of the Scope of Delivery
We create the follow-up documentation (PFD and URS), schedules, budgeting, results and show recommendations or alternative options for you. -
5
Concluding Meeting
We define the next common steps in a final meeting.
Contact: Daniel Maier
Senior Director Engineering & Services
We would be happy
to advise you personally!
Scale Up & Down
in the pharmaceutical industry
GMP-compliant scaling: From the laboratory to industrial production - and back again!
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Laboratory
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Pilot
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Production
Numerous planning steps are necessary from the laboratory to industrial production when developing active ingredients. Only through a thorough understanding of the process can errors and additional costs be avoided and rapid project implementation guaranteed.
Our Pillars of Success
in process engineering
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1
Time Management
Faster project execution for quick market introduction. -
2
Technical Planning
GMP-compliant production meets all requirements of the approval authorities. -
3
Economic Planning
Efficient and well thought-out project calculation for the management of large pharma CAPEX projects.
Customer statement
Thanks for the good and most of all solution-oriented collaboration…1700 documents were created based on a schedule that was steady for really most parts throughout the entire project. In particular the quality of the 3D Model deserves to be mentioned. The performance – with only very few exceptions due to collisions in the tightest of spaces – was successfully carried out across trades and – above all – collision-free…
Gerhard Gatterwe, OCTAPHARMA
FREQUENTLY ASKED QUESTIONS ABOUT
PROCESS ENGINEERING & PHARMA CAPEX PROJECTS
What is process engineering in the pharmaceutical industry?
Process engineering in the pharmaceutical industry encompasses the development, optimization and scaling of production processes for drugs and biopharmaceuticals. It ensures that GMP standards are adhered to, production processes are designed efficiently and regulatory requirements are met.
What are pharma CAPEX projects and why are they important?
Pharma CAPEX projects relate to investments in plants, production facilities and process optimization. They are crucial for the industrialization of new active ingredients, the implementation of innovative process technologies and compliance with regulatory requirements.
How does scale-up and scale-down work in the pharmaceutical industry?
In scale-up, a biotechnological or pharmaceutical process is transferred from smaller scales (laboratory, pilot) to industrial production in order to manufacture larger quantities. Scale-down involves replicating industrial processes on a smaller scale in order to optimize them in research & development or for test runs.
Why is GMP-compliant scaling important in process engineering?
GMP-compliant scaling ensures that production processes comply with strict GMP guidelines from the laboratory phase through pilot scale to industrial production. This ensures safety, quality, reproducibility and regulatory compliance.
What advantages does integrated engineering offer the pharmaceutical industry?
Integrated Engineering combines Process Engineering, Plant Engineering and Bioprocess Technology to implement pharmaceutical CAPEX projects efficiently, GMP-compliant and economically. Thanks to integrated planning and interdisciplinary collaboration, companies can shorten time-to-market, make optimum use of resources and take regulatory requirements into account at an early stage.
Discover
more ZETA offers
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Service -
ServiceBuilding EquipmentWe combine TGA, HVAC, clean room and the entire process technology under one roof!
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Solutions
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