19 feb
MEX Solventum Mexico
Ciudad de México
Gracias por tu interés en trabajar para nuestra empresa. Contar con el talento adecuado es crucial para lograr nuestros objetivos. El 01 de abril de 2024, 3M Healthcare experimentó una separación corporativa que condujo a la creación de una nueva empresa denominada Solventum. Aún, estamos en el proceso de actualizar nuestra página de carreras y los documentos de nuestros aplicantes, los cuales actualmente tienen la marca 3M. Mientras tanto, nuestra Política de Privacidad aquí: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ continúa aplicándose a cualquier información personal que envíe, y los puestos de la marca 3M que figuran en nuestra Página de Empleo son para puestos de Solventum.
Igual que con 3M, en Solventum todos los solicitantes calificados serán considerados para un empleo sin importar su raza, color, religión, sexo, orientación sexual, identidad de género, origen nacional, discapacidad o condición de veterano protegido.
Job Description
Regulatory Affairs Specialist, Mexico (Solventum)
3M Health Care is now Solventum
At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.
We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.
The Impact You’ll Make in this Role
As a Regulatory Affairs Specialist you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:
- Providing general regulatory support for Mexico in reference to medical product sold in the country including:
- Managing medical product licenses in Mexico with COFEPRIS
- Reviewing and approving of medical product labeling, claims and advertisements to ensure alignment with country regulations (e.g. NOM-137-SSA1) and COFEPRIS guidances
- Requesting and managing product technical and legal documents from international and regional counterparts as needed for new product registrations or maintenance of current registrations in country
- Compiling, preparing,
and submitting of dossiers for new product registrations/licenses or already established registrations/licenses
- Providing formal and informal assessments of the regulatory pathway for new product introductions or any product changes
- Following business Standard Operating Procedures (SOP’s) regarding specific regulatory activities and tracking with the consultants and distributors
Your Skills and Expertise
To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications
- College Degree in the disciplines of pharmaceutical, chemical, biological, medical, biomedical, biochemical areas or related to Chemistry (BSc) or science career
- Professional License Number and certificate issued
- Written and verbal fluency in both Spanish and English Language
- 5 years of experience in medical product regulatory affairs space,
specifically as it relates to Mexico and COFEPRIS requirements & procedures
Additional qualifications that could help you succeed even further in this role include:
- 7 years of experience in medical product regulatory affairs space, specifically as it relates to Mexico and COFEPRIS requirements & procedures
- Regulatory experience in other Latin America countries (outside of Mexico)
- Experience and knowledge with drug regulations in Mexico
- Advanced knowledge in advertising materials aimed to health professionals under COFEPRIS requirements
- Ability to coordinate multitasks
- Able to anticipate regulatory barriers based on advanced knowledge of medical device regulations and uses challenges as learning opportunities
- Demonstrated ability to collaboratively work with teams to accomplish deliverables
Work location:
· Hybrid/Remote Eligible
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Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with the terms.
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