Quality management consultant

Quality management consultant

Life science jobs

Information

Are you comfortable in a management QA role just as much as you would like to perform more operational QA tasks? What are your responsibilities? - You preserve and improve quality management systems: - You provide advice, support and approval during root cause investigation, corrective/preventive actions (CAPA) and change control of procedures and processes. - You are in charge of timely review and approval of protocols, reports and deviations - You ensure that quality policies, procedures and programs are properly implemented in daily GxP operations and remain up to date. - You monitor compliance and ensure validated status of GMP processes and systems. Who are we looking for? - You have a master's degree - You have a first experience in GMP and you are familiar with manufacturing processes and operations, GxP guidelines, ISO regulations,… - Knowlegde of Quality Management Systems (CAPA, deviations, audits,…) What's in it for you? - QbD is a healthy company with a strong growth and international ambitions. In addition to a very attractive salary package, we can offer you the following advantages: - A company with a clear strategy and ambition - We've got your back! Our HR Business Partners follow you closely, giving you the opportunity to shape your career. - Thanks to our flat organization, we have short communication lines and you can always come to us. - Standing still means going backwards. With our extensive training package and our periodic knowledge-sharing moments, we offer you many opportunities to continuously learn, to expand or specialize your knowledge and skills and to gain new expertise. - Get to know your colleagues outside the work environment! Teambuilding and fun activities are planned on a monthly basis. A comedy night or quiz night? Interested? Send your CV and motivation letter to jobs@qbd.eu. Want some more info? https://jobs.qbd.eu/en/vacancies/vacancy-quality-management-consultant/
Quality by DesignQbD is a partner in the development of qualitative and advances therapies and technologies for the benefit of patients and consumers worldwide. Our knowledge and expertise are at our clients’ disposal. We gained this expertise in following main domains: Quality Assurance Validation & Qualification Regulatory Affairs Projectmanagement & Support Within our two focal points (ATMPs and Medical Devices), we want to take on a pioneering role on a global level and help determine the rules in these two fields. In the short and mid long term, we aim to be present in 5 European countries by starting up QbD subsidiaries or via acquisitions. Additional to those, we also aim to have a few subsidiaries in North-America and Asia. It’s QbD’s ambition to: Being present in all continents worldwide Being present in minimum 5 European countries with more than 50 staff members per country Having an active participation in at least one company dealing with ATMPs and one company dealing with medical devices Being a full service knowledge organization with full expertise in:Process development within ATMPs Quality Assurance and Regulatory Medical Devices Artificial Intelligence/Deep Learning Become, with QbD Software, a premium supplier for the life sciences Having CSV outsourcing/off shoring/near shoring on point

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