Since the start in 2006, Svensk Medicin AB has successfully coached 2 500 individuals to new jobs and trained over 2 000 clients in different courses. Over 1 500 people has been certified and gained confidence by competence.
With a vast network and documented success, we are confident that we will be able to help You to a new career, new job, new certified competences and a brand new title.
clients to new jobs
clients in courses
seminars & courses
Lecturer- Medical Affairs - CEO
Owner and CEO of Svensk Medicin AB. A senior level Scandinavian - Global Career Developer, Scientific marketeer, scientific advisor and dynamic product- and marketing specialist, qualified to practice in all areas of different therapeutic sectors. Over 25 years of experience of new launches, re-launches and documented success for several top key products among the 10 largest pharmaceutical companies in the world. Solid established network of top key decision makers in national and international recruitment.
Lecturer - Regulatory Affairs & GDP
Strategic and business driven senior leader. Experience from big Global as well as small Swedish companies. Used to leading companies through changes, acquisitions and mergers.
Strengths within Regulatory, Quality and Pharmacovigilance, and late phase development together with launch preparations of pharmaceuticals.
Lecturer - GMP
After completing his Ph.D. in organic chemistry, Roberto has 27 years of professional experience.
That includes 25 years within the pharmaceutical industry and some years in the food/beverage sector. He has worked as a researcher, developer, project manager, trainer, production engineer and as a line manager. Roberto has experience working in both Swedish and global multinational companies, ranging from small companies to large ones. As a certified an appreciated GMP lecturer he brings experience and many examples from several different companies from his roles in different industries. He has experience from all sectors that rules under GMP.
Lecturer - Pharmacovigilance
As a seasoned pharmacovigilance trainer with 12 years of hands-on experience, she has a wealth of knowledge in end-to-end PV systems, including ICSR case management, regulatory reporting, and signal detection. With over a decade of experience, she has a proven track record in writing, reviewing, and approving aggregate reports, risk management plans, and performing literature searches.
Her skills and extensive knowledge of PV makes her a valuable asset in training professionals to understand and implement effective PV practices. She is confident in her ability to create and deliver training programs that will help professionals develop their skills and succeed in their PV roles.