Brazil Job Openings
Sanofi US
Regulatory Senior Analyst
São Paulo
October 21, 2024
Principais Responsabilidades
- Collaborate with Global Functions, R&D, Quality Assurance, Marketing, and other departments to ensure regulatory requirements are considered in product development and post-market activities;
- Provide regulatory guidance to support changes to existing products;
- Assist in the preparation and submission of regulatory documents to Health Authorities;
- Track and manage submission timelines to ensure timely approvals and escalate any possible risk to local and global teams;
- Work collaboratively with relevant stakeholders to identify solutions and mitigate potential impacts on timelines or project objectives;
- Implement a comprehensive regulatory strategy that aligns with project objectives and local regulatory requirements, considering timelines, risks, and potential challenges;
- Participate in the evaluation of promotional materials, ensuring they comply with current legislation and internal procedures;
- Update the company's systems and databases;
- Manage the artwork approval process through the internal system;
- Establish and maintain positive relationships with regulatory authorities in Brazil;
- Act as a point of contact with regulatory agencies, responding to inquiries and requests for additional information;
- Contribute to influencing regulatory bodies and health authorities by actively participating in meetings/committees and building relationships to review and update legislation, assess business impacts, and provide clarifications on projects and products;
- Promote compliance with internal processes, metrics, and controls, focusing on portfolio registrations and their maintenance.
Colaboradores individuais
Sobre você
-
Bachelor’s degree in Pharmacy, Life Sciences, or a related field.
-
Minimum experience of 3 years in Regulatory Affairs, preferably within the pharmaceutical industry.
-
Proven experience in LCM and dossier preparation for regulatory submissions.
-
Strong knowledge of regulatory frameworks and requirements in Brazil;
-
Ability to work collaboratively with cross-functional teams, including R&D, Marketing, Quality, and other departments.
-
Excellent organizational skills with the ability to manage multiple projects and timelines simultaneously.
-
Fluent English is required.
Persiga o progresso, de scubra o extraordinário
-
Sempre visando a segurança e bem-estar de nossos colaboradores, o comprovante de vacinação COVID 19 é um item imprescindível para todos os empregados, estando presente na lista de documentos de admissão. “
#LI-LATAM
New Job Alerts
CPM Holdings, Inc.
Internal Sales Analyst- Industrial Solutions South America
São Paulo
FULL TIME
November 9, 2024
View Job DescriptionNovartis
Consultor Técnico Especialidades Sr. Pluvicto
Santo Amaro
FULL TIME
November 9, 2024
View Job DescriptionLooking for similar job?
Ultragenyx Pharmaceutical
Contract Regulatory Affairs Associate II (Analista Pleno), Brazil
São Paulo
FULL TIME
August 27, 2024
View Job DescriptionBNP Paribas
Senior Project / Program Manager (VP) – Regulatory
São Paulo
FULL TIME
September 11, 2024
View Job DescriptionNovo Nordisk
Regulatory Affairs Analyst (Black Community Inclusion)
São Paulo
October 4, 2024
View Job DescriptionSee What’s New: Sanofi US Job Opportunities
Sanofi US
Estágio em Country Quality CHC / Parque da Cidade/SP
São Paulo
October 29, 2024
View Job DescriptionSanofi US
Regulatory Affairs Team Manager - Vaga Exclusiva Para Pessoas com Deficiencia (PcD)
São Paulo
October 4, 2024
View Job DescriptionNew Job Alerts
CPM Holdings, Inc.
Internal Sales Analyst- Industrial Solutions South America
São Paulo
FULL TIME
November 9, 2024
View Job DescriptionNovartis
Consultor Técnico Especialidades Sr. Pluvicto
Santo Amaro
FULL TIME
November 9, 2024
View Job Description