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Regulatory Affairs Manager

Synthorx

Synthorx

Legal
Budapest, Hungary
Posted on Wednesday, May 8, 2024

Regulatory Non Drug Manager - Sanofi - Budapest

Regulatory Non Drug Manager

The Regulatory Non Drug Manager (RNDM) supports the regulatory compliance for marketed products by means of a correct handling of all regulatory activities for the product portfolio under the RNDM’s responsibility. This included the support of product license’s maintenance and site registration.

The RNDM evaluates the compliance of new products (in-licensing project and development projects) with both the regulations in force and with the internal requirements.

The RNDM Ensures the role of regulatory expert for all regulatory topics and projects for the assigned CMO’s.

Duties

• Prepares the technical dossiers for registrations in collaboration with GRA teams and external partners and ensure data entry in regulatory database for :

  • Initial registration
  • Site registration
  • Territory extension
  • Variation
  • Renewal
  • Responses to authorities
  • Ensures the compliance of the Non Drug products (Medical Devices, Nutraceuticals and Cosmetics) according to the applicable regulations and the Sanofi quality requirements for development projects and marketed products.
  • Contributes to the Due diligences for in-licensing projects and to the preparation of the launch for new development project for all regulatory aspects.
  • Ensures the change control management in the appropriate tool and evaluates Change Control with regulatory impact in collaboration with GRA and /or Affiliates Regulatory focal point.
  • Ensures the regulatory intelligence and develops the team expertise and evaluates the impact on the portfolio under RNDM responsibility in the case of any new regulations and guidance.
  • Ensures the review of the regulatory part of the Product quality review if applicable.
  • Coordinates the regulatory interface with Global Regulatory Affairs or with Affiliate Regulatory Affairs and CMOs.
  • Contribute to KPIs reporting for activities under his/her responsibility
  • Supports the Quality team, Innovation team, Supply Chain team and Transfer team for all regulatory aspects.
  • Collaborates with Quality System team and IA CHC for establishing internal procedures and new Ways of Working for Non Drug products.
  • Contributes to site inspections, audits and Site Quality review as appropriate

Background and experiences :

  • Advanced Degree (Master) in a science/health field (e.g., Chemistry, Pharmacy, Biological/Biotechnology Sciences etc.), or equivalent
  • Experience in Regulatory Affairs or any relevant experience in Medical Devices, Food Supplements and/or Cosmetics.
  • Should have broad knowledge of global regulations/guidelines on Medical Devices, Food supplements and/or cosmetics.
  • Should demonstrate flexibility, proactivity and be able to communicate efficiently with various stakeholders internally and externally.
  • Should demonstrate solid oral communication and writing skills in an international environment.
  • Fluent in English.

When joining our team, you will experience:

  • An international work environment, in which you can develop your talent and realize ideas and innovations within a competent team
  • An attractive, market-oriented salary and cafeteria benefits
  • Flexible home office policy, with a possibility to work up to 60% of time from home / where you can easily schedule your office days
  • Work from an "Office of the Year 2020" finalist office
  • Collective life and accident insurance
  • Yearly medical check-up
  • An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
  • Your own career path within Sanofi. Your professional and personal development will be supported purposefully
  • Practice your language skills within our "Language Club"
  • Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability, gender identity or Veteran status.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

#Sanofi #WeNeverSettle

#SanofiCareers

#PursueProgress

#DiscoverExtraordinary

#joinsanofi

#careerswithpurpose

#SBSBUDAPEST

#LI-CHC

#LI-EUR

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!