Arbetsbeskrivning

Job description

Do you have experience in Regulatory Affairs and thrive in a global team setting? Are you seeking an exciting new challenge in the dynamic world of Regulatory affairs)? If so, this is the role for you!

We at Randstad Life Science are continuously looking for qualified regulatory affairs professionals for future assignments. As a consultant with us, you become part of a dynamic network where your knowledge and experience can be used in various projects within quality management. Therefore, we encourage candidates with a relevant background and expertise in regulatory affairs, from the pharmaceutical or medtech industry, to reach out even if we currently don’t have a listed position.

Why submit a spontaneous application to us?

At Randstad Life Science, we are always interested in getting to know competent and driven individuals interested in working as consultants within the pharmaceutical and medtech industry. Even if we are not currently advertising a specific Reg role, we highly value proactive applications and look forward to exploring future collaboration opportunities with the right candidates.

If this has piqued your interest - we welcome your application! Please make sure your CV and personal letter are in the same document. We will reach out to you if a position that fits your qualifications becomes available.

Responsibilities

Key Responsibilities:

• Collaborate with teams to ensure efficient and seamless Regulatory Information Management across all stages.
• Oversee the regulatory data for assigned areas, ensuring alignment with industry standards, regulatory requirements, and business processes.
• Prepare and submit regulatory data submissions (XEVMPD, IDMP, etc.) to health authorities.
• Continuously develop expertise in areas vital to successful RIM execution, with a focus on technical skills and international regulations.
• Engage with partners, affiliates, and stakeholders to manage regulatory data and ensure adherence to standards and procedures.
• Monitor legislative changes impacting regulatory information, reviewing and assessing regulations, guidelines, and technical specifications.
• Act as a subject matter expert in the analysis, management, and quality control of regulatory data standards.

If you're excited about this type of position in the future! Submit your application and apply now!

Qualifications

What We’re Looking For:

Required:

• University degree in life sciences or equivalent experience in the pharmaceutical/medical industry.
• Strong understanding of the pharmaceutical drug development process.
• Excellent analytical and critical thinking abilities.

Preferred:

• Strong problem-solving and conflict resolution skills.
• Ability to prioritize, set performance targets, and manage projects effectively.
• Ability to innovate and implement best practices through business process analysis and design.

Collaboration and continuous learning are core to how we operate and succeed. In Regulatory, we work together across global teams, therapeutic areas, and the external community to share insights and expertise. We are proactive, self-driven individuals who take ownership of our growth, both personally and professionally.

We are a compassionate, results-driven team, always ready to take initiative. If this resonates with you, we invite you 

to apply for the Reg role.

About the company

Randstad

At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward.