Qserve Group is pleased to announce that Esther Sánchez and Maria Camara Torres have joined our team to further expand its capabilities in supporting the clinical and medical device industries worldwide.
Esther has joined Qserve as a consultant where she will be working as a medical writer. She is a biomedical engineer from Mexico and has held several positions in the medical device industry and worked as a biomedical engineer in hospitals. She gained experience with a broad range of medical devices in cardiology, suture, and orthopedic implants until she decided to pursue her career abroad. Esther is finishing her PhD about the primary stability of cementless knee implants, where she designed and performed experimental tests and computer simulations on different types of knee implants. She is
now involved in planning and preparing Clinical Evaluations, varying from writing Clinical Evaluation plans and reports and performing Literature searches to preparing Post-Market Clinical Follow-up strategies and plans.
Over the past 6 years Maria has worked as a researcher in the Tissue Engineering and Regenerative Medicine field, where she acquired a broad interdisciplinary experience in material science, cell biology and biofabrication. In particular, she worked on projects aiming at developing injectable anisotropic hydrogels for tissue engineering applications, as well as 3D printed biodegradable implantable scaffolds for bone regeneration. Maria has joined Qserve as a medical writer in Clinical Affairs and uses her knowledge of Clinical regulatory requirements and works together with different disciplines across organizations with the aim to provide a suitable clinical evaluation that suits the profile of the manufacturer.
About Qserve Group
Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We serve to guide manufacturers in gaining and maintaining compliance as well as conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years’ worth of combined expertise in the medical field. Having teams in the EU, USA, and China provides a global footprint for global regulatory, clinical, CRO and quality services.
Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs or auditing in medical devices. Check our current vacancies.