Lead Commissioning & Qualification SME

Lead Commissioning & Qualification SME

Consultancy

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From introducing new products to the market to launching new technologies and processes, our project managers make sure everything runs smoothly. As a Lead Commissioning & Qualification SME in QbD’s Project Management Organization (PMO) you support companies with the deliverables they have requested in the form of a project. This includes managing timelines, resources, and budgets, regularly updating the client on progress, and discussing any risks that may affect the project. You love to take care of: * managing various projects within highly innovative environments * performing quick scans or gap analysis, incl debrief to the stakeholders * drafting, implementing and managing project plans (timeline, budget, resources) * chairing steering committees * managing and coaching project consultants/team members with a multidisciplinary background In short, we rely on you for the successful follow-up and implementation of our most important projects that will further draft the future of tomorrow’s healthcare. 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, 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 https://qbdgroup.com/en/vacancies/lead-commissioning-qualification-sme/
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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