8 Empregos para Epa - Brasil

Manager, Regulatory Affairs

J&J Family of Companies

Publicado há 4 dias atrás

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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Regulatory Affairs Group
**Job Sub** **Function:**
Regulatory Affairs
**Job Category:**
Professional
**All Job Posting Locations:**
São José dos Campos, São Paulo, Brazil, São Paulo, Brazil
**Job Description:**
The Manager, Regulatory Affairs leads a team of individual contributors and is accountable for conducting effective performance management. The manager is also responsible for regulatory strategies that support the execution of the Wound Closure and Healing portfolio strategy and regularizing the Brazilian manufactured products, ensuring compliance to local and international regulations and ensuring business continuity through the maintenance of compliant and accurate registrations / sanitary licenses. The individual will have end to end responsibility for maintaining existing products in key markets and launch of new/improved products in alignment with portfolio strategy. The Manger will be strategic by considering new and changing regulatory requirements to identify the most effective and efficient strategies for compliance. This position is also responsible for providing direction and leadership to RA team members in the development and execution of global regulatory strategies and processes to ensure timely registration of Wound Closure and Healing products globally.
**DUTIES & RESPONSIBILITIES***
Under limited supervision and general direction in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
- Coordinates the production and compilation of the required documentation to legally regulate the sanitary registration of the products manufactured in Brazil, in the countries of Latin America (LATAM), Asia, Europe, Africa and USA, and when applicable, carry out the registers directly in the countries of interest.
- Ensure that documentation of products manufactured by Brazil is available when and where customers need it, providing guidance to technical areas, preparing documents in compliance with regulatory requirements, to support both local and international registration, and marketing of the products. products in the public market (biddings) and in the private sector.
- Participate in key projects of the SJDC site, delivering strategies and regulatory results within the agreed time frame in the project schedule.
- Identify and anticipate changes in the national and international health regulatory environment of interest and impact on the business or products of the SJDC site to support the implementation of new or changed health regulations / standards to ensure that the site's products, processes, practices and procedures of SJDC are in compliance therewith.
- Keep updated under the regulatory sanitary aspect, procedures and approvals in the systems of use by the site of SJDC, such as EtQ, Barcode, ADAPTIV, and MDRiM which includes the Preliminary and Final Regulatory assessment, if applicable.
- Interact, establish and maintain communication with health authorities and notified bodies, such as ANVISA, BSI, SABS, TGA and others directly related to the activities of the SJDC site.
- Participate as representative of the Company in national or international forums for discussion and creation of sanitary standards and regulations, of business interest, to contribute positively to the Brazilian regulatory environment.
- Maintain up-to-date licenses / certificates / health authorizations required for the SJC site operations.
- Support inspections, audits, field actions, site-related techno-surveillance, and products manufactured by SJDC.
- Establish strong connections and collaboration with business partners at SJDC and ETHICON USA, such as quality, legal, packaging, manufacturing, market, regulatory affairs.
- Ensure subordinates follow all company guidelines related to Environmental, Health, and Safety practices, and that all resources needed are available and in good condition, if applicable.
- Empower team to act with speed, agility, and accountability.
**EXPERIENCE AND EDUCATION***
- Degree in Pharmacy or related areas.
- A minimum of 8 years of working in a Regulatory Affairs preparing submissions for complex devices or other product categories.
· Fluent English.
- Spanish desirable.
· Active affiliation with CRF-SP, able to assume a technical responsible role
- Multi country experience desirable.
- Experience 1 - 2 years direct management.
- Knowledge of regulatory environment such as Brazilian Directives, Medical Devices Directive (MDD), FDA regulations and others
- Analytical problem-solving skills
- Ability to partner within the team and across teams
- Strong communication and presentation skills
- Critical thinking and ability to partner with key stakeholders
· Strong interpersonal and analytical skills to understand technical data/information
**LOCATION AND TRAVEL REQUIREMENTS**
- Position based in Sao Jose dos Campos or Sao Paulo
- Occasional travel for domestic and/or international territories.
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Regulatory Affairs Specialist

