Regulatory Affairs Specialist

hace 6 días


Barcelona, Barcelona, España COCUNAT A tiempo completo
About the Role

COCUNAT is seeking a highly skilled Regulatory Affairs Specialist to join our R&D team in Barcelona. As a key member of our team, you will be responsible for ensuring compliance with EU and international regulations for our cosmetics products.

Key Responsibilities
  • Prepare and maintain documentation for product registration in European markets.
  • Ensure compliance with EU and international regulations for raw materials and finished products.
  • Manage internal and external documentation, including classification and digital filing.
  • Support the quality department in managing incidents and reviewing CoAs.
  • Review and adapt legal texts for labeling and promotional materials.
  • Prepare technical and safety data sheets.
  • Manage legal procedures with official health organizations.
  • Provide back-office support to the R&D department.
Requirements
  • Degree in Chemistry, Biology, or Pharmacy.
  • Master's in Cosmetology and Dermocosmetics.
  • Minimum of 3 years of experience in a similar position in the cosmetics industry.
  • Knowledge of EU, USA, and Mexico regulations.
  • Experience interacting with research and marketing teams.
  • Strong analytical skills and attention to detail.
  • Native Spanish speaker, high proficiency in English.
Why COCUNAT?

COCUNAT is a digital native cosmetics brand with a strong presence in Europe and the United States. We are committed to creating sustainable and safe products for our customers. As a Regulatory Affairs Specialist, you will be part of a dynamic and open environment where you can make a real difference.

About Us

COCUNAT is a young startup with a strong focus on innovation and sustainability. We are committed to creating a positive and inspiring movement that makes people aware of the importance of sustainable and safe cosmetics. Join us in our mission to create a healthier, more sustainable, and safer cosmetics industry.



  • Barcelona, Barcelona, España Galderma Pharma S.A A tiempo completo

    Job Title:Regulatory Affairs SpecialistGalderma Pharma S.A is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The ideal candidate will have a strong...


  • Barcelona, Barcelona, España Ramboll Group AS A tiempo completo

    Regulatory Affairs SpecialistAt Ramboll Group A/S, we are seeking a highly skilled Regulatory Affairs Specialist to join our international Health Sciences service line. As a key member of our team, you will be responsible for providing technical support to clients and colleagues on issues relating to product regulatory compliance and stewardship in Spain.Key...


  • Barcelona, Barcelona, España Alk-Abelló AS A tiempo completo

    Job Title: Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Alk-Abelló A/S. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with regulatory requirements and ensuring the smooth submission of CMC documentation for Marketing Authorisation...


  • Barcelona, Barcelona, España Grifols A tiempo completo

    Join Grifols as a Regulatory Affairs SpecialistWe are committed to fostering an inclusive environment and promoting diversity in our business, teams, and culture. As a world leader in plasma-derived medicines, we need a skilled Regulatory Affairs Specialist to help us lead the way.Your Key Responsibilities:Prepare and submit technical documentation for...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategiesAssess regulatory impact...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategiesAssess regulatory impact...


  • Barcelona, Barcelona, España Algaktiv A tiempo completo

    Regulatory Affairs SpecialistAlgaktiv is a biotechnology and microalgae specialist company headquartered in Barcelona, Spain, working with skincare brands to create unique formulations using high-performance active ingredients. We are seeking a highly skilled and motivated Regulatory Affairs Specialist to join our team.Key ResponsibilitiesEnsure compliance...


  • Barcelona, Barcelona, España Algaktiv A tiempo completo

    Regulatory Affairs SpecialistAlgaktiv is a biotechnology and microalgae specialist company headquartered in Barcelona, Spain, working with skincare brands to create unique formulations using high-performance active ingredients. We are seeking a highly skilled and motivated Regulatory Affairs Specialist to join our team.Key ResponsibilitiesEnsure compliance...


  • Barcelona, Barcelona, España Grifols A tiempo completo

    Join Our Team as a Regulatory Affairs SpecialistWe are committed to fostering an inclusive environment and promoting diversity within our organization. As a Regulatory Affairs Specialist, you will play a crucial role in ensuring compliance with regulatory requirements and facilitating the registration and renewal of our products.Key Responsibilities:Prepare...


  • Barcelona, Barcelona, España Grifols A tiempo completo

    Join Our Team as a Regulatory Affairs SpecialistWe are committed to fostering an inclusive environment and promoting diversity within our organization. As a Regulatory Affairs Specialist, you will play a crucial role in ensuring compliance with regulatory requirements and facilitating the registration and renewal of our products.Key Responsibilities:Prepare...


  • Barcelona, Barcelona, España Grifols A tiempo completo

    Job Title: Packaging Regulatory Affairs SpecialistWe are seeking a highly skilled Packaging Regulatory Affairs Specialist to join our Biopharma Regulatory department at Grifols.Key Responsibilities:Prepare, review, and follow up on documentation generated at the Regulatory Affairs department or needed for a regulatory submission, ensuring timeliness,...


  • Barcelona, Barcelona, España Grifols A tiempo completo

    Job Title: Packaging Regulatory Affairs SpecialistWe are seeking a highly skilled Packaging Regulatory Affairs Specialist to join our Biopharma Regulatory department at Grifols.Key Responsibilities:Prepare, review, and follow up on documentation generated at the Regulatory Affairs department or needed for a regulatory submission, ensuring timeliness,...


  • Barcelona, Barcelona, España Bitfinex A tiempo completo

    Regulatory Affairs SpecialistBitfinex is seeking a highly skilled Regulatory Affairs Specialist to join our Regulatory and Licensing team. The successful candidate will have a deep understanding of legal and regulatory requirements pertaining to the crypto-asset industry in the Middle East / North Africa region.Key Responsibilities:Develop and execute...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Job Title: Regulatory Affairs SpecialistGalderma is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.Develop and manage clinical trial regulatory...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Job Title: Regulatory Affairs SpecialistAt Galderma, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities. You will work closely with our global...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Job Title: Regulatory Affairs CMC SpecialistGalderma is seeking a highly skilled Regulatory Affairs CMC Specialist to join our team. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategies and assess...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Job Title: Regulatory Affairs CMC SpecialistGalderma is seeking a highly skilled Regulatory Affairs CMC Specialist to join our team. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategies and assess...


  • Barcelona, Barcelona, España Alk-Abelló AS A tiempo completo

    Job Title: Regulatory Affairs SpecialistJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Alk-Abelló A/S. As a Regulatory Affairs Specialist, you will be responsible for handling regulatory CMC documentation of products manufactured at our site in Madrid, for worldwide submissions. You will also be responsible for...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Job Title: Regulatory Affairs CMC SpecialistWe are seeking a highly skilled Regulatory Affairs CMC Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating the CMC (Chemistry, Manufacturing and Control) dossier sections of assigned products.Key...


  • Barcelona, Barcelona, España Galderma A tiempo completo

    Job Title: Regulatory Affairs CMC SpecialistWe are seeking a highly skilled Regulatory Affairs CMC Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating the CMC (Chemistry, Manufacturing and Control) dossier sections of assigned products.Key...