Global Regulatory Affairs IVD Specialist / Global Regulatory Affairs IVD Specialistess

Job Opportunity: Regulatory Affairs Specialist

Proclinical is seeking a Regulatory Affairs Specialist to join a dynamic team within the diagnostics industry. This global role offers the opportunity to work on innovative products in areas such as oncology and diabetes diagnostics. You will play a key role in regulatory processes and contribute to cross-functional projects, gaining valuable experience in a collaborative environment.

Key Responsibilities

• Creation and adaptation of global regulatory documents.
• Maintain regular communication with regulatory authorities.
• Represent regulatory strategies in cross-departmental meetings during product development projects.

Key Skills and Requirements

• Experience in regulatory affairs within the in-vitro diagnostics (IVD) sector.
• Proficiency in German, both written and spoken.

Proclinical is a specialized recruitment consultancy offering career opportunities in the pharmaceutical, biopharmaceutical, biotechnology, and medical device industries. Proclinical Staffing is also an equal opportunity employer.

Apply online using the form below. Please note that only applications matching the job profile will be considered.