8 Ofertas de Scientist Ii Regulatory Affairs Global Imports & en Tlalnepantla

**Job Description**
**Are You Ready to Make It Happen at Mondelēz International?**
**Join our Mission to Lead the Future of Snacking. Make It With Pride.**
You execute the regulatory affairs strategy for your respective categories and geographical area using your technical and regulatory expertise. You ensure the regulatory and policy compliance of our portfolio and ensure policies, regulatory programs and requirements are met.
**How you will contribute**
You will implement the regulatory affairs strategy and work with cross-functional teams to anticipate regulatory business risks and opportunities. In addition, you will provide regulatory affairs expertise for technical regulatory developments and help with responses to challenges and crisis management. In this role, you will ensure that ingredients, product composition, claims and labelling is in compliance with regulations and company policies, provide guidance to stakeholders on regulatory affairs, propose and implement business solutions in response to regulatory changes, and maintain and develop a strong knowledge of regulatory, scientific and nutrition risks and opportunities in your corresponding market.
**What you will bring**
A desire to drive your future and purpose, accelerate your career and the following experience and knowledge:
+ Regulatory affairs (industry, governmental, association background).
+ Understanding of the regulatory framework in your geographical area
+ Building collaborative relationships
+ Conducting technical assessments and supporting issues management
+ Thinking creatively
+ Communicating effectively
+ Project management
+ SARA core knowledge topics (e.g. flavors, additives, GMO, organic, dietary or religious suitability, etc.)
**What you will bring**
A desire to drive your future and purpose, accelerate your career and the following experience and knowledge:
Regulatory affairs (industry, governmental, and association background).
Understanding of the regulatory framework in your geographical area
Building collaborative relationships
Conducting technical assessments and supporting issues management
Thinking creatively
Communicating effectively
Project management
SARA core knowledge topics (e.g. flavors, additives, GMO, organic, dietary or religious suitability, etc.)
**More about this role**
The position is with the North American Regulatory Ingredients and Global Import Export team.
The scope of work includes reviewing and coordinating the revision of ingredient compliance against US FDA and Health Canada requirements and ensuring regulatory information excellence in the ingredient specifications.
Ability to interpret complex ingredient regulations and laws for food and recommend compliance strategies that balance risk with business impact and cost.
Experience with PLM is a requirement. Experience with MS Teams and other MS Apps is an asset.
The role will also be responsible for GIE RA brand/category continuity, leading the strategy and decision-making, adapting to the business needs.
Strong organization and leadership, acting like an owner, proactively collaborating with business partners and regulatory colleagues to develop strategies and recommended action plans to advance complex business initiatives.
Work autonomously and through others to facilitate deployment/ delivery of all regulatory project elements (compliance, claims, labeling) as required.
Interface and collaborate across different functions of the organization to ensure project outcomes are achieved with high-quality results and gain their alignment and support.
This candidate will be expected to be involved in and make contributions to the North American SARA community/pillars/programs/tools.
**Education / Certifications:**
Bachelor's degree in nutrition, Food Science, or related scientific discipline
**Job-specific requirements**
Desired experience with US FDA and Health Canada food regulations, specifications, and labeling databases.
**Work schedule:**
Regular business hours
**Work schedule: Full time**
No Relocation support available
**Business Unit Summary**
**Mondelēz International is the world's largest chocolate, biscuit and candy maker, and the second largest gum maker. Our North American and U.S. headquarters are in East Hanover, New Jersey, about 25 miles outside of New York City. We have Canadian offices in Toronto and Montreal. We have a strong North American manufacturing presence where we make our well-loved snacks like** **_Oreo_** **cookies,** **_belVita_** **breakfast biscuits,** **_Trident_** **gum and** **_Cadbury_** **chocolates. Our East Hanover location also houses our global research and development center for our consumer-favorite cookie and cracker brands.**
USA:
Mondelēz Global LLC is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants who require accommodation to participate in the job application process may contact for assistance.
Canada:
If you are applying to a position in Canada, accommodations for applicants with disabilities or other grounds protected by human rights legislation are available upon request for candidates taking part in all aspects of the employment selection process. For all internal and external applicants who require accommodation in the recruitment and selection process please contact for assistance/support.
**Job Type**
Regular
Scientific Affairs & Regulatory Affairs
Product Quality, Safety and Compliance
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about.
We have a rich portfolio of strong brands - both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum
Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast.
Join us and Make It An Opportunity!
Mondelez Global LLC is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants who require accommodation to participate in the job application process may contact for assistance.