ICON Clinical Research

Publicado há 5 dias atrás

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Regulatory Affairs Specialist - São Paulo
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Regulatory Affairs Specialist to join our diverse and dynamic team. As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
**What you will be doing**
+ Undertaking variable duties based on project requirements, primarily within Pharmaceutical, BiotechNlogy, or Biologics Regulatory Affairs, with potential involvement in related areas.
+ Contributing to regulatory submissions team activities, including preparation, compilation, and submission of regulatory documents such as CT/IND, MAA/NA, variations/lifecycle submissions, DSUR, PSUR, renewals, and agency briefing documentation.
+ Managing and implementing label review, translation requirements, fee calculations, and other aspects for regulatory submissions.
+ Providing input to the Regulatory Intelligence function and participating in readability testing.
+ Reviewing IMPD/IB Core Docs and labeling for clinical trials.
+ Collaborating with Regulatory Submissions team or cross-functional teams based on project size and nature.
+ Facilitating business development activities as needed.
**Your profile**
+ Bachelor's degree in a scientific or healthcare-related field; advanced degree preferred.
+ Minimum of 2-3 years of experience in regulatory affairs within the pharmaceutical or biotechNlogy industry.
+ Proficiency in regulatory submission processes and requirements, including CT/IND, MAA/NA, variations, DSUR, PSUR, and renewals.
+ Familiarity with label review, translation requirements, and regulatory intelligence activities.
+ Strong attention to detail and excellent communication skills.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
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Expert, Regulatory Affairs, GO, P&B

dsm-firmenich

Publicado há 11 dias atrás

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**Job Title: Expert Regulatory Affairs,GO,P&B (São Paulo, Cotia)**
**City: São Paulo, Cotia.**
As Expert Regulatory Affairs,GO,P&B you will be responsible for building and strengthening relationships of trust and intimacy with both internal and external customers in local and regional (LAM) markets, in alignment with DSM-Firmenich P&B business needs.
Internal customers will include local and regional (LAM) sales teams, as well as creative and innovative functions. External customers will include local, regional (LAM), and global clients.
Additionally, you will serve as a liaison between the Regulatory Affairs teams and both internal and external clients; you will ensure alignment with the Brazilian fragrance trade association advocacy groups on all relevant aspects of DSM-Firmenich policy, while also representing and promoting the concerns and needs of DSM-Firmenich's business.
At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated.
**Your key responsibilities**
+ Develop and maintain internal and external customer relationships in alignment with P&B business plans, while providing local and regional (LAM) support on all aspects of compliance related to DSM-Firmenich's Perfumery and Ingredients portfolio.
+ Develop and maintain expertise in local and regional (LAM) compliance requirements, advocating clearly and effectively both externally and internally.
+ Support the regional Senior manager in implementing changes when client, government or industry standards take place. Guide the group data compliance team in database implementation and ensure the proper deployment of the requirements to ensure compliance (including development of impact assessments, communications, questionnaires/documents adaptation)
+ Support the regional senior manager in regulatory strategic meetings with internal/external customer, trade associations and other regulatory/business stakeholders
+ Communicate agreed-upon positions with both internal and external customers.
**You Bring**
+ Able to understand what is needed to guide and support business strategy, contribute to longer term plans and deliver
+ Can integrate creative and business thinking into delivering solutions
+ Masters verbal, non-verbal and written communication skills (can adapt between presenting technical details and using everyday language for complex issues).
+ Acts as a change champion, not only with successfully implementing change through trainings and communications but continuously looking for ways to improve Regulatory affairs level of support to the business.
+ Uses emotional intelligence to act as a supportive expert with internal/external customers
**We Bring**
+ A space to grow by encouraging and supporting curiosity and an open mindset.
+ A culture that prioritizes safety and well-being, both physically and mentally.
+ The opportunity to work for a company where sustainability is much more than a claim and is core to our strategy and purpose.
+ A firm belief that working together with our customers is the key to achieving great things.
+ An eagerness to be one team and learn from each other to bring progress to life and create a better future.
+ A flexible work environment that empowers people to take accountability for their work and own the outcome.
+ Background in Regulatory Affairs within the Fragrance and Flavour industry.
+ Good knowledge of fragrance, cosmetics and chemicals regulations.
+ Good professional level of English. Spanish communication skills would be appreciated.
**How to apply**
Interested in this job? Apply online by submitting your resume through our career portal. Generally, the procedure will be in line with the application process described on the dsm-firmenich careers website. Due to privacy regulations, we can only actively interact with applications through the career portal. For further information, please contact (TAP name), (e-mail).
**Equal opportunities commitment**
dsm-firmenich is fully dedicated to inclusion because when people feel engaged and empowered, their creativity and innovation drives unprecedented progress. We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate: (here,) there's a place for everyone with us.
dsm-firmenich is an Equal Opportunity and Affirmative Action Employer. Our people are as diverse as our customers. For us that includes a commitment to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law.
We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know.
**About dsm-firmenich**
As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world's growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet. dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.
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Regulatory Affairs Director LATAM - Medical Devices (m/f/d)

