Mylan, Lda. Posted November 11, 2026

Labeling Hub Manager

Lisbon, Portugal Full time
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Mylan, Lda. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Mylan, Lda.

Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on number of award lists that demonstrate the impact we are making.

This posting supports ongoing hiring needs and may be used to consider candidates for upcoming opportunities.

Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on a number of award lists that demonstrate the impact we are making.

Every day, we rise to the challenge to make a difference, and here’s how the Labeling Hub Manager role will make an impact:

By ensuring compliant and timely implementation of labeling updates across assigned countries and serving as a trusted subject matter expert to support regional and global stakeholders on labeling-related initiatives.

Key Point of Contact to Global Labelling Team regarding countries/licenses under her/his responsibility

Communicate clearly issues and resolutions to peers and subordinates in a meaningful way.

Ensure local labelling text is prepared right first time and on-time according to agreed company procedures and objectives.

Support regional labelling team members with health authority questions, requests for further information, preparation, and review of labelling documents prior to submission.

Advise her Labelling Hub Manager regarding any deficiencies or issues.

Ensure that supportive documents, not limited to Core Data Sheet or other Reference Label such as USPI, SmPC are obtained in a timely manner to the countries according to local legislation

Arranges and updates Local Labelling texts above market on behalf of all impacted markets to ensure their conformity with internal procedures and local legislation.

Manage all labelling variations through the Regulatory Information Management System and Trackwise Change control environment as needed to show compliance to global submission timelines and valid reason for delay.

Liaise with Translation vendors as needed.

General knowledge of preparing artwork from labelling text and the interface with Launch Management, Supply Chain and Quality teams.

Ensures maintenance of relevant systems according to relevant SOPs.

Ensures compliance with all relevant company SOPs

Provide support during Medical and Regulatory Audits.

The minimum qualifications for this role are:

Bachelor's degree in Science, Medicine or Pharmacy, or another related field

Labelling and Regulatory experience

Regulatory experience working with Regional Heath Authorities and in-depth Regional Labelling knowledge

Highly developed interpersonal, presentation and communication skills with advanced English language capability

Ability to provide innovative approaches/recommendations to product labelling that meet corporate goals while maintaining compliance with relevant laws and regulations.

Understand GLC requirements/ processes and EU/ US regulatory requirements.

The ability to influence effectively in a matrixed, cross functional team environment

At Viatris, we are dedicated to building a truly diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.

Why Viatris?

At Viatris, we offer competitive salaries, benefits, and an inclusive environment where you can use your experiences, perspectives, and skills to help make an impact on the lives of others. You will also have the opportunity to access excellent career progression opportunities and work-life balance initiatives.

Diversity & Inclusion at Viatris

At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare, not as it is, but as it should be. If you would like to know more about what diversity, equity, and inclusion means to us, please visit  https://www.viatris.com/en/Careers/Diversity-and-Inclusion

Sustainability at Viatris

Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit  https://www.viatris.com/en/about-us/corporate-responsibility

A t Viatris, we offer   competitive   salar ies , benefits   and   an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.

Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Lisbon, Portugal
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 234 comparable Manager Regulatory Affairs roles across 73 biopharma companies.

234Comparable roles tracked
215Currently active
73Companies hiring similar roles
29Countries represented

Salary context

69 of 234 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Manager, Global Regulatory Strategy · Sarepta Therapeutics, Inc. $116,000/yr – $145,000/yr
Peer group range $130,500 – $236,300 (median $180,500)

Where these roles are based

Top locations among the 234 comparable roles

United States103
India26
United Kingdom20
Japan17
Ireland10
China7

+ 23 more countries

Seniority mix

234 of 234 peers have a known seniority level

Manager171
Associate Director52
Associate11

Therapeutic area mix

20 of 234 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology7
Oncology6
Ophthalmology4
Dermatology & Aesthetics1
Rare Disease1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Mylan, Lda. Lisbon, Portugal Manager
Same function Same seniority Same country
60%similar
Mylan, Lda. Lisbon, Portugal Manager
Same function Same seniority Same country
60%similar
Amgen Capability Center Portugal Ltda Lisbon, Portugal Manager
Same function Same seniority Same country
60%similar
Mylan, Lda. Lisbon, Portugal Manager
Same function Same seniority Same country
50%similar
Mylan, Lda. Lisbon, Portugal Associate
Same function Adjacent seniority Same country
45%similar
Gilead Sciences K.K. Tokyo, Japan Manager
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Regulatory Affairs job in Portugal, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Senior Labeling Hub Manager
Mylan, Lda. · Lisbon, Portugal · Manager
Function Therapeutic area Seniority Country
60%
Regulatory Affairs Manager - Central Regulatory Affairs (CRA), Europe
Mylan, Lda. · Lisbon, Portugal · Manager
Function Therapeutic area Seniority Country
45%
Senior Regulatory Affairs Manager
Gilead Sciences K.K. · Tokyo, Japan · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Global Patient Safety
Regeneron Japan KK · Tokyo, Japan · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.