**Global Regulatory Affairs LCM&E**

**Major Tasks**

1) Responsibility for the regulatory strategy with regard to Chemistry Manufacturing and Controls (CMC) for assigned products in close cooperation with the relevant global, regional, and country RA functions, BHC ProductSupply, Medical, Drug Safety and Marketing, to ensure early identification of major regulatory hurdles and issues with regard to CMC related topics, regulatory guidelines and legal requirements, and coordination of respective corrective actions. Provides active input into GRTs for assigned projects to ensure timely submission and first cycle approval.

2) Responsibility for timely availability and final content of CMC IND/IMPD, NDA/MAA-, sNDA-, or BLA-submissions for assigned productsto Health Authorities, including responses to health authority questions.

3) Responsibility for the CMC change management for assigned development and marketed products, which includes providing regulatory assessments, tracking of CMC changesand processing of requests for related documentation(evaluation, consolidation, prioritization and review), responsibility for coordination of responses to health authority questions, and for implementation of CMC changes after HA approvals with product supply, to ensure regulatory CMC compliance.

4) Ensures adequate surveillance of the CMC-related regulatory environment for assigned products and anticipates and influences changes in this environment globally.

5) Manages scientific support of assigned marketed products with respect to regulatory aspects and Labeling in close cooperation with the respective TA heads.

6) Coordinates and ensures the timely generation of regulatory documents adhering to global, regional and local requirements.

7) Responsibility for the support of assigned marketed products to ensure the successful maintenance of and life-cycle (variations, renewals or deficiency letter), ensuring regulatory guidelines are met.

8) Manages the preparation of registration dossiers related to assigned products and proactively identifies and tracks regulatory activities and /or issues and risks and brings these to the attention of RA CC infrastructure management as necessary

9) Coordinates the publishing and dispatching activities of the variations to the respective local regulatory affairs as well as submitting through EU gateway.

**Skills**
- Education - Ph.D., M.D., or PharmD degree in life sciences with a 2+ years of regulatory experience ; or MS with a 4+ years of Regulatory experience, or a Bachelor’s degree 6+ years’ of regulatory experience. - 2+ years of regulatory experience in Pharmaceutical Industry Competencies
- Excellent oral and written communication skills.
- Well developed management and leadership skills, as incumbent has to lead multidisciplinary teams. Demonstrated cross-functional communication, interpersonal, influence, and negotiation skills
- Ability to focuson multiple issues at one time, and to organize and direct diverse activities in a changing environment often under time pressure. Job holder must be able to work focused and target oriented in a complex scientific / technical environment. -Ability to harmonize and reconcile competing objectives to achieve the overall objectives. - Thorough knowledge of company policies and procedures in maintenance

**Período de aplicación**:
24 Febrero al 10 Marzo
**Código de referencia**:


**División**:
Consumer Health
**Ubicación**:
Mexico : Ciudad de México : Ciudad de México

**Área funcional**:
Registro Farmacéutico
**Grado de posición**:
VS 1.1

**Tipo de empleo**:
Permanente
**Tiempo de trabajo**:
Full Time

Job Description:
Collaborate with innovative 3Mers around the world

As Regulatory Affairs Specialist you will play a key role for coordinating regulatory strategy for Mexico in the division of Consumer Health Group. In this role you will be able to provide support and expertise as part of the Regulatory organization using knowledge of Mexican regulatory requirements and paths to support achievement of business objectives.

