Regulatory Affairs Associate – Collaborative Team

Location:

North Holland – Noord-Holland, Nederland, Netherlands

Salary:

€45000 – €60000 per annum

Type:

Permanent

Main Industry:

Search Health, Nursing & Social Services Jobs

Advertiser:

NonStop Consulting

Job ID:

131080769

Posted On: 

12 September 2024

A market leader in generics with a robust and innovative Branded department dedicated to the development of novel products is looking for a Reglatory Affairs Associate. This dynamic environment not only allows you to leverage your scientific background but also offers a unique opportunity to be part of a smaller, growing team where communication is swift and collaborative. With exciting new products in the pipeline and a commitment to operational excellence, this organization is not just about moving products to market; it is about shaping the future of pharmaceuticals.

Benefits:

– Enjoy the flexibility of three days of remote work, enhancing your work-life balance and allowing you to invest time in personal interests and family.

– Contribute to a broad array of Regulatory Affairs activities, from pre-approval to post-approval, that encourages skill diversification and professional development.

– Be part of a culture that actively drives innovation and adapts quickly to market changes, ensuring your role remains engaging and impactful.

Responsibilities:

– Manage all aspects of regulatory activities, ensuring that new products flow smoothly from development to market launch, showcasing a direct impact on the organization’s success.

– Collaborate closely with your team and global partners on submissions, registrations, and lifecycle management, enhancing your operational expertise within an international context.

– Take responsibility for labelling and submissions, gaining valuable exposure that will further your career while contributing to the advancement of innovative products.

Requirements:

– Hold a scientific degree that empowers you to contribute meaningfully to the regulatory processes.

– Bring 2-3 years of experience in Regulatory Affairs within the pharmaceutical industry, ideally with exposure to both small molecules and biologics.

– Competence to navigate the complexities of pre-approval activities, labelling, and registrations, utilizing your skills to play a critical role in the successful market introduction of new products.

If interested, apply now. Don’t miss out on what could be a great opportunity for you!

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