Job DescriptionGlobal Regulatory Affairs Labelling Consultant/SME - International Submissions - 6 month Contract
If you are looking to work for an established Biotech company that is continuously investing to grow even further and which will make your profile more attractive for future clients, then look no further.
Due to my client's growth and new product introduction in several markets they are looking for a Regulatory Affairs professional in Labelling to help with the extra workload.
You will be covering the European market as a Subject Matter Expert related to product labeling for new drug applications as well as licensed products for the assigned Region.
The perfect regulatory affairs candidate needs to have a minimum of 5 years experience in a Global Regulatory Affairs function with knowledge of regulatory product labeling and related processes together with being capable in interacting at a higher level with the other departments in the company.
The contract will be 6 months with a partial flexibility in home office, however when needed the consultant needs to be present in either my client's office in Germany or Switzerland, we are looking at an Immediate Start Date is posible.
Experience in within the EU is needed. Please note we can only accept applications from candidates who hold valid European Union passport and are able to work in Europe without visa sponsorship.
For a confidential discussion about quality assurance and technical roles, then send your CV to firstname.lastname@example.org, Elena Cazacu, Senior Recruitment Consultant for Switzerland.