The impact you will make in this role
- Prepare Technical Documentation for Consumer Health products
- Assure that all device listings, establishment licenses, and registrations for Consumer Health products are accurate and up to date
- Advise on new regulatory strategies and regulatory changes.
- Review product labeling and claims for compliance to applicable regulations
- Represent Regulatory Affairs on multidisciplinary project teams including New Product Introductions and Change Management Projects
- Business and Distribution regulatory assistance as required
- Interface with local agency COFEPRIS.
- Participate and provide support to Mexican Regulatory
- Ensure compliance with applicable regulatory requirements including those pertaining to product safety and post-market surveillance / vigilance
- Support other LATAM area consultancy agreements and resourcing plans as required
- Ensures compliance with marketer Licenses.

Your Skills and Expertise
- In depth knowledge of health legislation in Mexico for Medical Devices such as LGS, RIS, FEUM Medical Devices Supplement, Oficial Mexican Standar´s NOM-241-SSA1, NOM-137-SSA1, NOM-240-SSA1, and other related.
- Knowledge of LGS regulations regarding advertising
- At least (5) years of experience in direct submissions before COFEPRIS such a modification to the registration conditions, obtaining new registrations, electronic renewals, and advertising permits for web pages and medical devices.
- Classification and regulatory requirements for low risk devices, Class I, Class II, sterile products.
- Ability to communicate effectively with the Health Authority.
- Experience as Sanitary Responsible preferred.
- Bachelor’s degree or higher (completed and verified prior to start)
- Combined experience in Regulatory
- Advanced English speaking skillsets
- Available to work In México City.

Supporting Your Well-being

3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope.

Imagine your future in 3M

3M es un empleador que ofrece las mismas oportunidades. 3M no discriminará a ningún solicitante de empleo por razones de raza, color, edad, religión, sexo, orientación sexual, identidad o expresión de género, origen nacional, discapacidad o estado de veterano.

3M Global Terms of Use and Privacy Statement

At Beiersdorf, we want to help people feel good about their skin - and our commitment goes far beyond caring for skin. For 140 years, we have developed innovative skin and body care products for well-known brands such as NIVEA, Eucerin, La Prairie, Hansaplast, and Labello. We act according to our purpose, WE CARE BEYOND SKIN, and take responsibility for our consumers, our employees, the environment and society.

Behind every brand, every product and every accomplishment are our more than 20,000 employees. It is for them that we live a culture of inclusion, respect and trust that is strongly aligned with our values - CARE, COURAGE, SIMPLICITY and TRUST. We embrace diversity by valuing the uniqueness of each individual and being committed to equal opportunities for all.

**Your Tasks**:

- Asegurar la correcta ejecución de las estrategias regionales de Health Care en cada uno de los países de Latinoamérica a través del desarrollo y establecimiento de la estrategia regulatoria correcta y ágil para registro de dispositivos médicos y medicamentos.
- Liderar y Coordinar con BSN Medical Cali la disponibilidad de todos los documentos requeridos para asegurar un proceso de registro, actualización o renovación exitoso del portafolio Curitas en países de Latinoamérica y algunos del Medio Oriente, así como de coordinar la correcta implementación de los artes aprobados para venta.
- Responsable por asegurar y proporcionar información técnica y documentos legales necesarios para llevar a cabo los registros de los productos como dispositivos médicos o medicamentos en los diferentes países de Latinoamérica, brindando soporte y guía a los equipos regulatorios locales.
- Responsable de coordinar la revisión regulatoria de artes para garantizar el cumplimiento con la legislación aplicable en cada uno de los países de Latinoamérica.
- Responsable directo por la revisión y aprobación de artes, claims, material publicitario y promocional para asegurar que cumple con los lineamientos aplicables vigentes por COFEPRIS en México.
- Responsable por obtener los registros sanitarios del portafolio de Health ante COFEPRIS en México, así como de mantener el plan anual de actualización, mantenimiento y renovación oportuna de los registros.
- Responsable por obtener los permisos de importación, permisos de publicidad y avisos de publicidad ante COFEPRIS en México.
- Informar de manera oportuna sobre los cambios en la legislación y normativa mexicana que puedan impactar de forma directa la importación, almacenamiento, distribución, comercialización y/o venta en México.
- Mantener contacto directo con los equipos regulatorios locales para anticipar riesgos por cambio de sus regulaciones que puedan impactar la importación, almacenamiento, distribución, comercialización y/o venta en México y los países de Latinoamérica.

