Analista de Assuntos Regulatórios Sr at Cellera Farma responsible for regulatory documentation and compliance. Collaborating with internal teams to ensure product registration and market strategies.
Responsibilities
Responsible for preparing regulatory dossiers to obtain approvals for new products and to maintain portfolio products
Preparation of product registration and post-registration dossiers for submission to ANVISA
Experience with CTD-format dossiers
Review and approval of marketing/promotional materials
Review and approval of package inserts and labeling
Provide support to internal departments (marketing, manufacturing, R&D, etc.)
Monitor and interpret regulatory changes to anticipate impacts on the company’s business
Strategic market perspective with a focus on Regulatory Intelligence
Requirements
Bachelor’s degree in Pharmacy
Postgraduate education preferred
Intermediate English
Proven experience in the role interacting with regulatory authorities: ANVISA, VISA and other regulatory bodies, serving as a technical reference in the area
Strong command of legislation and standards: up-to-date, in-depth knowledge of sanitary legislation (RDCs, local and international standards)
Experience with product registrations and post-registration activities
Intermediate Microsoft Office skills
Strong verbal and written communication skills
Proactivity
Team player
Good interpersonal skills
Results-oriented
Autonomy
Ability to anticipate risks and provide strategic support for decision-making
Client commitment
Ability to apply and share knowledge
Change agent mentality
Discipline
Patience
Organizational skills
Analytical and detail-oriented mindset
Benefits
Monthly meal allowance
Medical and dental plans
Profit-sharing (PLR)
Home office policy (4x1)
Medication reimbursement policy
Childcare assistance
Life insurance
Year-end/Christmas allowance
Partnerships offering course discounts
Shuttle service (Campinas - Indaiatuba)
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