reklama
Praca regulatory affairs specialist, Polska
Mamy dla Ciebie 30 ofert-
- 2 lokalizacji
Your responsibilities, Manage routine assigned projects, analyze regulatory strategy with your own input, provide comprehensive data assessment to ensure authored regulatory dossier is in compliance with GlaxoSmithKline regulatory processes and...opublikowana: 23 lutego 2021 -
- 2 lokalizacji
Your responsibilities, Managing Market Specific Requirements for Finished Products and Active Pharmaceutical Ingredients in various areas, Complete data assessment to ensure authored regulatory dossier is in compliance with GlaxoSmithKline...opublikowana: 23 lutego 2021 -
- 2 lokalizacji
Key Responsibilities: Managing multiple CMC (Chemistry, Manufacturing and Control) Variations assignments for Finished Products and Active Pharmaceutical Ingredients Define and agree strategy, complete data assessment to ensure authored...opublikowana: 22 lutego 2021 -
- Warszawa
Your responsibilities, Handling matters related to the maintenance of marketing authorizations for medicinal products in Poland., Preparation of registration documentation in a correct manner and in accordance with applicable regulations and...opublikowana: 22 lutego 2021 -
- Szczecin
Would you like to work with products that actually change the lives of people worldwide and do it in a fast-growing company? Then we can offer you the right challenge! Right now, we are looking for a dedicated and skilled Regulatory Affairs...opublikowana: 21 lutego 2021 -
- 16 lokalizacji
What you’ll learn & achieve: You will be in charge of the CE certification management (e.g. processing certifications in our system, making changes, performing evaluations, etc.) You will collaborate closely with internal and external...opublikowana: 19 lutego 2021 -
- Wrocław
Job ID: EMEA01268 Location: Wrocław Department: QA / QC / Regulatory Affairs Employment Type: Regular Full-Time Position Description Prepare, compile and complete submissions to global regulatory entities for QIAGEN’s In vitro Diagnostic and...opublikowana: 19 lutego 2021 -
- 2 lokalizacji
Na co dzień będziesz zajmować się: Przygotowaniem dokumentacji rejestracyjnej Prowadzeniem procedur rejestracyjnych (dopuszczenia do obrotu, re-rejestracji, zmian porejestracyjnych, notyfikacji) Współpracą z zagranicznymi przedstawicielami i...opublikowana: 17 lutego 2021 -
- Warszawa
KEY RESPONSIBILITIES In your new role you will: take responsibility for planning, preparation, technical review, delivery and associated regulatory activities of CMC Annual Reports (for NDAs/BLAs/DMFs/DSURs and Brazil ARs), Site Registrations and...opublikowana: 17 lutego 2021 -
- Warszawa
Responsibilities: working closely with regional, country, global cross-functional teams, communicating and executes regulatory strategies and plans, supporting the development of country/regional positions on regulatory risk-benefit, supporting...opublikowana: 16 lutego 2021