**Your Profile**:

- Carreras: Ciencias de la salud, farmacéutico, ingeniero químico, ingeniero industrial
- Mínimo 3 años de experiência en posición similar
- Inglés intermedio
- Manejo de trámites Regulatorios ante COFEPRIS, registros sanitarios de Dispositivos Médicos y/o Medicamentos.
- Conocimiento de la normatividad aplicable a dispositivos médicos y/o medicamentos en Latinoamérica.
- Haber liderado proyectos que incluyan las regiones Andina, Centroamérica o Colombia.

**Additional information**:

**Overview**
At the heart of QIAGEN’s business is a vision to make improvements in life possible.

We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe.
Our most valuable asset are our employees - more than 6000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us.
There are few players who have shaped the world of modern science and healthcare as much as QIAGEN, and we have only just started.
If you are looking to advance your career, are seeking new challenges and opportunities, enjoy working in dynamic, international and diverse teams and want to make a real impact on people’s lives, then QIAGEN is where you need to be.

Join us. At QIAGEN, you make a difference every day.
**Position Description**
We are looking for an experienced and motivated Regulatory Affairs (RA) Manager to lead and undertake regulatory responsibility for Mexico and Central Americas (CAR) to ensure our IVD products comply with regional regulations and laws. The CAR RA Manager will report to Sr Director Regulatory Affairs International Program and will partner closely with the RA Manager for Brazil and South America, QIAGEN Franchise RA Directors, Managers, Franchise and Regional Leads to develop and execute effective regulatory strategies to deliver new products to the LATAM region with a responsibility for Mexico and Central America. This role also involves evaluating changes and maintaining existing product licenses.

The CAR RA manager will have direct line management responsibilities for a small team to execute strategy and registrations in accordance with business needs.

**Key Responsibilities**
- **Regulatory Strategy Development**:

- Develop and implement regulatory strategies to facilitate product approvals, registrations, and commercialization for Central Americas.
- Assess regulatory risks and advise senior management on strategies to achieve regulatory objectives.
- **Regulatory Submissions and Compliance**:

- Is responsible for the preparation, review, and submission of compliant regulatory documents to Regulatory agencies or Commercial Partners for successful product approvals and licenses.
- Provides regulatory impact assessments for product/process/supplier changes
- Independently makes decisions regarding work and operational plans and schedules to deliver RA functional and business goals for CAR.
- **Liaison with Regulatory Agencies**:

- Serve as the primary contact for communication with regulatory agencies for Direct Markets and/commercial partners for distributor markets.
- Represent the company in regulatory meetings and negotiations.
- **Cross-Functional Collaboration**:

- Work with teams across the organization, including R&D, quality assurance, manufacturing, marketing, and legal departments.
- Provide regulatory guidance and support to internal stakeholders.
- Provides leadership and mentoring to direct reports, including goal setting, prioritization support and professional development and performance management.
- Assists in the development of best practices for Regulatory Affairs International Program to maintain and establish efficient processes
- **Regulatory Compliance Training and Education**:

- Develop and deliver training programs on regulatory requirements and best practices.
- Ensure employees are equipped with the knowledge to maintain compliance.
- **Regulatory Intelligence and Advocacy**:

- Monitor changes in regulations and industry standards.
- Conducts regulatory intelligence activities and advocate for the company’s interests.

