Senior Director, Regulatory Affairs
Millipore Sigma
Janmeet Anant, Ph.D., PMP, RAC serves as a Senior Director of Regulatory Affairs at Millipore Sigma, focused on biopharmaceutical manufacturing, specifically working on sterile injectables. Janmeet has been a key member of the Paradigm Change in Manufacturing Operations (PCMO), which is a Quality Risk Management (QRM) team of the Parenteral Drug Association (PDA) focused on continuous improvement and post-approval change management strategies. In addition, Janmeet served as an Executive Board Member for the Bioprocess Systems Alliance (BPSA), Vice-Chair of a subcommittee of the American Society of Mechanical Engineers - Bioprocessing Equipment (ASME-BPE) standard setting organization, and a member of the Regulatory Governance Team at BioPhorum. Janmeet is a key contributor to CMC submission services supporting monoclonal antibody (mAb), viral vector and antibody drug conjugates (ADCs) leading the Contract Testing, Development and Manufacturing Organization (CDMO) regulatory team. With over 25 years of experience in the pharmaceutical industry, Janmeet has been consulting on complex regulatory strategy projects with pharmaceutical drug manufacturers, leveraging skills from his Project Management Professional (PMP) and Regulatory Affairs Certification (RAC). Janmeet has a Bachelor of Science degree in Chemistry and a Ph.D. in Pharmacology.
Tuesday, October 7, 2025
8:30 AM - 4:00 PM EST