Regulatory & Quality Affairs Specialist (Medical Devices)

Regulatory & Quality Affairs Specialist (Medical Devices Development)

DeepTech medical devices company with high growth potential is seeking to incorporate:

A young researcher who wants to direct their professional development in the areas of quality and regulatory affairs in the final phase of medical device development, for market launch in the short-medium term.

Join a highly innovative company, a spin-off of a leading technology center in the medical devices area. The company collaborates with several R&D and development teams from leading institutions.

Functions:

Participate fully in the development of the quality and regulatory areas of the medical devices that the company is developing for market launch. This implies continuous collaboration with the company's R&D teams due to the involvement of regulatory and quality assurance aspects in the advanced phases of research and development of the devices.

Also, participate in the development/coordination of necessary clinical studies.

Opportunity for a professional career with growth expectations in line with the company's growth.

Develop in a dynamic and agile team to adapt to needs, which becomes an opportunity to collaborate and gain experience in various company departments, in addition to the main functions of the position.

Essential Characteristics:

• Young Doctor with a degree homogeneous in Spain.
• Ph.D. in areas of science, health, or engineering.
• Knowledge of quality systems in health areas.
• Degree in pharmacy, chemistry, biotechnology, human biology, bioengineering, biomedical engineering, engineering, and related degrees.
• Master's in Regulatory or Quality Affairs or related fields.
• Specific knowledge of quality systems and/or regulatory affairs applied to medical device or pharmaceutical development companies.
• Knowledge of tests applied to medical devices (physical, engineering, biological, medical, ...)
• Dynamic person with high capacity for action.
• Flexible person with continuous adaptation capacity to the needs that arise in innovative young companies.

Contract Type:

• Fixed, full-time
• Flexible schedule
• Hybrid format (on-site and remote)

Please send your CV and cover letter, specifically indicating your knowledge and experience in the areas of quality and regulatory affairs.