
Regulatory Biotech Dossier Manager
Há 4 dias
At Bayer, we work hard to make this company a better place for our employees - and the world a better place for everyone. "Health for all, hunger for none." That's our vision at Bayer.
Bayer is a global company with core competencies in the areas of life sciences, health care and agriculture. As an innovation company, we set trends in research-intensive areas. Bayer's products and services are designed to benefit people and improve their life quality.
**GET TO KNOW OUR AREA**:
We are part of the Regulatory Science team.
We ensure that the solutions we commercialize are safe for people and cause no undue harm to the environment.
We strive for regulatory approval of today's products and the technologies of tomorrow, being the enabler to business growth.
Our area is responsible to support Crop Science Brazil business developing and implementing regulatory strategies for innovations, life cycle management and regulatory defenses, in accordance with current legislation and internal policies and procedures.
**MAIN PURPOSE**:
The Regulatory Biotech Dossier Manager will be responsible for biotech dossier submissions in Brazil and will play a key role to develop and implement the cluster regulatory strategies for S&T innovations.
He/She must provide scientific and regulatory guidance to the Company for Biotechnology and Gene Editing areas in Brazil. The incumbent has the responsibility to elaborate, develop and implement the cluster regulatory strategies for high quality dossier submissions to secure trait approvals that will bring innovations across all biotechnology portfolio and future pipeline in Brazil. Responsible for strong coordination among global, regional and local multi-functional stakeholders, ensuring strategic communications through multiple channels available in R&D areas. Accountable for leading initiatives to engage understanding of local regulations and ensure the awareness of potential uncertainties in the regulatory environment and explore winning strategies to improve efficiency and reduce approval timelines.
**YOUR MISSION WILL BE TO**:
- Design strategies for biotech dossier elaboration and submission in Brazil, leading the scientific and regulatory discussions with local, regional and global functions;
- Accountable to build and implement Brazil regulatory guidance, strategies and best practices for new Traits development, lifecycle management projects in conjunction with Regional and Global strategies, ensuring competitive and timely approvals to meet short and long term business objectives. Guide the development of a solution in case of critical issues or delays;
- Work with relevant Bayer Crop Science functions to ensure necessary regulatory studies to secure the registration of new biotech products in Brazil and defense of our existing products and projects or third-parties products in a timely fashion;
- Oversee and support team members to collaborate with Regulatory Science and Biotech functions to facilitate dossier creation, mitigate regulatory and compliance risks with conditions of approvals;
- Responsible for obtaining and defending Trait portfolio registration activities, promoting Bayer's portfolio integrated solutions;
- Support the Senior Manager to ensure an effective communication with Local, Regional and Global Regulatory Managers to access technical information for dossier preparation and alignment with global PMO to deliver timely submissions and obtain import authorizations in Brazil;
- Provide regulatory information with adequate interpretation and guidance to relevant function/teams;
- Represents Bayer CropScience with regulatory authorities, lndustry association and internal and external Biotech forums, building and foster strong Partnership and contributing to modernize and shape the Brazilian regulatory environment in conjunction with key stakeholders;
- Actively participate at the different meetings and other regional and global company cross-functional networks to connect business needs with an effective regulatory strategy for biotech dossier submission;
- Provide advice to businesses on regulatory trends, decisions, their possible impact and how to respond. Anticipating new regulatory legislation and guidelines that may impact on the Bayer portfolio (development /marketed products) and influencing this;
- Responsible for the Post Market monitoring **(PMM) **planning and its execution. Including the negotiations with the third party companies that conducts the yearly survey, in case it is needed;
- Contributing to scientific papers publication to support the constant need for modernization of the local regulations, leveraging the scientific data produced in house and with external collaboration.
