Associate Regulatory Affairs Director Join Innovative TeamNonStop Consulting

Zug , Zoug, Switzerland

Type: n/a

Category: Finance & Accounting

Requirements: English
Company: WhatJobs
Region: Zug , Zoug

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Associate Regulatory Affairs Director Join Innovative Team

Client:

NonStop Consulting

Location:

Zug

Job Category:

Consulting

Job Reference:

633c09c2e42f

Job Views:

4

Posted:

25.04.2025

Expiry Date:

09.06.2025

Job Description:

Join a Leading Regulatory Affairs Team!

About Our Client

With a diverse portfolio of iconic brands across 20 countries, our client operates in Australia & New Zealand, Asia, and Africa. Their team is dedicated to putting peoples health first every day, and they pride themselves on their unique blend of leadership and empowerment.

Our client, celebrated as a Best Place to Work in 2021, is a trailblazer in the health and wellness industry. Known for their innovation, motivation, and unwavering commitment to customer health, they offer a work environment that their employees love. Join the team to discover why!

The Opportunity

Our client is seeking an experienced Associate Regulatory Affairs Director, Europe, to become an integral part of their Regulatory Affairs team. This full-time role is pivotal in steering and managing strategic and operational regulatory activities across Europe, including the EEA, Eastern Europe, Switzerland, and the UK.

Key Responsibilities

• Oversee regulatory activities in Switzerland and coordinate those in the EEA, Eastern Europe, and the UK.
• Ensure compliance and support for the Middle Eastern and African markets where our client holds marketing authorizations.
• Implement and update regional Regulatory Affairs procedures and ensure staff training.
• Champion regulatory information management systems and ensure their alignment with organizational systems.
• Align regulatory affairs with business objectives, ensuring timely market introduction of new products.
• Interface with various key functional groups to provide quality regulatory input.
• Promote cross-regional regulatory collaboration and knowledge sharing.
• Develop and optimize regulatory strategies for new business opportunities in Europe.
• Conduct regulatory due diligence for new products and provide strategic regulatory guidance.
• Support major commercial expansion projects and the creation of product registration dossiers.

About You

To excel in this role, you should have a recognized degree in pharmacy, medicine, or a relevant science, and a minimum of 8-10 years of experience in the pharmaceutical industry, with at least 5 years in the European region.

Key Requirements

• Thorough understanding of regulatory requirements for a range of health-related products.
• Familiarity with clinical, regulatory, registration, and compliance principles.
• Strong project planning and organizational skills, with the ability to manage multiple projects.
• Excellent interpersonal, communication, and influencing skills.
• Ability to work independently and as part of a team.

Additional Requirements

• Occasional business travel.
• Commitment to the companys values.

Our client offers a supportive and dynamic work environment with a variety of benefits, including:

• Hybrid working arrangements.
• Health and wellness initiatives.
• Awards and recognition programs.
• A day off for your birthday!

Join a team where your expertise will make a significant impact on regulatory affairs across Europe and beyond! Apply today to be part of a company that values health, innovation, and excellence.

Contact me for more details:

For a confidential discussion about this role, or to apply, send your CV to (emailprotected) or call me, Angelina Andreenkova, Search Specialist Life Sciences Switzerland, at +41 445 08 23 19 (intern 3594).

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