Mylan, Lda. Posted September 23, 2026

Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe

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.

Our Story

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via :

Access – Providing high quality trusted medicines regardless of geography or circumstance;

Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and

Partnership – Leveraging our collective expertise to connect people to products and services.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.

For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.

The Role & What You Will Be Doing

This is an exciting opportunity for an experienced Regulatory Affairs professional to play a key role in managing regulatory activities across Europe. You will work with cross-functional teams, affiliate partners, and health authorities to support product registrations, lifecycle management, and regulatory compliance.

Every day, we rise to the challenge to make a difference, and here’s how the Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe role will make an impact:

Key responsibilities for this role include:

Manage regulatory activities for a portfolio of pharmaceutical products across Europe.

Prepare and submit regulatory applications, variations, renewals, and other lifecycle management activities.

Support new product registrations through European and national regulatory procedures.

Collaborate with European affiliate teams to ensure successful implementation of regulatory strategies.

Maintain regulatory databases and documentation to ensure ongoing compliance.

Build strong relationships with internal stakeholders and external business partners.

Support interactions with regulatory authorities and contribute to responses to health authority queries.

Monitor regulatory developments and assess their impact on the product portfolio

About Your Skills & Experience

For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:

A degree in Pharmacy, Biotechnology, Life Sciences, or a related scientific discipline.

2-3 years of Regulatory Affairs experience within the pharmaceutical industry.

Knowledge of European regulatory procedures and post-approval lifecycle management.

A Master's qualification in Regulatory Affairs would be advantageous.

Strong communication and stakeholder management skills.

Excellent organisational skills and attention to detail.

Fluent English, both written and spoken.

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.

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
Not listed
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 407 comparable Regulatory Affairs roles across 100 biopharma companies.

407Comparable roles tracked
394Currently active
100Companies hiring similar roles
43Countries represented

Salary context

116 of 407 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Peer group range $115,000 – $380,750 (median $205,000)

Where these roles are based

Top locations among the 407 comparable roles

United States165
India34
Japan28
United Kingdom25
Poland21
Ireland20

+ 37 more countries

Seniority mix

332 of 407 peers have a known seniority level

Manager128
Director64
Associate Director43
Senior38
Intern/Fellow/Postdoc19
Senior Director16
Executive/VP12
Associate9
Principal3

Therapeutic area mix

38 of 407 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology18
Rare Disease7
Immunology4
Vaccines & Infectious Disease3
Dermatology & Aesthetics2
Neuroscience2
Cardiovascular / CVRM2

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.

40%similar
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Mylan, Lda. Lisbon, Portugal Senior
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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.

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.

40%
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Function Therapeutic area Seniority Country
40%
Senior Specialist Regulatory Operations (Electronic Submissions)
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Function Therapeutic area Seniority Country
40%
Associate Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe
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Function Therapeutic area Seniority Country
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Senior Regulatory Affairs Administrator - Central Regulatory Affairs (CRA)
Mylan, Lda. · Lisbon, Portugal · Senior
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.