QbD Group
Jose DeColsa has a diverse range of work experience. Jose started their career as an Assistant Export Manager at Alimentaria del Duero in 2006 and then moved on to become the Deputy Manager Service Delivery at HP in 2008. In 2014, they joined Capsugel as a Finance Controller, where they provided innovative dosage forms and solutions to healthcare companies. From 2016 to 2018, Jose worked as an International Development Manager & Business Controller at Quality by Design, helping companies in the pharmaceutical, biotechnological, cosmetics, and healthcare industries manage quality control systems. Jose then became the International Business Director at Quality by Design in 2018, focusing on the life sciences industry. Lastly, in 2019, Jose became the Managing Director for Spain at QBD Group, where they gained the trust of employees and clients and provided services in validation, quality assurance, regulatory affairs, and more in the pharmaceutical, biotechnology, healthcare, medical devices, and cosmetics fields.
Jose DeColsa attended the Universidad de Salamanca, but no specific information regarding the start year, end year, degree name, or field of study is available.
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QbD Group
The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. We are a multinational company with over 450 high-qualified employees. Our experienced team serves the wider life science industry, with a strong focus on ATMPs, medical devices, IVDs, and digital health, thanks to the specific expertise we have built in these areas. The services we offer fall under the following divisions: • Regulatory Affairs: We help our clients in their journey throughout the entire drug and medical device regulatory lifecycle. • Clinical: We are an expert clinical solutions provider specialized in medical devices and biotech, offering global CRO services and consultancy. • Qualification and Validation: We guarantee that products meet quality demands and comply with regulation through the qualification and validation of your processes, equipment, and software. • Quality Assurance: We offer the full range of QA services necessary to get your product to market in a safe and compliant way, including auditing from certified auditors, setting up your QMS, and all QP (Qualified Person) activities. • Quality Control: Our QC division consists of a GMP laboratory that offers analytical services for testing pharmaceutical raw materials, excipients, and release testing of finished products. • Software solutions: Cloud-based and pre-validated Quality Management Software built for the life sciences, as well as eIFU services which enable IVD and MD manufacturers to digitalize paper Instructions For Use (IFU). • Go to market: We help you launch your product to market by providing marketing and communication services, business development support and sales strategy.