São Paulo, São Paulo Abbott

Publicado há 27 dias atrás

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At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world in nutrition, diagnostics, medical devices and branded generic pharmaceuticals that create more possibilities for more people at all stages of life. Today, 114,000 of us are working to help people live not just longer, but better, in the more than 160 countries we serve.
Abbott is currently looking to recruit a
**Regulatory Affairs Director LATAM - Medical Devices (m/f/d)**
_Based in São Paulo, Brazil_
This position is responsible for the development and direction of the Regulatory Affairs team in Latin America to obtain necessary approvals and licenses to increase and maintain the portfolio of following Medical Device divisions: CRM / EP / HF / SH / NM / VAS.
**MAIN RESPONSIBILITIES:**
- Define regulatory strategies and align resources to execute essential regulatory tasks in a timely manner, ensuring no business disruption in the region.
- Provide the best regulatory solutions for each business model in the region, covering both direct subsidiaries and multi-distributor networks.
- Hire, train, and support the Regulatory Affairs team and determine the optimal organizational structure to meet group objectives.
- Build strong relationships with Health Authorities and other external stakeholders. Act proactively with these Health Authorities in the region to shape and implement emerging regulations without business disruption. Monitor these new regulations, analyze their impact, determine implementation strategies, and ensure proper documentation in company systems.
- Maintain close collaboration with Marketing, Operations, and Sales teams to ensure compliant product launches according to local regulations.
- Align team responsibilities and activities with the demands of business units and senior Regulatory Affairs leadership.
- Ensure that Regulatory Projects in the region are properly managed and resourced to promote continuous improvement of regulatory processes.
- Identify opportunities, anticipate risks, and enable effective contingency plans when necessary to achieve goals and accelerate opportunities.
- Continuously monitor the competitive landscape and provide valuable regulatory insights for business planning.
- Build personal credibility and strong working relationships capable of engaging and/or leading high-performance cross-functional teams.
- Manage regional budget and resources.
- Ensure compliance with activity metrics under your responsibility, as well as internal/external customer satisfaction, and implement corrective or preventive actions when necessary.
- Conduct actions and decisions under your responsibility in accordance with the company's Code of Business Conduct.
- Support EHS (Environment, Health, and Safety) policies and practices by participating in and promoting area initiatives.
**EDUCATION:**
- Bachelor´s Degree in Biomedical Science, Pharmacy, Biomedical Engineering, or a related field.
- Fluent English & Portuguese, intermediate/advanced level in Spanish
**EXPERIENCE:**
- Minimum of 10 years of experience in Regulatory Affairs of medical devices.
- At least 5 years of experience in a supervisory/managerial level with proven success in a highly matrixed environment.
- Track record in working with trade associations in the region
**COMPETENCIES:**
- Ability to build partnerships and collaborate across organizations, regions, and with external partners to achieve results.
- Strong influencing skills with stakeholders across different areas/functions.
- In-depth knowledge of Medical Device regulations in Latin America.
- Excellent verbal and written communication skills.
- Strong negotiation and persuasion abilities.
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Especialista em Meio Ambiente , Environmental Assurance & Protection (EAP)

