Roche Posted October 23, 2026

Regulatory Affairs Specialist

Prishtina, Pristina, Kosovo FULL_TIME
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Roche 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

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

I. Summary of Main Responsibilities:

Ensure that all Product Licenses in Kosovo are always fully up-to-date and compliant.

Responsible for ensuring that all regulatory documentation is effectively managed and that all regulatory submissions and approvals are accurately documented within relevant systems and databases.

Ensure that progress of applications and changes to registered details are communicated to local and global stakeholders, as appropriate, with minimum delay.

Interact and negotiate with local HAs and internal stakeholders to build and cultivate trusted partnerships and achieve successful regulatory outcomes.

Take active participation in shaping the policy environment.

Develop and manage effective working relationship with the regulators in Kosovo, Roche International Regulatory and other key customers.

Maintain a level of knowledge of local and international regulatory legislation and awareness of changes within the regulatory environment.

Ensure the timely communication on changes in local (Kosovo) regulations to Roche Global and to the local stakeholders in accordance with Roche requirements.

As assigned, gather and disseminate regulatory intelligence within the Affiliate.

Ensure regulatory filings are aligned with commercial and supply needs to assure business continuity and provide Regulatory Affairs input into relevant cross-functional Affiliate business strategies

Develop innovative, risk-based regulatory strategies and work plans for assigned products or business areas within the Affiliate to accelerate access of medicines to patients.

Builds strong relationships and ensures good collaboration and communication between LTO and other affiliate, regional and global functions.

Support regulatory audit/ inspection-readiness for the Affiliate, including leading or participating in internal/external regulatory audits.

Ensure assigned Affiliate activities comply with Roche global standards and local regulations.

Prepares and maintains product information for regional make-up in line with the reference label, and partners with global labelling, artworks, supply chain and affiliates to ensure implementation of packaging components within agreed company timelines.

Prepares packaging components (primary, secondary and product leaflet) in alignment with reference label through the lifecycle maintenance

Works in close collaboration with global stakeholders (e.g. supply, artworks, Pharma technical) and affiliates to ensure efficient workflows with functions involved in the labelling processes.

II. Competencies:

High degree of proficiency in Albanian and English language.

Strong verbal and written communication skills.

Analytical and problem solving skills.

Ability to work as part of a team.

Excellent listening and decision-making skills.

Well-organized, detail oriented professional and ability to prioritize and make decisions.

Highly self-motivated; able to lead initiatives with authority.

III. Experience, Skills, Knowledge:

Location: Based in Kosovo or North Macedonia.

University education – pharmacist

Experience in the pharmaceutical industry and in a regulatory environment.

Excellent understanding of the pharmaceutical industry, drug development environment.

Extensive knowledge of relevant regulations and ability to evaluate the impact of those regulations within the external and internal environment.

Commitment to deliver high quality output, even under pressures sometimes demanded by regulatory deadlines

This role is a 12-months temporary cover for maternity leave.

 

 

Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Prishtina. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Prishtina, Pristina, Kosovo
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 589 comparable Regulatory Affairs roles across 115 biopharma companies.

589Comparable roles tracked
544Currently active
115Companies hiring similar roles
54Countries represented

Salary context

157 of 589 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 · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $75,038 – $380,750 (median $186,375)

Where these roles are based

Top locations among the 589 comparable roles

United States236
India47
Japan34
United Kingdom33
Poland27
Ireland20

+ 48 more countries

Seniority mix

456 of 589 peers have a known seniority level

Manager181
Director73
Senior59
Associate Director55
Intern/Fellow/Postdoc25
Senior Director23
Principal17
Associate13
Executive/VP10

Therapeutic area mix

44 of 589 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology14
Immunology10
Rare Disease6
Dermatology & Aesthetics5
Vaccines & Infectious Disease3
Neuroscience3
Cardiovascular / CVRM2
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.

25%similar
Lilly Shanghai, Shanghai, China Associate Director
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Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie Maidenhead, ENGLAND Manager
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Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie Mettawa, IL Associate Director
Same function

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

25%similar
AbbVie Director
Same function

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

Open in 3 locations

North Chicago, United StatesFlorham Park, United StatesWaltham, United States
25%similar
AbbVie Associate Director
Same function

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Open in 2 locations

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Notify me about similar jobs

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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.

25%
Regulatory Affairs Associate Director
Lilly · Shanghai, Shanghai, China · Associate Director
Function Therapeutic area Seniority Country
25%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
25%
Director, RA Global Regulatory Strategy
AbbVie · Florham Park, NJ · Director
Function Therapeutic area Seniority Country
25%
Associate Director, Regulatory Affairs US & Canada Strategy Lead – Facial Aesthetics - Device
AbbVie · North Chicago, 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.