Generics [U.K.] Ltd. Posted July 9, 2026

Artwork Coordinator

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.

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

Support Viatris's mission by conducting artwork coordination / operations, ensuring the correct artwork is implemented on time and in compliance with Competent Authority and Business requirements. Responsible for coordinating the creation, approval and implementation of market artwork within Viatris's Global Change Management System and documented Business Processes, acting as the key interface between Regulatory, Packaging Sites, Artwork Studios and Supply Chain. Role is an individual contributor.

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

Process new artwork requests in a timely manner, prioritising in accordance with any due dates for creation or implementation (Competent Authority or Business Commitments).

Collate and create accurate design briefs and instructions for artwork studios, in collaboration with Regulatory, Packaging Site and Commercial requirements / instructions.

Perform design checks on artwork to ensure compliance with design brief / instructions and national guidelines.

Ensure artwork reviews and checks (content and technical) have been performed by all relevant departments before releasing AW for implementation, including collating and requesting amendments to artwork identified during the approval process. Where required and according to Packaging Site requirements, review and approve Production Print Proofs.

Confirm and Communicate implementation instructions to the packing site, including invalidation instructions for superseded artwork.

Coordinate Artwork Requests within the Global Change Management Artwork Systems and any related data bases, ensuring correct documentation has been completed and uploaded.

Create SKU records for New Product Launches and maintain existing SKU records where already available.

Provide support with any identified artwork queries / risks / issues, escalating to Artwork Supervisor and / or Artwork Compliance Manager where necessary.

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:

Experience in pharmaceutical or FMCG artwork coordination is desirable

Associate’s degree or university diploma (or equivalent)

Proven experience in coordination and project management

Knowledge of pharmaceutical artwork coordination is advantageous

Ability to manage multiple priorities and meet tight deadlines

Strong attention to detail with excellent organisational skills

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 Team Lead
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.