Technology Transfer Engineer

Technology Transfer Engineer

Consultancy

Information

Do you want to be involved in the progress from drug or medical device discovery over product development and clinical trials to full-scale commercialization? Are you triggered by new product introduction and do you easily master new innovative techniques? Then apply now as a technical transfer lead! Your responsibilities: Involved in different transfer projects, e.g.: * Transfer new technologies to manufacturing by developing and validate the production processes * Support our clients in bringing new products or drugs to the market * Assist spin-offs with the scale-up to manufacturing and process improvement * Take up project lead roles during outsourcing or relocations of products * Monitor and manage new product introduction and industrialization projects * Manage project teams and establish efficient industrialization procedures * Ensure compliance with national and international (EU, FDA) regulatory requirements and other applicable guidelines What do we offer? The QbD group is a healthy and international company with strong growth ambitions (organic and inorganic). In addition to a competitive salary package (company car, fuel card, insurances, meal vouchers, ...), we can offer you: * a clear strategy and ambition - our QbDream! * short communication lines, easy decision making & impact - you are heard! * value and data driven company * sustainable relationships - human centric approach * being part of an award winning company More info? https://qbdgroup.com/en/vacancies/technology-transfer-engineer/
QbD Groupbooth 86-87-94-95The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. We are a multinational company with over 480 high-qualified employees and are growing fast as we realise our ambitions of expanding worldwide. 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. • Lab Services: 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 & services: 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). • Business & Communications: We help you launch your product to market by providing marketing and communication services, business development support, and sales strategy.

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