(Sr.) Regulatory Specialist

F. Hoffmann-La Roche Gruppe; Valencia; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

Join a leading company in the healthcare sector dedicated to driving innovation and ensuring access to healthcare solutions. The role focuses on medical regulatory affairs, requiring a strong background in regulatory compliance, along with excellent communication and organizational skills. This position contributes to fulfilling product registration goals while nurturing key relationships within the company.

Formación

• At least 5 years of experience in medical regulatory affairs.

Responsabilidades

• Work with sales and marketing to fulfill product registration plans.
• Provide regulatory support to the Regulatory Department.
• Maintain clear records and organized documentation.

Conocimientos

Proficient in spoken and written English

Skilled in MS Office applications

Understanding medical device regulations

Educación

Bachelor’s degree or above in medical, bioengineering, clinical medicine, or biochemistry

Descripción del empleo

At Roche, you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted, and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop, and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.

• Working with sales and marketing departments to fulfill product registration plans for specific product lines. Achieve R&D expectations on product registration.
• Establishing and maintaining good relationships with key contacts. Providing valuable suggestions to the company.
• Supporting Regulatory Department by providing active and strong regulatory support as needed.
• Handling daily tasks proactively. Keeping records, maintaining clear filing, and organizing all documents.
• Taking on other projects or tasks assigned by the line manager.
• Understanding and fulfilling responsibilities related to line manager's SHE tasks and duties as defined in the SHE handbook.

Who you are

• Holding a bachelor’s degree or above in medical, bioengineering, clinical medicine, or biochemistry.
• Having at least 5 years of experience in medical regulatory affairs.
• Proficient in both spoken and written English and skilled in MS Office applications.
• Understanding medical device regulations .

Who we are

Driven by a vision for a healthier future, more than 100,000 employees worldwide are dedicated to advancing science and ensuring access to healthcare today and for generations to come. Our efforts have resulted in over 26 million people treated with our medicines and more than 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and aim high to deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

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