Tim Joiner, Quality & Auditing Expert, has joined Qserve Group US as a U.S. Associate, where he is part of the Medical Devices team and is based in the US.
His background lies in the medical device and pharmaceutical industries for over 20 years, where he has been working on designing, implementing, and improving multiple Quality Management Systems for medical device organizations to meet domestic and international regulations, and product design assessments and reviews. Tim holds a degree in Microbiology and certifications in Lean Six Sigma Yellow Belt and Certified Quality Auditor.
There’s a
personal profile available on this website where Tim explains more about his experience and his core competencies.
About Qserve GroupQserve’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 to support manufacturers or distributors of medical devices and in vitro diagnostics. Check our
current vacancies.