We are growing, grow with us

Want to work in a dynamic company with daily new challenges and opportunities?  Then is PharmaLex your career opportunity.
PharmaLex is one of the leading service companies for the global pharmaceutical industry and specializes in all aspects of drugs and medical devices approval of the development to market and any action to product maintenance make it as effective as possible.
The success of our company grows with the excellent expertise and the high motivation of our employees.
If for you, your profession is not only a job but a mission too and you enjoy working with people, then you are welcomed to come and join us.
To strengthen our successful team, we are looking, as earliest as possible for a:

Specialist Regulatory Affairs

Your Job

  • Operates as a member of the CMC product team to provide project management support for development and maintenance of timelines and collection of CMC deliverables related to preparation m3 and 2.3 documentation, for new product registrations or post-approval changes including annual reports, registration renewals, supplements, variations, commitments, tender bids and responses. Provision of support for other CMC projects and activities, as required

We offer you

  • Diversified and challenging job
  • Open and collaborative organisational culture with emphasis on knowledge-sharing
  • Flexible working hours based on trust
  • Continuous development opportunities through knowledge and experience as well as training

Your Profile

  • Preferably degree in natural sciences (chemistry, biology, pharmacy) 
  • Prior regulatory affairs, quality control and quality assurance experience is a plus
  • Distinctly strong service orientation
  • Independent approach to work, flexibility and dedication
  • Fluency in English, spoken and written (C1 -advanced-, might be considered an advantage)
  • Strong sense of responsibility, organizational skills and intrinsic motivation