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Robert Potts is Director, International Quality at Vertex Pharmaceuticals for 9 + years. There he is responsible for the international expansion and product distribution internationally. He has over 14 years experience in the pharmaceutical industry. He has founded knowledge in GDP, GMP, GCP, GPVP. Read more

Dedicated, dependable and motivated professional with over 10+ years of experience in Quality Assurance, Quality Control, Training & Development, Pharmacovigilance processes and Regulatory compliance & audits and Medical device sector. Proficient in initiating, investigating, root cause analysis and closure of market complaints within stipulated timelines. Skilled in documentation, verification and approval of Standard Operating ProcedureRead more

Seasoned professional with 11+ years of work experience in a wide variety of roles spanning from MSAT, Life Cycle Management, Strategy, Process Development, Design Engineering and Cell Therapy Research. Passionate to lead and engage my interdisciplinary skills towards acceleration and delivery of novel therapeutics to patients in need globally.Read more

Reliability Engineer at Eli Lilly – Significant work spent on Failure Analysis, Process Optimization, Instrumentation Calibration, and Maximo Programming. Outside of work, I enjoy hiking and backcountry camping, diving into a good book, and cherishing quality time with family and friends!Read more

With over 20 years’ experience in life sciences and biopharma, Chad Gerald is a proven leader with a comprehensive engineering, maintenance and reliability background. As a Maintenance and Reliability Lead, he is accountable for manufacturing and laboratory equipment performance for multiple cGMP manufacturing and warehousing sites. Throughout his career, he’s held a passion for mentoringRead more

Mai Ly has been with we.CONECT Global Leaders GmbH since 2024. With a Bachelor of Business Administration (BBA) and a background in sales and communications, she has developed skills in understanding customer needs, supporting product improvements, and enhancing team communication. Her various roles have allowed her to grow these abilities and reflect her passion forRead more

Tina Self serves as the global lead for the Biologics Manufacturing Capability Cluster, responsible for clinical through commercial manufacturing of Bayer’s biologics portfolio. She also serves as the Site Head for Bayer’s biotech campus in Berkeley, California. Prior to taking on this role in June 2024, she has advanced through positions of increasing responsibility inRead more

With over 20 years of experience in industrial process improvement, Christophe Rondeau has developed expertise in managing key phases of continuous improvement, with a strong focus on optimizing production flows, ensuring optimal safety conditions, and structuring efficient maintenance departments. His work is centered around driving operational excellence through practical solutions that enhance safety, streamline processes,Read more

Brian DiVasta is Director for Computer System Validation for ElevateBio for 4+ years. There his specialties are computer validation and quality assurance. Before his position at ElevateBio he was with Sanofi for 8+ years as Associate Director, ITS Compliance.Read more

Professional in the Pharmaceutical Industry with a 23-year career experience distinguished by performance, self-starter and organization. Strong 23 years background in Maintenance Organization, including direct experience in Manufacturing & Packaging Maintenance, Utilities, Spare Parts, Pest Control and Instrumentation/Calibrations Management and Improvement, focused on Customer Service. Expert in maintenance and calibration maintenance systems (RAM, MAXIMO, SAP,Read more