Rsi Manager Regulatory Affairs

**Job Function**:
Regulatory Affairs Group
**Job Sub Function**:
Regulatory Affairs
**Job Category**:
Professional
**All Job Posting Locations**:
Mexico City, Mexico, São Paulo, Brazil

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Regional Strategic Implementation (RSI) is part of the Regional Regulatory Affairs organization within Global Regulatory Affairs and supports regulatory activities in Asia Pacific (AP), Latin America (LA) and the Emerging Markets of EMEA. The team efficiently and effectively executes regional strategies and leverages processes and resources across all regions. We are therapeutically aligned and support the full lifecycle of products in all therapeutic areas.

**We are searching for the best talent for We are searching for the best talent for RSI Manager Regulatory Affairs - São Paulo-SP or Ciudad de México-MX**

Regional Strategic Implementation (RSI) is part of the Regional Regulatory Affairs organization within Global Regulatory Affairs and supports regulatory activities in Asia Pacific (AP), Latin America (LA) and the Emerging Markets of EMEA. The team efficiently and effectively executes regional strategies and leverages processes and resources across all regions. We are therapeutically aligned and support the full lifecycle of products in all therapeutic areas.

**Scope of Responsibilities**:

- Advises team on required documents in preparation of submissions as assigned in collaboration with RSI Lead.
- Assists with timely registration dossier availability, ensures that all document components are in place on time, identifies and tracks critical path activities;
- Compiles Module 1 for iCTDs to be dispatched to countries.
- Manages and tracks the assembly of country-specific submission packages to the LOCs in accordance with agreed plans.
- Participates in Working groups to ensure timely regional and local input into product objectives, to align regions with CDT/Global strategy.
- Interacts with the regional teams and Local Operating Companies to support regional and local activities.
- Drafts and reviews document content (depending on level of regulatory knowledge/expertise);
- Provides input to documentation to ensure they are in line with product strategy and thoroughly and accurately answers the questions being posed;
- Identify and initiate on-going continuous process improvement opportunities with end users responsible for data entry and/or data consumption.
- Advises team on required documents in preparation of Clinical Trial Applications (CTA)
- Provides operational support for the assembly and distribution of submissions ( e.g., CTA for China, Health Authority Responses).
- Support projects related to improved system functionality or to develop new business capabilities.
- Responsible for the critical review of submission documents to ensure compliance with regulatory requirements.
- Provides regulatory support for and appropriate follow-up to inspections, audits, litigation support and product complaints (depending on level of regulatory knowledge/expertise).
- Serves as the Regulatory representative on specific multi-discipline teams.
- Keeps abreast of current and pending approvals in specific therapeutic areas and is knowledgeable of laws, guidance and requirements related to those areas.
- Contributes to process improvement initiatives within and across functions.

**Qualifications**:

- A B.A./B.S. in science/relevant health-related discipline with an overall experience.
- Basic understanding of the product and registration life cycle from global regulatory affairs, local operating company or affiliates, and submission process perspectives is required.
- Knowledge of external factors (standards, regulatory requirements) that impact Product & Lifecycle Registration is preferred.
- Previous experience liaising with local, regional, and central regulatory users to ensure that new and ongoing regulatory requirements are reflected in the system configuration, functionality and business processes is highly preferred
- Demonstrated ability in working in global project teams in a matrix environment across multiple projects is required.
- Demonstrated ability to handle multiple projects.
- Excellent English verbal and written communication skills.
- Must have experience developing and maintaining strong relationships. Must have strong collaboration skills in order to partner effectively across other business units.