QbDVision Appoints Former Takeda Executive Christoph Pistek as VP of Digital CMC Solutions

13 November 2026 | Friday | News

Pistek brings more than 20 years of pharmaceutical industry experience, including leadership roles at Takeda. He will support QbDVision’s customers in modernising chemistry, manufacturing and controls (CMC) processes through digital technology, structured data and automation to improve drug development and manufacturing efficiency
Image Source: Public Domain

Image Source: Public Domain

QbDVision, a provider of a Digital CMC platform for pharmaceutical and biotechnology companies, has announced the appointment of Christoph Pistek as Vice President, Digital CMC Solutions. Pistek will help customers start their CMC transformation, taking them from their original business objective through to technology implementation.

Pistek joins from Takeda, where he led global innovation initiatives as VP and Head of Sustainability and Technology in Pharmaceutical Sciences. He brings over 20 years of experience across R&D, technical and supply operations, and business excellence, with a track record in digital and organizational transformation.

Commenting on the appointment, Yash Sabharwal, CEO and Co-founder of QbDVision, said: “Christoph has implemented Digital CMC at scale from inside a global pharma company. He understands why transformation stalls and how to move it forward, and our customers will benefit from that experience.”

Digital CMC brings therapies to patients faster by speeding up drug development and technology transfer, replacing manual, paper-based workflows with structured data and automation. It can also help address a broader range of unmet medical needs, including diseases that have historically attracted less investment.

“Too often, digital transformation in CMC is run as a technology project,” Pistek said. “The organizations that get real value start from the business objective and own the transformation at the highest level.”

He continues: “CMC depends on input from more functions than almost any other part of a drug developer, for example, research, manufacturing, quality, regulatory, and commercial. We frequently see organizations lose valuable time to repeated assessments and RFPs, while costs climb and the status quo is locked in. The real risk isn’t getting it wrong; it's doing nothing, and continuing to work within the constraints of slow, manual, unstructured processes.”

 

Survey Box

Poll of the Week

Which area of biopharmaceutical research excites you the most?

× Please select an option to participate in the poll.
Processing...
× You have successfully cast your vote.
 {{ optionDetail.option }}  {{ optionDetail.percentage }}%
 {{ optionDetail.percentage }}% Complete
More polls
Stay Connected

Sign up to our free newsletter and get the latest news sent direct to your inbox

© 2026 Biopharma Boardroom. All Rights Reserved.

Show

Forgot your password?

Show

Show

Lost your password? Please enter your email address. You will receive a link to create a new password.

Back to log-in

Close