Joshua Spencer joins Qserve
Date d'envoi: septembre 06, 2021
Qserve Group is pleased to announce that Joshua Spencer has joined our team to further expand its capabilities in supporting the medical device and IVD industries worldwide.
Working for Qserve Group UK Ltd, Joshua works as consultant whose responsibilities range from the running of literature searches and reviews, as well as writing various reports and documents for a variety of regulatory activities. As consultant he supports the IVD team in various projects.
He is a qualified biochemist and microbiologist having graduated from the University of Nottingham Trent with a Bachelors (Honours) and received a diploma in professional practice (DIPP) for his placement year within a small biotech company. Joshua’s experiences at that biotech company provided him with experience in manufacturing according to ISO 13485 and working under IVD regulations. This included taking part with tasks centred around quality control (QC), taking responsibility for the maintenance of various laboratory equipment and its validation and helping ensure compliance under ISO 13485. With the completion of his degree, Joshua has been furthering his scope and understanding of the regulatory world applying his experiences in industry as part of the Qserve team. He will initially focus on the effective execution of literature searches for inclusion into a clients technical file as this is a new skill for the IVD regulatory world and very much in demand.
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
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