Betim, Minas Gerais Amazon

Publicado há 17 dias atrás

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Description
Our team is seeking an Environmental Specialist responsible for managing environmental compliance at our operations in MG.
Key job responsibilities
- Execute site environmental procedures and ensure compliance with all applicable federal, state, regional, and local regulations;
- Manage and execute site responsibilities to comply with air emissions, surface water, wastewater, waste, and other environmental laws, regulations, and permits;
- Prepare and manage site-specific environmental reports to regulators and within Amazon;
- Manage and execute waste activities, including classification, reporting, and permitting requirements;
- Conduct waste and surface water inspections at the site;
- Monitor and provide guidance on site performance against applicable environmental regulations, programs, and Amazon global standards;
- Analyze environmental metrics and review weekly and monthly trends to identify areas for improvement;
- Perform site-specific tasks related to the implementation of Environmental Program Assessments;
- Support the measurement and analysis of site performance against environmental procedure requirements and develop plans to address any identified deficiencies;
- Execute relevant environmental procedures as required by business or regulatory needs;
- Support the evaluation and development of process improvements to mitigate identified risks;
- Assist in conducting root cause analyses for environmental incidents and recommend appropriate corrective actions for network-wide implementation;
- Identify and implement corrective actions to eliminate any observed or potential non-compliance situations.
A day in the life
You will assist in the implementation and enforcement of standards and policies to support environmental and regulatory compliance, and will provide guidance to operations, maintenance, and construction teams.
About the team
The Environmental Assurance and Protection team protects Amazon businesses and supports the needs of our customers by proactively mitigating environmental regulatory risks and protecting the environment.
Basic Qualifications
- Bachelor's degree
- Experience serving as an environmental technical resource, environmental specialist;
- Experience using knowledge of federal, state and municipal regulations;
- Experience engaging with Regulatory Agencies.
Preferred Qualifications
- Knowledge of Microsoft Office products and applications and the use of pivot tables and the development of charts and graphics
- Experience in warehouse operations and logistics or equivalent
- Bachelor's Degree in civil, chemical or environmental engineering or related field of environmental studies;
- Broad knowledge of BR and local environmental regulations;
- Experience profiling and managing hazardous and non hazardous waste;
- Advanced English will be a differential.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.
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Técnico ambiental, Environmental Assurance and Protection (EAP)

