Timothy Reinhardt

Timothy Reinhardt is a highly experienced professional with more than twenty-four years in the pharmaceutical and medical device industry. His expertise includes leadership, quality management, process improvement, technical knowledge, problem-solving, and planning/scheduling skills.

Timothy's pharma background spans investigational material and commercial organizations, including outsourcing facilities in multiple regions such as the U.S., Puerto Rico, Asia, and Europe. He has extensive experience in pharmaceutical materials, systems, regulations, and various dosage forms.

In addition to pharmaceuticals, Timothy has knowledge in Active Pharmaceutical Ingredients (API), gene therapy, and medical devices. He has conducted GMP, GLP, and GCP compliance assessments globally and is known for his strong communication, interpersonal, organizational, and leadership skills.

Timothy Reinhardt pursued education at reputable institutions including San Francisco State University, University of California, Davis, and Stevens Institute of Technology. His academic background complements his practical industry experience.

Throughout his career, Timothy has held significant roles such as Sr. Consultant/Site Manager at RMC Pharmaceutical Solutions, Director/Team Leader at Pfizer, Sr. Manager - MSQA at Pfizer, and QA positions at Amylin Pharmaceuticals and Alza. He has also showcased his writing talents at Sid Lives Productions.

With a proven track record in pharmaceutical and medical device sectors, Timothy Reinhardt stands out as a seasoned professional with a diverse skill set and a deep understanding of industry regulations and operations.