**ARE YOU READY FOR THE POSITION?**
**Must-Have skills**
- Ph.D. or M.Sc. Degree in Biology, Agronomy or a related Agricultural science, with In-depth knowledge in Molecular Biology, Biotechno
-
Biotech Regulatory Strategy Coordinator
Há 5 dias
São Paulo, São Paulo, Brasil beBeeRegulatory Tempo inteiro R$150.000 - R$190.000Job TitleThe Regulatory Biotech Dossier Coordinator is a key member of the team responsible for overseeing biotech dossier submissions in Brazil. They play a pivotal role in developing and implementing cluster regulatory strategies for S&T innovations.This position requires scientific and regulatory expertise to guide the company on Biotechnology and Gene...
-
Manager, Regulatory Affairs
Há 7 horas
São Paulo, São Paulo, Brasil buscojobs Brasil Tempo inteiroQuality Assurance Regulatory Affairs ManagerJob Summary: Highridge Medical creates the world's most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing to Core Spine. Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents...
-
Senior Regulatory Specialist
Há 2 dias
São Paulo, São Paulo, Brasil beBeeRegulatoryAffairs Tempo inteiro R$100.000 - R$150.000Regulatory Affairs SpecialistThe Role:We are seeking a highly skilled Regulatory Affairs Specialist to lead our regulatory strategy in Brazil.The ideal candidate will be responsible for ensuring compliance with Brazilian regulatory requirements, preparing and submitting regulatory dossiers, and managing market access.Main Responsibilities:Ensure Compliance...
-
Regulatory Affairs Professional
Há 5 dias
São Paulo, São Paulo, Brasil beBeeRegulatoryAffairs Tempo inteiro R$90.000 - R$120.000At the forefront of neuroscience, our mission is to defeat devastating neurological diseases through innovative scientific research. As a key member of our Regulatory Affairs team, you will play a vital role in ensuring timely business support by driving the creation and submission of high-quality dossiers for new medicines. This includes elaborating on...
-
Quality Assurance Regulatory Affairs Manager
3 semanas atrás
São Paulo, São Paulo, Brasil Highridge Medical Tempo inteiroQuality Assurance Regulatory Affairs ManagerQuality Assurance Regulatory Affairs ManagerGet AI-powered advice on this job and more exclusive features. Direct message the job poster from Highridge Medical Highridge Medical creates the world's most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing to Core Spine....
-
Senior Regulatory Compliance Manager
1 semana atrás
São Paulo, São Paulo, Brasil beBeeRegulatory Tempo inteiro R$60.000 - R$90.000Regulatory Affairs Lead Specialist\This role involves coordinating and ensuring the proper submission and approval of various medical devices or other categories of products to government regulatory agencies, while organizing and balancing a multitude of projects simultaneously.\- Coordinates the work of RA Specialists to ensure submission is done properly...
-
Chief Regulatory Compliance Officer
Há 6 dias
São Paulo, São Paulo, Brasil beBeeCompliance Tempo inteiro MX$2.500.000 - MX$3.500.000Regulatory Affairs LeaderWe are seeking a seasoned Regulatory Affairs expert to spearhead the development and execution of global regulatory strategies for our business vertical.The ideal candidate will possess a strong background in medical technology regulation, including pre-market approval processes, clinical trial oversight, and interaction with...
-
Quality Assurance Regulatory Affairs Manager
4 semanas atrás
São Paulo, São Paulo, Brasil Highridge Medical Tempo inteiroJob Summary: Highridge Medical creates the world's most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing to Core Spine. Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents to demonstrate Confidence in your work and...
-
São Paulo, São Paulo, Brasil Highridge Medical Tempo inteiro US$100.000 - US$160.000 por anoJob Summary:Highridge Medical creates the world's most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing to Core Spine. Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents to demonstrate Confidence in your work and...
-
Regulatory Affairs Manager
1 dia atrás
São Paulo, São Paulo, Brasil Essity Tempo inteiro**Regulatory Affairs Manager LATAM**:**Trabalhar na Essity não é apenas uma carreira, é uma chance de tornar o mundo um lugar mais saudável, higiênico e seguro. Com inovações impactantes, juntamente com soluções sustentáveis, nos esforçamos para alcançar mais pessoas a cada ano com as soluções necessárias e essenciais para o bem-estar.****A...