**Position Requirements**
- Bachelor’s or Master’s degree in a relevant field such as Science, Engineering, Pharmacy, or Life Sciences.
- Minimum 5 years (5+) regulatory affairs experience in a medical device or vitro-diagnostic industry for Mexico and the Central Americas region.
- Demonstrated knowledge and understanding of medical device regulations and delivery or co-ordination of successful medical device license approvals in Mexico, and Central America (Costa Rica, El Salvador, Guatemala, Honduras, Panama, Nicaragua, Belize).
- **Fluent in Spanish and Professional Proficiency in English.**:

- Experience and understanding of regional regulatory requirements for medical devices, IVDs and CDx products. Familiar with processes and interactions with agencies in Central Americas.
- Experience of MD/IVDs/CDx requirements for Mexico and key CAR markets.

**Please send your CV in English!**
**What we offer**
At the heart of QIAGEN are our people who drive our success. We act with passion, always challenging the status quo to drive innovation and continuous improvement. We inspire with our leadership and make an

Moody's is a global integrated risk assessment firm that empowers organizations to make better decisions.

Moody’s is seeking an experienced AVP Compliance and Regulatory Officer to support the Moody’s Local rating businesses in Latin America, with a particular focus on Mexico. Based in Mexico City, this role will be part of the ML Compliance and Regulatory Affairs team within Moody’s Global Compliance and report to the Head of Compliance and Regulatory Affairs for Moody’s Local in New York.
- The AVP Compliance and Regulatory Officer will be the chief point of contact to support the Moody’s Local businesses in identifying and navigating regulatory and reputational risks and opportunities in Mexico and other jurisdictions to be specified. Responsibilities include:

- Coordinate compliance and regulatory affairs efforts in Mexico and other jurisdictions to be specified in alignment with Moody’s Local regional standards, ensure Moody's Local entities are meeting domestic regulatory requirements, and facilitate escalation and appropriate resolution of compliance and regulatory issues.
- Act as the designated compliance officer and primary liaison with regulators in Mexico and other jurisdictions to be specified, respond to supervisory inquiries, prepare all periodic compliance reports, and prepare internal staff for regulatory examinations.
- Identify, analyse and report policy and regulatory developments that could affect the Moody’s Local businesses in each relevant jurisdiction, contribute to the drafting of responses to consultation papers and other policy-related submissions, and manage any regulatory change.
- Support the successful development and implementation of codes of conduct, compliance policies and procedures in alignment with Moody’s Local regional standards, and advise employees on their implementation, including with respect to securities trading, gifts, outside business interests, confidentially, separation, recordkeeping and regulatory disclosures.
- Contribute as necessary to the drafting of talking points and briefing packages for meetings with regulators, government bodies and standard setters to advocate for ML’s policy positions and in support of strategic projects.
- Support the compliance surveillance and investigations team where necessary.
- Assist in the preparation and delivery of training materials and presentations as necessary.
- Carry out compliance risk assessments and identify actions that the company must take to mitigate those risks.
- Report to the Moody’s Local boards of directors and senior management on a periodic and ad hoc basis.
- Assist in other compliance and regulatory affairs tasks as required to ensure team objectives are achieved.

Qualifications:

- 5-8 years of compliance and/or regulatory affairs experience at a financial industry regulator or regulated financial services firm.
- Bachelor's degree or higher in business, law or other finance related discipline.
- Proven ability to lead meetings with financial regulators and senior executives in a multinational corporation.
- Strong written and oral communication skills; fluent in English and Spanish, both verbal and written.
- Professional, pro-active, flexible, diligent and dependable.
- Excellent interpersonal skills and team oriented.
- Must be highly organized with attention to detail and the ability to multi-task and meet tight deadlines.
- Ability to adapt to changing business and regulatory environments.
- Must be able to work on own initiatives, with limited supervision.
- Unquestionable personal code of ethics, integrity, inclusion and trust.
- Wiliness to travel as needed to the different countries in which Moody’s Local operates to meet with regulators and other external stakeholders.
- Strong Microsoft Excel, PowerPoint, and Word skills.

Moody's is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation, gender expression, gender identity or any other characteristic protected by law.

