lourdes torres

senior specialist regulatory cmc

About

Technical regulatory affairs specialist Specialties: Pharmaceutical products

Country

switzerland

City

lausanne

Industry

pharmaceuticals

Skill

regulatory affairs, pharmaceuticals, pharmaceutical industry, pharmacovigilance, gmp, regulatory submissions, cmc, regulatory requirements, ectd, regulations, pharmaceutics, drug development, clinical development, change control, sop, fda, 21 cfr part 11, clinical trials

Experience

global regulatory affairs, cmc specialist

novartis

2010-12 - 2012-8 · 1 yr 9 mos

international technical regulatory project leader

bayer healthcare

2007-11 - 2010-11 · 3 yrs 1 mo

third party technical regulatory project leader

bayer healthcare

2006-6 - 2007-9 · 1 yr 4 mos

global regulatory affairs, cmc senior specialist

novartis

2012-9 - Present · 14 yrs 1 mo

senior specialist regulatory cmc

merck group

2016-3 - Present · 10 yrs 7 mos

Not intended for US & CA visitors. Merck is a leading science and technology company in healthcare, life science and performance materials. Around 50,000 employees in 66 countries work to further develop technologies that improve and enhance life – from biopharmaceutical therapies to treat cancer or multiple sclerosis, cutting-edge systems for scientific research and production, to liquid crystals for smartphones and LCD televisions. Your possibilities to develop in our growing company are just as manifold as our product portfolio. We offer a modern and international working environment to unleash your innovative potential in diverse teams, and take responsibility for our employees, products, the environment and society. Sound like something you'd like to be part of? Explore come2merck.com to see how we can help you make great things happen.