Teva Pharmaceuticals Posted June 19, 2026

Regulatory Artwork Administrator Markets (Temporary)

Sofia, Bulgaria Type not listed
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Teva Pharmaceuticals 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

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

How you’ll spend your day

Artwork Lifecycle Management:

Initiate new or revised artwork requests in Teva’s internal system (TevaArt)

Verify artwork requests and associated documentation for completeness and accuracy

Review artwork files using verification tools, checklists, and country-specific requirements

Coordinate corrections and feedback with artwork studios and market teams

Approve final artwork files and assign final light approval tasks to markets before blueprint creation

Communication & Coordination:

Manage requests from markets and provide timely status updates

Collaborate with Regulatory Affairs functions and other internal stakeholders

Compliance & Quality:

Ensure adherence to internal procedures and external regulatory guidelines

Maintain high standards of accuracy and quality under pressure

Your experience and qualifications

High school or university degree in Pharmacy or life science is preferred

Previous experience in a coordination role or within the pharmaceutical, healthcare, or food industry will beconsidered as an advantage

Advanced English proficiency (additional languages are a plus)

Strong organizational and communication skills

Proficiency in Microsoft 365 and experience with databases/document management systems

Ability to manage multiple projects and deadlines in a fast-paced environment

Strong interpersonal skills and attention to detail

Ability to reprioritize tasks and maintain quality under pressure

How We’ll Take Care of You

Dynamic and challenging work environment in one of the world leading pharmaceutical company and thebiggest pharmaceutical company in Bulgaria

Competitive remuneration bound with performance

Additional healthcare insurance

Transportation allowance and other flexible benefits

Option to work from home as per the company policy

Opportunity for development

Make a difference with Teva Pharmaceuticals

If this sounds like the right opportunity for you, send us your CV in English.

Already Working @Teva?

Make sure to apply through our internal career site on Twist, your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Sofia, Bulgaria
Employment type
Not listed

How this role compares

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

We currently track 397 comparable Regulatory Affairs roles across 88 biopharma companies.

397Comparable roles tracked
385Currently active
88Companies hiring similar roles
45Countries represented

Salary context

122 of 397 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
Lowest disclosed · Associate Manager CMC Regulatory Compliance · Merck KGaA $77,800/yr – $116,700/yr
Highest disclosed · AVP, Therapeutic Area Head, Clinical Safety and Risk Management · Merck $378,100/yr – $595,100/yr
Peer group range $97,250 – $486,600 (median $186,375)

Where these roles are based

Top locations among the 397 comparable roles

United States171
India28
United Kingdom27
Japan23
Ireland21
Poland20

+ 39 more countries

Seniority mix

318 of 397 peers have a known seniority level

Manager137
Director64
Associate Director40
Senior36
Senior Director15
Executive/VP13
Associate8
Intern/Fellow/Postdoc3
Principal2

Therapeutic area mix

33 of 397 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology15
Neuroscience6
Dermatology & Aesthetics3
Rare Disease3
Immunology3
Cardiovascular / CVRM2
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
Teva Pharmaceuticals Sofia, Bulgaria Associate
Same function Same country
40%similar
Teva Pharmaceuticals Sofia, Bulgaria
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 Indianapolis, Indiana, United States of America Senior Director
Same function

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

25%similar
Lilly Ontario, Ontario, Canada Associate Director
Same function

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

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%
Regulatory Affairs Associate (CMC Lifecycle)
Teva Pharmaceuticals · Sofia, Bulgaria · Associate
Function Therapeutic area Seniority Country
25%
Sr Regulatory Affairs Manager- DIA
Lilly · Shanghai, Shanghai, China · Manager
Function Therapeutic area Seniority Country
25%
Regulatory Affairs Associate Director
Lilly · Shanghai, Shanghai, China · Associate Director
Function Therapeutic area Seniority Country
25%
Associate Director, Regulatory Affairs Advertising & Promotion - Digital & Corporate Communications
AbbVie · Mettawa, IL · Associate Director
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.