Regulatory Affairs - Product Variations

CMC, regulatory, rejestracja
Your responsibilities:
  • Managing multiple CMC (Chemistry, Manufacturing and Control) Variations and source transfers for Finished Products and Active Pharmaceutical Ingredients for Pharma and Vaccines products
  • Managing routine assigned projects: define and agree regulatory strategy, complete data assessment to ensure authored regulatory dossier is in compliance with company regulatory processes and external requirements for local markets e.g. Europe (for Centralised, Mutual Recognition and Decentralised procedure submissions), US and International countries
  • Working with colleagues in Global Manufacturing & Supply, Global Regulatory Groups and Local Operating Companies in markets worldwide to deliver high quality dossiers on time
  • Building and maintaining good relationships with internal and external stakeholders
  • Monitoring regulatory intelligence and acting proactively on identified changes to the regulatory requirements
  • Identifying the improvement opportunities for CMC Regulatory processes, policies and systems
Our requirements
  • Relevant experience in regulatory affairs, pharmaceutical industry (familiarity with post-approval CMC regulatory procedures and ICH CTD documentation)
  • Bachelor’s or Master's degree in biotechnology, chemical technology, pharmacy, chemistry or other related science or technical field
  • Understanding of the pharmaceutical industry, drug development environment, and regulatory processes.
  • Attention to detail with emphasis on accuracy and completeness
  • Ability to handle multiple tasks, to meet constantly shifting priorities and to schedule work to meet business needs,
  • Flexible and analytical thinking to independently provide solutions to issues,
  • Excellent interpersonal skills; ability to communicate clearly and effectively, work in a diverse team environment and build relationships across a large organization.
  • Excellent written and verbal communication skills in English and Polish
What we offer
  • Remote work (during pandemic)
  • After Pandemic - Performance with Choice – flexibility in working mode (hybrid between office and remote work based on employee needs)
  • Established job in an international, well-known pharmaceutical company
  • Opportunity to work in professional team playing crucial role in introducing company portfolio to the market
  • Opportunity to work within company standards and documentation applied globally
  • Wide range of benefits (Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus)
  • Canteen for employees at site (with discounts)
  • Flexible working hours
Kliknij tutaj aby uzyskać dostęp do Polityki prywatności HAYS, która zawiera szczegółowe informacje na temat tego, w jaki sposób wykorzystujemy i chronimy twoje dane osobowe oraz Twoje prawa z tym związane.


Rodzaj pracy
Obszar specjalizacji
Nr ref.:
Data ważności
31 May 2022

Skontaktuj się z konsultantem

Skontaktuj się Aleksandra Figielska, Konsultant odpowiedzialny za tę rekrutację, znajduje się Warszawa
Hays, ul. Marszałkowska 126/134

Telefon: 722000702