Register Your Interest - Associate Specialist, Regional Regulatory Operations Placement 2027 (EU + EEMEA)

Associate Specialist, Regional Regulatory Operations Placement 2027 (EU + EEMEA)

This role will be based in our modern state-of-the-art co-working facilities in Moorgate, London. This site, at the heart of London provides fantastic amenities, support services and collaborative workspaces with convenient transport links.

Brief Description of Position

You will work within our Global Regulatory Affairs and Clinical Safety (GRACS) organisation, in the Regulatory Affairs Operations International team, which is based in Europe.

You will support the regulatory submission creation and the registration tracking of the company regulatory submission targets from a regulatory operational perspective across the Europe, Middle East, and Africa regions (EU & EEMEA).

As a member of cross-functional team and for the assigned products, you will support the team to manage all operational aspects for submission planning and execution of Original Marketing Application (OMA) and post-approval regulatory changes.

This position requires a keen interest of the regulatory landscape, its registration procedures and a willingness to understand the technical requirements for dossiers.

Primary Activities include but are not limited to:

• Support the planning and managing of regulatory operation projects from authorisation through delivery to country regulatory affairs teams and/or Health Authorities.
• Supporting the regulatory submission plan for the assigned projects/products and maintaining the related project milestones.
• Participate in cross-functional forums and meetings
• With manager support, drive the submission assembly and delivery process with the Global and/or Regional Submission Publishing team to ensure timely assembly, publishing and archival of assigned products/submissions as per the agreed timelines.
• Responsible for accessing and maintaining the regulatory systems and databases to fulfill daily functions.
• Assist in identifying opportunities to continually improve the efficiency of the submission processes and systems and participate in small-scale process improvement projects.
• Learn knowledge on the regional regulatory procedures on internal and external guidelines and standards.

Qualifications, Skills & Experience

Requirements

• You must be currently studying at a UK university and will be looking to complete a 12-month student internship as part of your undergraduate degree.
• Technical Requirements are flexible, but an affinity for and capability to learn Regulatory Information Management systems to execute operational tasks will be a significant asset.

Equal Opportunity Employer:

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Deadline: Ongoing

Job Type:

Placement (10 Months+)

Job Roles:

Pharmaceutical

Logistics and Operations

Computer Science

Business Operations

Locations:

London

About MSD

At MSD, we are inspired by a shared vision and mission to save and improve lives. For 130 years, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases in pursuit of our mission to save and improve lives.

This score is based on honest feedback written by students who’ve worked at MSD.

#J-18808-Ljbffr

Full job description from WhatJobs. Apply for this role →