Who We Are

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Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$6 billion. Supported by more than 40 manufacturing facilities and more than 40.000 employees around the globe, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe.
Over the last two decades, Sun Pharma has established itself as a leading player in the generics market, and are rapidly ramping up their presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology.
Values

At Sun Pharma our core values—Humility, Integrity, Passion, and Innovation—are part of our unique culture, known as Sunology.

We are empowering our employees to create their “Own Sunshine”. We believe in being Better Everyday by investing on lifelong learning, Taking Charge by owning our impact, and Thriving Together in a workplace where collaboration is encouraged. We are committed to being an inclusive and equitable employer, valuing diverse perspectives and creating an environment where all individuals feel respected, heard, and inspired to bring their best selves to work.

Role Overview

We are seeking a motivated

Regulatory Affairs Artwork Specialist

with 1–2 years of experience in a multinational pharmaceutical environment. The ideal candidate will have hands-on expertise in packaging materials creation and lifecycle management, supporting regulatory activities for medicinal products in Italy.

Key Responsibilities

The selected candidate will be responsible for managing regulatory and artwork activities associated with





new Marketing Authorizations (MAs)

and lifecycle management of products registered via

MRP, DCP, and CP procedures .

Key tasks include:

Supporting dossier preparation and submission activities
Managing

Product Operating Licenses (POL)

assignment
Coordinating

artwork creation, review, and approval

(carton boxes, labeling, and PILs)
Maintaining and updating national regulatory databases
Submitting applications via

AIFA Front End / CESP

platforms
Handling

End of Procedure (EoP)

communications with AIFA
Managing national implementation of variations under the

“Silenzio/Assenso”

procedure
Overseeing publication of regulatory updates in the

Italian Official Gazette
Managing

Farmastampati

processes
Ensuring accurate maintenance of the

XEVMPD database

Education

Degree in Life Sciences or a related field (preferred)

Professional Experience

1–2 years of experience in a Regulatory Affairs department within the pharmaceutical industry xlwpduy
Practical experience in

artwork preparation and review

for packaging materials (cartons, labels, PILs)

Language Skills

Native or fluent

Italian
Good command of

English

Technical Skills

Strong knowledge of

QRD templates

and

Blue Box requirements
Proficiency in Microsoft Office (Excel, Word, PowerPoint) and PDF tools
Familiarity with

AIFA Front End

and submission systems
Experience with virtual collaboration tools (e.g. Microsoft Teams, GoToMeeting)

Core Competencies

Strong attention to detail and accuracy
Excellent organizational and planning skills
Effective communication and interpersonal abilities
Results-oriented with a proactive mindset
High level of integrity and strong work ethic

Location

Milan, Italy

(Italian Affiliate of Sun Pharma)
Hybrid working model:

2 days in the office

📌 Regulatory Affairs Artwork Specialist (Torino)
🏢 SUN PHARMA
📍 Torino