For more information on the Securities Trading Program, please refer to the STP Quick Reference guide on ComplianceNet

Unilever is currently hiring for Regulatory Affairs Manager Foods Mexico

Function : Regulatory Affairs (R&D)

Scope: Local

Location: Bosques, Mexico

Terms & Conditions: Full time. Office-based role

ABOUT UNILEVER

With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people – we believe that when our people work with purpose, we will create a better business and a better world.

At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don’t believe in the ‘one size fits all’ approach and instead we will equip you with the tools you need to shape your own future.

Unilever Foods is a 13+ Billion Euro business representing 22% of Unilever’s TO, of which Mexico is one of the key markets. Unilever Foods business is focussed on 3 attractive global verticals: condiments, cooking aids and mini-meals and Unilever Food Solutions.

We are seeking a highly motivated and experienced Regulatory Affairs Manager Foods Mexico, to join our Foods RA team in Latam, a dedicated BU part of BG-led markets organisation. This role is crucial to provide regulatory input in innovation projects, ensure that our products comply with all relevant local regulations and standards, and support the Foods RA team in the Latam regulatory advocacy agenda.

JOB PURPOSE

Find your purpose at Unilever. You will lead innovations, big and small, that will make our business win and grow. You will learn from brilliant business leaders and colleagues in a truly global and diverse culture to ultimately become a better you.

The Manager for Foods Regulatory Affairs will be responsible for managing regulatory compliance and innovation partnering for our Foods portfolio in Mexico. This includes ensuring that all products meet country regulatory requirements, supporting product development and innovation, and providing regulatory guidance to cross-functional teams. It also includes representing Unilever in the food trade association, to monitor regulatory changes and influence on key priorities for Foods business.

KEY RESPONSABILITIES

• Advocacy: Shaping future regulatory space

• Build technical influencing strategies for Unilever positions

• Collaborate with NPD (R&D), Legal, External Affairs, and other key functions to define consistent, aligned views and positions

• Represent Unilever in relevant trade associations

• Manage if needed key contacts with Authorities on priority regulatory topics for the business

• Innovation: Knowledge of Mexican food regulations to guide new development

• Provides local regulatory input to the innovation projects

• Coordinates the local regulatory strategy, organization and guidance for the implementation of innovation projects in Mexico

• Compliance: Maintain continuous regulatory compliance of Mexican food portfolio

• Coordinates regulatory compliance of product formulations and technical claims with Mexican regulations

• Facilitate product registrations and government certifications, understanding specific market requirements set by the Authorities

• Prepare and review technical documentation to support the registration process

• Collaborate with Legal, NPD, and other teams to ensure alignment on compliance matters

• Issue management: ensure regulatory support in case of issues

REQUIRED QUALIFICATIONS

• A bachelor’s or master’s degree in a relevant scientific field

• Over 6 years of regulatory affairs experience in foods and beverages.

• Proven experience in product registrations and government certifications.

• Experience working in cross-functional teams within a matrix environment, both face-to-face and virtually.

Skills

• Strong knowledge of food regulations and standards in Mexico and Latam

• Experience in regulatory interpretation.

• Excellent communication (technical communication skills) and interpersonal skills.

• Strong analytical and problem-solving skills.

• Ability to work independently and as part of a team.

• Digital dexterity

Key interfaces:

• R&D/ product development and innovation teams, including BU R&D leaders

• Legal, External affairs/Coms and QA

• Regional and local business teams

• Global and Latam RA network

Leadership

• You are an inclusive motivator of people. Your team deliver with real passion, growing and learning from each other whilst delivering quick wins.

• You are still responsible for your own results and as a manager, you also need to motivate others to deliver with passion, creating an inclusive and engaging climate around you. You can balance challenge with support and coaching. You understand the wider business context and you are emotionally intelligent enough to motivate people to deliver what is needed.

Unilever is an organisation committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bringing their ‘Whole Self’ to work and this includes you! Thus if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.

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