Admin Move-graduate - London, United Kingdom - MSD

MSD

Verified Company

London, United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Job overview:

Our Regulatory Affairs teams bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies.

We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.

24 Month Graduate scheme encompassing two 12 month rotations in International Regulatory CMC (Chemistry, Manufacturing & Control), and Regulatory Affairs Europe, both based at our Moorgate, London office.

You will spend ?

12 months in International Regulatory International CMC

International Regulatory Affairs CMC is a key component of our company's strategy to build regional Chemistry Manufacturing and Controls regulatory knowledge and effective local relationships with country offices to deliver appropriate regulatory strategies and deliver right first-time regulatory submissions.

As part of the EMEA team you will be one of the regional experts for CMC in Europe, Middle East and Africa.

Duties & responsibilities

Assess changes to dossiers in the EMEA region and review submission packages
Liaise with colleagues across the region and globally
Work alongside our team in health authority interactions and engagements
Work alongside our team to deliver on operational excellence projects and best practises for regulatory science

And

12 months in Regulatory Affairs Europe - RAE**The RAE team brings new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. It is part of Global the Regulatory Affairs and Clinical Safety organization and covers a wide range of activities related to getting products and keeping them on the market. Our large portfolio in Vaccines, Infectious Diseases and General Medicine includes medicinal products at all stages of the regulatory life-cycle and span a number of therapeutic areas. It provides the chance to learn something new every day.

Duties & responsibilities

Support the development and submission of regulatory review submissions for new and already authorised medicines in Europe, Switzerland and Great Britain
Liaise with colleagues across the European region and across the enterprise
Work alongside our team in health authority interactions and engagements
Work alongside our team to deliver on operational excellence projects and best practises for regulatory science

Eligibility/Education

You will be looking to complete BSc in a scientific discipline such as chemistry, biological sciences, engineering, or a related field in 2024 or within the last two years.
Fields of study include (but are not limited to) Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry (or equivalent qualification)

Requirement:
skill. Competencies and behaviours

Operates with a high level of integrity, transparency and accountability
Comprehends and aligns with our organization's core values
Aligns and fosters a culture of diversity and inclusivity
Demonstrates initiative, proactivity and academic curiosity
Encourages and boosts their colleagues through teamwork
Demonstrates clear and effective communication
Demonstrates a desire to learn and improve their performance through feedback
Ability to work both independently and collaboratively in a team structure

Search Firm Representatives Please Read Carefully

Employee Status:

Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

Valid Driving License:

Hazardous Material(s):

Requisition ID:
R259281