5 jobs found for biotechnology / pharmaceuticals

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Specialist in Submission Publishing who will be responsible for executing the electronic publishing of complex regulatory submissions for national, regional and global regulatory agencies and operating companies in both eCTD and non-eCTD format. If you have relevant experience and would like to participate in the process, apply for this role.what

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Senior / Specialist in Submission Publishing who will be responsible for executing the electronic publishing of complex regulatory submissions for national, regional and global regulatory agencies and operating companies in both eCTD and non-eCTD format. If you have relevant experience and would like to participate in the process, apply for this r

For our Client, one of the largest Pharmaceutical companies worldwide, we are looking for Global Labeling  Senior Associate , who will ensure quality of primary and derived labeling documents and ensure support for the documents.If you have relavant experience and would like to participate in the global labeling strategy, apply for this role.what we offerBeneficial leave policiesMedical Care program & Life InsurancePension planReimbursement of Exercises/We

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Manager EMEA  , who will provide regulatory support to the Portfolio Leader for a portfolio of marketed oncology and internal medicine drug products which are supported by the Established Products team.If you have relevant experience and would like to participate in the process, apply for this role.what we offerannual performance-based bonusopport

For our Client, one of the largest Pharmaceutical companies worldwide, we are looking for Regulatory Affairs Mananger / Senior Manager in Global Labeling, who will ensure quality of primary and derived labeling documents and ensure support for the documents.If you have relavant experience and would like to participate in the global labeling strategy, apply for this role.what we offerBeneficial leave policies Medical Care program & Life Insurance Pension pl