Cajamar, São Paulo Amazon

Publicado há 6 dias atrás

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Description
A Amazon está à procura de uma pessoa para atuar como representante ambiental nas operações do site. A pessoa prestará apoio na execução e implementação dos programas relacionados à gestão de resíduos da equipe de Environmental, Assurance & Protection Global (EAP) no site atribuído.
Key job responsibilities
- Caracterização/determinação de resíduos incluindo segregação adequada, armazenamento, rotulagem e preparação para destinação, de acordo com exigências federais, estaduais e municipais;
- Manutenção física e organização das áreas de armazenamento/gestão de resíduos e de todas as áreas de acumulação satélite, de acordo com os requisitos regulamentares e políticas aplicáveis da Amazon;
- Realizar auditorias ambientais completas e precisas para melhoria contínua, incluindo, entre outros, pontos diários de coleta de resíduos, kits de resposta a derramamentos, área de Product Awaiting Determination, suprimentos para gerenciamento de resíduos, etc.;
- Priorizar e gerenciar diversas tarefas simultaneamente;
- Responder à limpeza de pequenos derramamentos ambientais nas operações de triagem, docas e pátios;
- Participar de todas as investigações relativas à incidentes ambientais no site; Trabalhar em estreita colaboração com a equipe de EAP Field para conduzir investigações completas e precisas de incidentes ambientais e desenvolver ações corretivas apropriadas;
- Coordenar e apoiar todas as destinações de resíduos, bem como, ser o ponto de contato local para os fornecedores de resíduos;
- Gerenciar equipamentos, recipientes, rótulos e outros suprimentos do fornecedor de resíduos ou de outros fornecedores para manter níveis de estoque adequados; - Garantir a geração e manutenção dos registros necessários quanto à geração de resíduos de acordo com os requisitos regulamentares e pela política Amazon, incluindo inspeções de rotina que atendam aos prazos estabelecidos;
- Interação com equipes de WHS, ICQA, ISS, RME e outras equipes do site responsáveis pela gestão adequada de produtos químicos perigosos e geração de resíduos perigosos e não perigosos; - Apoiar a equipe EAP Field na preparação do inventário mensal de resíduos e na identificação da frequência de envio necessária para cumprir os requisitos de acumulação;
- Pesquisar tendências, perdas de estoque e esforços de redução de custos, quando aplicável;
- Atuar como recurso para fornecer treinamento e responder perguntas relacionadas ao gerenciamento de resíduos das operações, conforme a necessidade do site.
Basic Qualifications
- Ensino médio completo.
- Experiência com produtos e aplicativos do Microsoft Office (tabelas dinâmicas e desenvolvimento de tabelas e gráficos).
- Conhecimentos básicos em gestão de resíduos.
Preferred Qualifications
- Experiência na gestão de aspectos ambientais
- Técnico ambiental completo
- Conhecimento das regulamentações ambientais locais
- Experiência em gerenciar resíduos perigosos e não perigosos
- Experiência em operações de armazém e logística será um diferencial
- Inglês básico será um diferencial
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.
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Técnico ambiental, Environmental Assurance and Protection (EAP)

Cajamar, São Paulo Amazon

Publicado há 11 dias atrás

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Description
A Amazon está à procura de uma pessoa para atuar como representante ambiental nas operações do site. A pessoa prestará apoio na execução e implementação dos programas relacionados à gestão de resíduos da equipe de Environmental, Assurance & Protection Global (EAP) no site atribuído.
Key job responsibilities
- Caracterização/determinação de resíduos incluindo segregação adequada, armazenamento, rotulagem e preparação para destinação, de acordo com exigências federais, estaduais e municipais;
- Manutenção física e organização das áreas de armazenamento/gestão de resíduos e de todas as áreas de acumulação satélite, de acordo com os requisitos regulamentares e políticas aplicáveis da Amazon;
- Realizar auditorias ambientais completas e precisas para melhoria contínua, incluindo, entre outros, pontos diários de coleta de resíduos, kits de resposta a derramamentos, área de Product Awaiting Determination, suprimentos para gerenciamento de resíduos, etc.;
- Priorizar e gerenciar diversas tarefas simultaneamente;
- Responder à limpeza de pequenos derramamentos ambientais nas operações de triagem, docas e pátios;
- Participar de todas as investigações relativas à incidentes ambientais no site; Trabalhar em estreita colaboração com a equipe de EAP Field para conduzir investigações completas e precisas de incidentes ambientais e desenvolver ações corretivas apropriadas;
- Coordenar e apoiar todas as destinações de resíduos, bem como, ser o ponto de contato local para os fornecedores de resíduos;
- Gerenciar equipamentos, recipientes, rótulos e outros suprimentos do fornecedor de resíduos ou de outros fornecedores para manter níveis de estoque adequados; - Garantir a geração e manutenção dos registros necessários quanto à geração de resíduos de acordo com os requisitos regulamentares e pela política Amazon, incluindo inspeções de rotina que atendam aos prazos estabelecidos;
- Interação com equipes de WHS, ICQA, ISS, RME e outras equipes do site responsáveis pela gestão adequada de produtos químicos perigosos e geração de resíduos perigosos e não perigosos; - Apoiar a equipe EAP Field na preparação do inventário mensal de resíduos e na identificação da frequência de envio necessária para cumprir os requisitos de acumulação;
- Pesquisar tendências, perdas de estoque e esforços de redução de custos, quando aplicável;
- Atuar como recurso para fornecer treinamento e responder perguntas relacionadas ao gerenciamento de resíduos das operações, conforme a necessidade do site.
Basic Qualifications
- Ensino médio completo.
- Experiência com produtos e aplicativos do Microsoft Office (tabelas dinâmicas e desenvolvimento de tabelas e gráficos).
- Conhecimentos básicos em gestão de resíduos.
Preferred Qualifications
- Experiência na gestão de aspectos ambientais
- Técnico ambiental completo
- Conhecimento das regulamentações ambientais locais
- Experiência em gerenciar resíduos perigosos e não perigosos
- Experiência em operações de armazém e logística será um diferencial
- Inglês básico será um diferencial
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.
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Engenheiro(a) de Meio Ambiente, Environmental Assurance and Protection (EAP)

