Jobs › Companies › Haleon › Regulatory Affairs Manager

À propos de ce poste Regulatory Affairs Manager chez Haleon

Haleon · Sur site · Mexico City Artz Pedregal Flex

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.

Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.

Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

As Regulatory Affairs Manager, you will be responsible for designing and implementing regulatory strategies that support business growth, innovation, and product lifecycle management in Mexico. You will work closely with local, regional, and global stakeholders to secure timely regulatory approvals, ensure compliance with applicable regulations, and represent the company before regulatory authorities and industry associations.


This role will provide YOU the opportunity to lead key activities to progress YOUR career, including:

  • Develop and implement regulatory strategies for product registrations, variations, renewals, and lifecycle management activities in Mexico.
  • Ensure timely regulatory approvals that support innovation, line extensions, and business objectives.
  • Prepare, review, and submit regulatory dossiers and responses to Mexican Regulatory Authorities.
  • Monitor and assess changes in local regulatory requirements, ensuring ongoing compliance with applicable legislation and company policies.
  • Partner closely with Commercial, Marketing, Trade Marketing, Supply Chain, Quality, and Sales teams to support product development and commercialization plans.
  • Represent the company in interactions, negotiations, and communications with regulatory authorities.
  • Conduct regulatory risk assessments and provide strategic recommendations to senior leadership.
  • Support manufacturing site inspections and activities related to obtaining required regulatory certifications, where applicable.
  • Provide regulatory oversight for clinical and bioequivalence studies, where applicable.
  • Review and approve promotional materials requiring regulatory authorization while ensuring compliance with local regulations and corporate policies.
  • Drive continuous improvement initiatives to enhance efficiency, productivity, and effectiveness within the regulatory organization.
  • Maintain accurate regulatory documentation, submissions, and correspondence.
  • Build strong external partnerships with industry associations and regulatory stakeholders to help shape the external regulatory environment.
  • Lead, coach, and develop members of the regulatory team, fostering growth and capability building.
  • Navigate complex regional and global matrix environments to deliver business results.

Why You?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • Bachelor’s degree in a scientific discipline such as Pharmacy, Chemistry, Medicine, or a related field.
  • 5+ years of experience as a Regulatory Affairs Manager.
  • Strong experience within global consumer healthcare, pharmaceutical, or related industries.
  • Demonstrated knowledge of Mexican regulatory requirements and regulatory submission processes.
  • Experience supporting product lifecycle management, registrations, variations, and renewals.
  • Excellent verbal and written communication skills in both English and Spanish.
  • Experience managing and developing people and teams.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Strong scientific evaluation, interpretation, and communication skills.
  • Experience managing broad portfolios including medicines and medical devices.
  • Strong project management capabilities.
  • Proven ability to influence stakeholders across complex matrix organizations.
  • Creative, innovative, and solution-oriented mindset.
  • Strong business acumen and results orientation.
  • Ability to assess and manage regulatory risks effectively.
  • Experience working directly with regulatory authorities and trade associations.
  • Strong interpersonal skills with the ability to build trust and collaborative relationships.
  • High sense of urgency, attention to detail, and ability to work independently

 

 

 

 Job Posting End Date

 

 

2026-11-03

 

 

 

Equal Opportunities

Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that Haleon is a place where all our employees feel they truly belong.

During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. 

The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.

 

 

 

Adjustment or Accommodations Request

If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We’ll provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence. 

 

 

 

Note to candidates

The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.

Prêt à postuler chez Haleon ?
Postuler chez Haleon

À propos de Haleon

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver bette

Voir tous les emplois chez Haleon →

Emplois similaires

Parexel
Senior Regulatory Affairs Associate- Clinical Trial Application
Parexel
⚡ Postuler tôt India-Bengaluru-Remote · lieu restreint
● Nouveau 👁 Vu ✓ Postulé il y a 1 h
IQVIA
Associate Program Director, Regulatory Affairs
IQVIA
⚡ Postuler tôt Bucuresti, Romania Sur site
● Nouveau 👁 Vu ✓ Postulé il y a 2 h
IQVIA
Associate Program Director, Regulatory Affairs
IQVIA
⚡ Postuler tôt Budapest, Hungary Sur site
● Nouveau 👁 Vu ✓ Postulé il y a 2 h
Johnson & Johnson
Manager, APAC, Regulatory Affairs, Oncology
Johnson & Johnson
⚡ Postuler tôt Singapore, Singapore Sur site
● Nouveau 👁 Vu ✓ Postulé il y a 10 h
Siemens Healthineers
Specialist/Senior Specialist, Regulatory Affairs
Siemens Healthineers
⚡ Postuler tôt SEL AC Sur site
● Nouveau 👁 Vu ✓ Postulé il y a 10 h
FreedomCare
Regulatory Affairs Associate (Denver, CO - Field - Based)
FreedomCare
⚡ Postuler tôt Denver, CO Sur site $80,000–$90,000
● Nouveau 👁 Vu ✓ Postulé il y a 11 h
Braveheart Bio
Senior Manager, Regulatory Affairs
Braveheart Bio
⚡ Postuler tôt San Francisco, CA or Remote or... Hybride $170,000–$195,000
● Nouveau 👁 Vu ✓ Postulé il y a 13 h
Flamingo
Regulatory Affairs Manager
Flamingo
⚡ Postuler tôt New York, NY Sur site $120,000–$150,000
● Nouveau 👁 Vu ✓ Postulé il y a 21 h
Lume Deodorant
Regulatory Affairs Manager
Lume Deodorant
⚡ Postuler tôt New York, NY Sur site $120,000–$150,000
● Nouveau 👁 Vu ✓ Postulé il y a 21 h

Inscrivez-vous pour des suggestions adaptées aux emplois que vous ouvrez et aux recherches que vous enregistrez.

Plus d’emplois chez Haleon

Voir tous les emplois chez Haleon →

Postuler maintenant
🤖

Doucement — un instant

JobsRadar a été conçu pour de vraies personnes qui traversent une période difficile dans leur recherche d’emploi — pas pour des requêtes automatisées. Vous cliquez beaucoup trop vite et vous êtes maintenant temporairement bloqué.

Revenez plus tard. Si vous cherchez réellement un emploi, nous sommes de votre côté — agissez simplement comme un être humain.

Catch your next role the second it’s posted.

Create a free account and we’ll watch the boards for you — the instant a job matches your search, it lands in your inbox or Telegram. No digging, no refreshing.

Create free account

Free forever · takes 30 seconds · already have one?

Prenez une longueur d’avance dans votre recherche d’emploi.

Rejoignez notre canal Telegram pour ce qui vous aide à décrocher le poste — références salariales, le pouls hebdomadaire du marché et les annonces de nouveautés. Pas de spam, que du signal.

Rejoindre le canal — c’est gratuit