Vai al contenuto principale

Junior R&D – Medical Devices Consultant

 

We are a service provider companyleader in the Pharmaceutical and Medical Device sectors since 1998, with more than 1500 employees45+ nationalities and 30 subsidiaries all over the world (Europe, Asia and the Americas). Joining PQE Group means being a part of a multicultural and challenging company, with many local and international projects and colleagues from all over the world.

Due to a constant growth, PQE Group is looking for a Junior R&D – Medical Devices Consultant who will support our clients based in MirandolaItaly.

Joining PQE will give you the opportunity to acquire the following professional competencies:

  • Drafting of the design documentation: design requirements, design plans, design inputs-outputs traceability matrix, verification and validation protocols and reports, design review reports, DHF;

  • Participation in design change activities and management of design change documentation;

  • Participation in planning and conducting design verification and validation activities;

  • Participation in planning and conducting test method validation activities;

  • Participation in design transfer activities;

  • Manage (i.e. promote, coordinate and document) the Risk Management activities during the Product Development Process, in relation to product modifications and during post-marketing surveillance;

  • Prepare and maintain Summary Technical Documentation (STED) for regulatory purposes;

  • Cooperate with internal departments during the Product Development Process to permit regulatory release (CE Mark, FDA approval etc.);

  • Prepare and maintain the Technical File documentation (e.g. Device Master File) for new products or modified products and cooperate with Regulatory Affairs Area to prepare regulatory submissions (e.g. 510K pre-market notifications);

  • Assists regulatory department with FDA, CE, and other regulatory submissions;

  • Assists in implementing and maintaining a quality system that is compliant with ISO 13485 and with quality system regulation requirements.

Requirements:

  • Technical Degree in Biomedical Engineering

  • Full availability to Travel up to 75%

  • English language fluency in speaking and writing (at least B2/C1)

  • Availability for body rental activities (from 1 to 3 years of on-site permanence by our clients’ sites)

Location: Mirandola, Italy

Our collaborators are engaged, developed, challenged and well-rewarded for performance. We recognize the importance of leadership at all levels of our organization in order to succeed in a challenging business environment, and we are committed to providing practical processes and programs to identify, develop and inspire all our current and future leaders.

 

 

Degrees of interest: Technical Degree in Biomedical Engineering

To apply to this opportunity, just click on APPLY. After clicking, you can add a motivation letter. It's recommended but not compulsory.

Important: if the job description is in english, than also the motivation letter and the cv saved into the platform must be in english.


Apply