Consulting for Biotech and Pharma Companies with focus on vaccines
TS Pharma Consulting, based in Überlingen, Germany, leverages 15+ years of biotech and pharma industry experience to offer expert consulting and contracting services, specializing in vaccines. We are your trusted partner for comprehensive solutions.
MS&T services
Ranging from document authoring to developing and executing strategies for process validation.
Problem resolution
We help you to overcome challenges such as deviations by applying our experience to investigate issues and resolve them promptly.
Bridging bottlenecks
You currently have project peaks and do not know how to handle your orders. We help you competently!
TS Pharma Consulting
- we deliver what we promise
TS Pharma Consulting is a consulting company for the biotech and pharma industry, located in Überlingen at Lake Constance, Germany.
With over 15 years of practical experience in various production and engineering departments, we support you in providing expert knowledge as consultants and contractors. Our focus is on biotech and pharmaceutical companies in the areas of biotechnology, vaccines, nanoparticles, cytostatics and small and large molecules. The expertise offered covers the entire range from basic engineering to project management to technical writing support for regulatory submissions.
As a practice partner we help you to implement your requirements conscientiously. Please do not hesitate to contact us.
Our Services
Our project management offers customized solutions
Our project management service offers customized solutions that include qualification, process development, implementation and technology transfer.
We take over the management and coordination of these critical phases in your projects. With our many years of experience in the biotech and pharmaceutical industries, we ensure smooth qualification, effective process development and implementation, and successful technology and process transfers.
Rely on us to complete your projects in time and within budget while delivering the highest quality and industry standards.
Process Engineering - support throughout your project lifecycle
We guide you from process development to regulatory filing for technical matters, with extensive experience in Drug Product (DP) relevant processes such as filter validation and visual inspection. Our services also encompass material and documentation flow development, waste management, cross-contamination prevention concepts, shift concept development, and training.
We provide solutions for process comparability and offer engineering support for specifying production equipment. Our qualification support ensures compliance with industry standards.
When it comes to seamless tech transfers between sites, we are your trusted partner. We create and implement aseptic process simulations and author GMP documentation, including SOPs, risk analyses, protocols, and technical filing documents.
Continuous improvement to optimize operations
We excel in CAPA management, identifying, addressing, and preventing issues to enhance quality and compliance.
Change management is another forte; we can efficiently implement changes while maintaining operational excellence. Investigation management is our strength, as we delve deep into issues, uncover root causes, and implement effective solutions. Deviation management ensures processes stay on track and in compliance, even when deviations occur.
We streamline documentation processes for accuracy and efficiency and enhance facility layouts for optimal workflow and safety. Our expertise also extends to optimizing production processes for efficiency, cost-effectiveness, and superior product quality.
Our operational process
01
In the first step, we take a look at your current situation in order to provide you with the best possible advice. We review structures, framework conditions and systems.
02
We advise you which steps are necessary to implement your project and discuss the further project process with you.
03
Now we can implement follow-up processes, documents and systems tailored to your needs and make your project a success.
Our team
- operational experience
Tim Schulz, the founder of our team, boasts over 15 years of experience in the pharmaceutical industry, collaborating with renowned global companies. Over 100 projects have enriched his expertise, spanning from fundamental design qualification to regulatory documentation and final approval.
Each member of our experienced team has at least a decade of hands-on experience in global projects. As a consultancy we support our customers worldwide and are fluent in German, English and Mandarin.
Collectively, we excel in development, production, project management, process refinement, and product quality. This wealth of practical knowledge empowers us to not only understand the actions necessary for client success but also to steer clear of pitfalls.
Driven by this vision, Tim Schulz founded our consultancy, aiming to impart our collective wisdom to pharmaceutical and biotech enterprises.
Tim Schulz
FounderDipl. Ing. for pharmaceutical engineering
Johannes Dörl
Sr. Process & Project Manager
Stanley Yong
容耀祥
Sr. Project & Process Consultant Manager
Lea Schulz
Office ManagerFrequently asked
- questions
Do you have any further questions? We are always available by phone during our business hours. Or conveniently use our contact form – we will get back to you as soon as possible.
We specialize in a wide range of areas within the biotech and pharmaceutical industries, with a focus on vaccines. Our expertise includes biotechnology, vaccines, nanoparticles, cytostatics and small molecules.
TS Pharma Consulting differentiates itself through its extensive experience, specialization in vaccines, and its commitment to delivering on promises. Our hands-on approach, from basic engineering to regulatory support, sets us apart as a comprehensive and reliable consulting partner.
Your partner for the Biotech and Pharma industry
Our Location
Überlingen at Lake Constance, Germany
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