Dr. Andreas Wenng

cGMP Production Specialist and Senior Manager

"Applying best practices in tailor-made and speed-based manufacturing processes is the future." 

I support 3R LifeScience with my expertise and knowledge of cGMP production of medical devices and pharmaceutical products.

Over the past 20 years, I have worked for international organisations in senior roles where I built, reorganised and optimised production processes for the Life Science industry all over the world. I have successfully implemented lean processes and applied realistic and practical Six Sigma approaches to combine highest quality standards with reduction in production time, waste and costs.

Today, one challenge of the pharmaceutical industry is the translation of the FDA Quality-by-Design (QbD) initiative and risk-based approaches in pharmaceutical Development and Manufacturing. Time and efforts are made to develop infrastructures that combine quality attributes and product specifications with process parameters and control measures. I will support your organisation to succeed in this by implementing Process Analytical Technologies (PAT) and validating scale-up and production processes.

I believe that also start-up companies should understand the risks associated with transferring R&D processes to pilot production and final manufacturing. For this, I support decision-makers to put the right processes and solutions into place making this transfer more efficient, transparent and more flexible.