Cette offre n’est plus disponible.

Chargé(e) Projets Technico-Réglementaire (F/H)

Résumé du poste
CDI
Gentilly
Salaire : Non spécifié
Télétravail non autorisé
Expérience : > 2 ans
Éducation : Bac +5 / Master
Compétences & expertises
Contenu généré
Compétences en communication
Planification et organisation
Aptitude à résoudre les problèmes
Teamwork

BIOCODEX
BIOCODEX

Cette offre vous tente ?

Questions et réponses sur l'offre

Le poste

Descriptif du poste

The position ensures for the HQ all regulatory and monitoring activities of the CMC part (module 3) on a drug portfolio, according to the group strategy and in accordance with the state of the art, the guidelines, and regulations in force. It supports the worldwide objectives of the HQ.

You will join a team of experts working in highly complex projects.

Under the responsibility of the CMC Global Manager, you will work with different departments in Headquarters and our affiliates, in direct connection with our manufacturing plant and our sub-contractors.

With a strong collaboration with the Registrations department, you will :

  • Define strategies for drafting CMC / module 3 documents for new Marketing Authorisation Application (MAA), for variations and renewals files worldwide.
  • Prepare, draft and update module 3 of Marketing Authorisation dossiers and answer CMC questions from the competent Health Authorities.
  • Interact with the Contract Manufacturing Organizations (CMOs) in charge of the manufacturing activities of the drug substances and drug products, including for the activities of process development, for development of analytical methods, etc.
  • Assess the compliance of CMC dossiers by carrying out gap analyses of the documentation in accordance to the group Product Compliance Program and plan associated regulatory strategies to address any identified gaps.
  • Contribute to the development/review of internal standard procedures related to CMC activities.
  • Provide scientific and technical monitoring of projects.

You will also participate in quality activities (change controls, deviations, audits, CAPA).


Profil recherché

Profile :

  • Pharmacist Doctor or Master in Science or Engineering.
  • Minimum 3 years relevant / CMC experience is required.
  • Knowledge and understanding of the CMC and regulatory environment is required.
  • CMC Experience with biological products would be a plus.

Functional and Technical Competencies :

  • Strong analytical and problem-solving skills.
  • You can work in project mode, you have a sense of teamwork and ability to act as liaison with other departments where necessary.
  • Excellent organizational and planning skills.
  • Strong verbal and written communication skills in English, working in an international environment;
  • Excellent interpersonal skills, relationship building skills.

Our four values are driving forces and bonds for all teams: we play collectively; we shape fair relations; we dare to innovate; we care for our ecosystem.

We cherish diversity in our teams and we want to build inclusive workplaces.

At Biocodex, our CSR approach is an holistic one to reconcile the « 4P's »: « People, Planet, Profit and Purpose ». Join us !

Envie d’en savoir plus ?

D’autres offres vous correspondent !

Ces entreprises recrutent aussi au poste de “Conseil en conformité réglementaire”.