Brasília, Distrito Federal Amazon

Publicado há 4 dias atrás

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Description
Brazil´s Environmental Assurance and Protection (EAP) team is seeking a Multi-Site Environmental Engineer to support our Amazon Operations. This role supports multiple sites. The person will develop standards and policies to support regulatory compliance as well as partner with operations leadership teams for execution of these standards and policies, to ensure compliance with all applicable county/locations specific Federal, State and local laws and regulations. The person travels greater than 50% of the time.
Key job responsibilities
- Manage and execute multi-site responsibilities to comply with stormwater, waste, wastewater and other environmental related laws, regulations and permits. This includes required Federal, State and local reporting.
- Manage and execute business conformance with Amazon EAP Management Systems policies. Develop Amazon Geo-Specific Operational Environmental Procedures by integrating with engineering, construction and operations.
- Lead regulatory agency interactions, permit evaluation and processing, and new process and technology introduction.
- Primary point of contact for environmental regulatory agencies and represents Amazon at appropriate levels with governmental agencies and throughout the company.
- Ensure work performed by contractors, consultants, and employees is completed in accordance with regulatory requirements and Amazon standards.
- Monitor environmental metrics to review trends to determine where improvements are needed.
- Conduct thorough and accurate environmental inspections and audits for continuous improvement.
- Prioritize and manage multiple, technically complex assignments, concurrently.
- Build and manage collaborative relationships with various stakeholders to ensure risks are identified early and managed appropriately.
- Compile and submit time critical reports to various governmental agencies.
- Complete thorough and accurate environmental incident investigations and associated regulatory reports, and develop appropriate corrective actions.
- Ensure site leadership and associates are trained and knowledgeable of their responsibilities under each policy.
A day in the life
The person will complete environmental performance analysis, establish and monitor metrics, and guide the operations leadership teams in implementation of Amazon environmental standards. The person will work with internal and external partners that include government entities, contractors, consultants, design, construction, operations and other key stakeholders.
About the team
The EAP organization protects Amazon businesses and supports the needs of our customers by proactively mitigating environmental regulatory risks and protecting the environment.
Basic Qualifications
- Bachelor's degree
- Fluent in English B2;
- Experience serving as an environmental technical resource, program specialist, or program manager .
Preferred Qualifications
- Bachelor's degree in environmental, chemical or industrial engineering, environmental science or related field of study.
- Experience serving as an environmental technical resource, regional manager, program specialist, and/or program manager
- Experience using written and verbal communication skills, including comfort interfacing with site and regional leaders
- Knowledge of Mexican state and federal environmental regulations
- Experience engaging with Regulatory Agency in permit application and regulatory inspection responses
- Experience engaging with Regulatory Agency in permit application and regulatory inspection responses
- Broad knowledge of local, state, and federal environmental regulations
- Experience implementing environmental systems
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.
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  5. paletteArtes e Entretenimento
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  10. account_balanceBanca e Finanças
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  14. point_of_saleComercial e Vendas
  15. shopping_cartCompras
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  17. supervisor_accountConsultoria de Gestão
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  20. brushCriativo e Digital
  21. currency_bitcoinCriptomoedas e Blockchain
  22. child_friendlyCuidados Infantis
  23. shopping_cartE-commerce e Redes Sociais
  24. schoolEducação e Ensino
  25. boltEnergia
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  64. petsVeterinária
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