Generics [U.K.] Ltd. Posted July 13, 2026

Artwork Team Lead

Lisbon, Portugal Full time
Regulatory Affairs

Generics [U.K.] Ltd. 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

Generics [U.K.] Ltd.

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.

Support Viatris’s mission by leading artwork coordination and operations to ensure accurate, compliant, and timely implementation of artwork across designated regional cluster markets.

This role is responsible and accountable for managing the end-to-end process, from creation and approval to implementation, within Viatris’s Global Change Management System and established Business Processes.

Serving as the primary interface between Regulatory, Quality, Project Management, Supply Chain, Packaging Sites, and Artwork Studios, driving collaboration and operational excellence across all stakeholders. The role also carries people management responsibilities..

Every day, we rise to the challenge to make a difference and here’s how the Artwork Team Lead role will make an impact:

Serve as the primary escalation point for artwork coordinators across cluster markets, providing tactical oversight and guidance

Lead project management for cluster market initiatives, ensuring timely execution and strong support for local and regional teams

Manage operational production artwork task volumes across the team, balancing regulatory compliance with commercial priorities.

Review artwork request queues to maintain visibility of workload and allocate tasks equitably based on capacity, expertise, and priority

Build deep market knowledge and translate learnings into process and system improvements

Coordinate artwork requests within the Global Change Management System, ensuring accurate documentation

Create and maintain SKU records for new launches and existing products

Resolve artwork queries and risks proactively, escalating to Artwork Leadership or Compliance when needed

Lead a high-performing, engaged team, embedding compliance, driving development, and supporting succession planning

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:

Bachelor’s degree or equivalent qualification

Experience in pharmaceutical artwork development and review

Strong coordination and project management skills

Solid understanding of local regulatory requirements related to artwork

Advanced proficiency in Microsoft Excel, including pivot tables and data visualisation

Proven ability in data analysis and reporting

Demonstrated experience in training, mentoring, and managing team members

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.

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
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 305 comparable Regulatory Affairs roles across 67 biopharma companies.

305Comparable roles tracked
275Currently active
67Companies hiring similar roles
37Countries represented

Salary context

85 of 305 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
Highest disclosed · AVP, Therapeutic Area Head, Clinical Safety and Risk Management · Merck $378,100/yr – $595,100/yr
Peer group range $98,050 – $486,600 (median $205,000)

Where these roles are based

Top locations among the 305 comparable roles

United States124
Ireland25
India25
United Kingdom17
Poland16
Japan13

+ 31 more countries

Seniority mix

261 of 305 peers have a known seniority level

Manager112
Director61
Senior27
Associate Director26
Senior Director12
Executive/VP11
Associate8
Principal2
Intern/Fellow/Postdoc2

Therapeutic area mix

33 of 305 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology10
Dermatology & Aesthetics6
Neuroscience6
Immunology4
Cardiovascular / CVRM2
Rare Disease2
Respiratory2
Vaccines & Infectious Disease1

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
Generics [U.K.] Ltd. Lisbon, Portugal
Same function Same country
40%similar
Bayer Carnaxide, Portugal
Same function Same country
25%similar
Lilly Indianapolis, Indiana, United States of America
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Shanghai, Shanghai, China Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Bracknell, United Kingdom Principal
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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%
Artwork Coordinator
Generics [U.K.] Ltd. · Lisbon, Portugal · Seniority not listed
Function Therapeutic area Seniority Country
25%
Sr Regulatory Affairs Manager- DIA
Lilly · Shanghai, Shanghai, China · Manager
Function Therapeutic area Seniority Country
25%
Associate Director/Director, GRA, Regulatory Affairs Head – Canada
Lilly · Ontario, Ontario, Canada · Associate Director
Function Therapeutic area Seniority Country
25%
Sr.Manager- Regulatory Delivery Excellence, China Regulatory Affairs
Lilly · Shanghai, Shanghai, China · 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.