Internship Regulatory Affairs at Reckitt
20141 Milano, Lombardia, Italy -
Full Time


Start Date

Immediate

Expiry Date

22 May, 25

Salary

0.0

Posted On

23 Feb, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Product Lifecycle Management, English, Collaboration, Commercial Awareness

Industry

Pharmaceuticals

Description

Home to the world’s best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.
Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.

THE EXPERIENCE WE’RE LOOKING FOR

  • Master degree in Pharmacy/Pharmaceutical Chemistry/Biotechnology
  • Good level of English
  • Good knowledge of Microsoft Office/Power Point

THE SKILLS FOR SUCCESS

R&D, Product Lifecycle Management, Commercial Awareness, Business Partnership, Collaboration, Propose improvement, Accountability, Adaptability, Formulation, Science, Chemistry.

EQUALITY

We recognise that in real life, great people don’t always ‘tick all the boxes’. That’s why we hire for potential as well as experience. Even if you don’t meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.
All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law

Responsibilities

ABOUT THE ROLE

You’ll be part of a team where outperformance and achievement are the common ground to build growth.
Complying with Global standards and local procedures, you’ll help providing safe, effective and compliant products to customers, consumers and patients, as well as accurate, consistent and effective information to internal and external stakeholders.

YOUR RESPONSIBILITIES

  • Support in the lifecycle management of medicines (variations, renewal, etc.), medical devices and food supplement under OTC portfolio and preparation of documents to be submitted to Authorities
  • Support the team in revising and approving Artworks
  • Support the process of medical information and advertising ensuring that promotional and educational materials are consistent with scientific ratio and meet applicable regulatory requirements
  • Support the team to prepare and submit the relevant documentation related to HCP materials and consumers advertising for the whole health brands
  • Ensure compliance with applicable local and global laws, regulations, guidelines and Company policies
  • Maintaining of local medical database and systems
  • Monitoring of AIFA/Regulatory websites in order to detect law changes
  • Provide regulatory support and cooperate with marketing to ensure alignment on activities and on time delivery
  • Support in managing request from other departments and global regulatory
  • Support in the preparation of presentations for internal/external projects
  • Support the management of parallel import requests
Loading...