Regulatory Affairs Associate – Collaborative Global Team Role

Location:

East of Amsterdam – Noord-Holland, Nederland, Netherlands

Salary:

Negotiable

Type:

Permanent

Main Industry:

Search Health, Nursing & Social Services Jobs

Other Industries & Skills: 

Healthcare

Advertiser:

NonStop Consulting

Job ID:

132098680

Posted On: 

18 July 2025

Regulatory Affairs Associate – Collaborative Global Team Role

Are you ready to take your Regulatory Affairs career to the next level in a international environment?

Join our client, a global leader in consumer health innovation, and seize the opportunity to grow within a dynamic international operations team. Based just east of Amsterdam, this organization is known for pushing the boundaries of healthcare and upholding the highest product safety standards.

You will work closely with diverse, cross-functional teams across multiple markets, gaining valuable exposure to various regulatory landscapes. Through collaboration with senior leadership, you will sharpen your skills in regulatory submissions, dossier management, and compliance oversight throughout the product lifecycle.

Benefits:

* Work in a dynamic global environment with diverse cross-functional collaboration, boosting your skills and professional network.
* Play a key role in ensuring product quality and patient safety, making a real impact on healthcare innovation.
* Develop project management skills through direct interaction with senior pharmaceutical industry leaders.

Role Responsibilities:

* Collaborate with cross-functional teams to ensure regulatory compliance and align product strategies with global standards, driving the company’s mission of continuous improvement in healthcare.
* Directly contribute to ensuring the quality and safety of products, impacting patient safety and innovation in healthcare.
* Manage regulatory processes and strategies, working closely with senior management and key stakeholders to maintain the organization’s standards of excellence.

Requirements:

* Hold a Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related field, offering opportunities to leverage your academic background.
* Minimum of 2 years experience in regulatory affairs within the pharmaceutical or healthcare industry.
* Good familiarity with EMA/ICH guidelines and practical exposure to eCTD submissions, including CMC Module 3.
* Fluent in both Dutch and English (spoken and written) is required.

If you’re ready to advance your career with a company dedicated to innovation and professional development, apply now to become an Regulatory Affairs Associate.

If this job appeals to you please apply here or send your CV to me, Arianna Coia, on the NonStop Consulting website or on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.

Do you have any disability or condition that could affect you in the application and interview process? Please feel free to share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We assure you this information will not have any negative effect on the interview process outcome.

About NonStop: We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We’re passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting (nonstopconsulting), for more information, to browse all our roles, or to let us know how we can help you.

To help us track our recruitment effort, please indicate in your email/cover letter where (vacanciesin.eu) you saw this job posting.