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Regulatory Affairs Specialist / Manager (f/m/d) 80%-100%

Verfora

Employment type
Full-time
Workload
80–100%
Location
Villars-sur-Glâne · Remote possible
Languages
German, German
First posted
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Regulatory Affairs Specialist / Manager (f/m/d) 80%-100% #

  • Villars-sur-Glâne and Worb
  • Verfora AG
  • Espace Mittelland (BE, FR, NE, JU, SO)
  • Quality Management / Regulatory Affairs

Do you want to make a difference in the pharmaceutical sector and help shape the availability of safe, effective and regulatorily compliant health products? You will take responsibility for a versatile portfolio throughout the entire product lifecycle.

What you can achieve ##

  • You ensure the regulatory compliance of your portfolio of medicinal products, dietary supplements and medical devices from development to the end of the product lifecycle
  • You create, write and submit regulatory documentation and keep dossiers as well as product labeling up to date according to current requirements
  • You develop project-specific submission strategies and coordinate these directly with authorities and partners in Switzerland and internationally
  • You support development teams at an early stage, recognize regulatory requirements and risks and derive viable options for action from them
  • You work closely with Quality, R&D, Marketing and Medical Affairs and bring your regulatory perspective into portfolio decisions
  • You follow regulatory and scientific developments, particularly in the pharmaceutical sector as well as, depending on the portfolio, in herbal medicinal products and phytotherapy

What you bring with you ##

  • You have a university degree in pharmacy, chemistry, biology, biomedical sciences or a comparable scientific field
  • You have very good professional German and French skills in speaking and writing and can work independently in both languages
  • You have good English skills for scientific and regulatory documentation as well as for exchange with international partners
  • You analyze complex scientific and regulatory issues precisely and represent your position clearly to internal teams, partners and authorities
  • You reliably organize multiple priorities, recognize challenges early and develop pragmatic solutions
  • You have a particular affinity for herbal medicinal products, plant substances or phytotherapy; experience in this area is an advantage
  • Ideally, you bring around two years of experience in Regulatory Affairs in the pharmaceutical industry

You will work at the locations Villars-sur-Glâne (main place of work) and Worb in a hybrid working model with home office.

What we offer you ##

5 weeks of vacation, with the possibility to purchase up to 10 additional vacation days or take unpaid leave

Pension fund with advantageous premium distribution - approx. 2/3 are covered by us

Various discounts in our pharmacies and with other top brands

Expand competencies through promoted and supported training and further education as well as internal development opportunities

Family-friendly with 16 weeks of maternity leave (100% of salary) and 20 days of paternity leave (100% of salary), as well as participation in a child fund

Registered shares at preferential prices - not only commit to Galenica professionally, but also invest

Mobile and flexible working in consultation with the team

Learn more about the benefits

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Posted 2 weeks ago

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