Our Team

Industry Veterans. Strategic Thinkers. Trusted Advisors.

At CheMaC, our team is composed of seasoned professionals with decades of experience across the pharmaceutical value chain. We bring together specialists in process chemistry, analytical development, regulatory affairs, GMP manufacturing, quality systems, EHS, and CMC project management, all with proven track records in top global and Indian pharma/CDMO organizations.

What Sets Our Team Apart

Collective Expertise

Over 200+ years of combined experience in drug development, regulatory submissions (IND, NDA), commercial manufacturing support and other associated pharmaceuticals disciplines.

Global & Local Insight

Deep understanding of both international regulatory frameworks (FDA, EMA, MHRA, PMDA etc) and India’s cost-effective manufacturing landscape.

Hands-On Approach

Our consultants are not just advisors—we actively engage on-site, driving project success through direct oversight and collaboration.

Client-Centric Mindset

Every team member is focused on tailoring solutions to meet each client's unique technical, operational, and regulatory needs.

Collaborative Network

We leverage a strong professional network across CDMOs, CROs, raw material suppliers, and regulatory bodies to accelerate outcomes.

Meet The Minds Behind The Mission

Process R&D

expert with 24 years of experience from different cultural environments (USA, UK & India) and worked in leading CDMO’s

20+ years in Regulatory Affairs

“Led multiple CMC filings for successful NDA approvals across US and EU.”

Former Head of Manufacturing

“Oversaw tech transfers of several products at global CDMO facilities.”

Ex-QA Director

“Managed 20+ successful audits including FDA, EMA, and MHRA.”

Senior EHS Consultant- An industry veteran

“Implemented sustainability and safety systems in multiple GMP plants.”

Competitive Edge

Our competitive edge lies in deep industry expertise, agile execution, and customized CMC solutions for every client.

#Robust Network of CDMO Partners

We leverage our deep industry connections to help clients identify, select, and oversee the most suitable CDMOs for their manufacturing needs.

#Global Compliance Focus

We align with the latest FDA, EMA, and ICH guidelines, ensuring seamless approvals and regulatory success for your project

#On-Site Project Oversight

We physically monitor projects at CDMO sites (unlike remote-only consultants), ensuring higher efficiency and faster problem resolution.

#End-to-End CMC Expertise

Our team provides comprehensive services & solutions across process development& manufacturing, analytical method development & validation, regulatory strategy, quality compliance, and supply chain management.

#Professionals-Led Expertise

Unlike other consulting firms, CheMaC Life Sciences is founded by industry veterans with strong experience in CRDMO business operations. Our in-depth knowledge gives us a strategic advantage in CMC services tailored to your requirement.