University degree in Chemistry, Pharmacy or other life science degree Significant experience in Quality Management for Pharmaceutical and Medical Device products Excellent knowledge on GMP guidelines, ideally from production Significant leadership experience Travelling around 10-20% Fluency in German &
Quality Management - Responsible for Risk Management REQUIREMENTS - Strong experience in the field of Medical Devices, both in Quality and Operations - Strong knowledge of ISO 13485 and FDA 21CFR 820 - Knowledge of GMP preferred - Experience within the Automotive, Aerospace
this role you will be responsible for managing 10+ manufacturing sites in Europe from a quality perspective. RESPONSIBILITIES - Making sure that Plants are in compliance according to relevant guidelines such as cGMP - Representing European plants on Quality matters - End
will be responsible for managing 10+ manufacturing sites in Europe from a quality perspective. RESPONSIBILITIES - Making sure that Plants are in compliance according to relevant guidelines such as cGMP - Representing European plants on Quality matters - End responsible
and the EU In Vitro Diagnostics Directive (98/79/EC) - Further develop and implement the quality management system culture within the company - Ensure that all customer complaints are responded to within appropriate time frames and escalated appropriately through the vigilance process when required
The Quality Assurance director will be responsible for leading the QA department (both in Belgium and on a global level) in order to maintain and promote quality and compliance throughout the company. RESPONSIBILITIES - Provide leadership to the team - Responsible for
Quality Engineer with German Września NR REF.: 1079679 Dla naszego Klienta, zagranicznego zakładu produkcyjnego z branży automotive poszukujemy kandydatów na stanowiskoInżynier Jakości z językiem niemieckimOsoba zatrudniona na tym stanowisku będzie odpowiedzialna za wspieranie
department's QA Officers (14 FTE) - Update the QMS database - Participate in multidisciplinary meetings - Lead CAPA activities and CAPA reviews - Preparation of internal audits REQUIREMENTS - At least 10 years of experience in Quality Assurance in the medical devices industry ...
internationally. RESPONSIBILITIES - Set up the Quality Strategies - Lead the implementation of Coninuous improvements tools and QMS - Contact person for Health Authorities - Establish Quality Agreements with subcontractors, supliers and packaging organizations - Head responsible for
SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...
ensuring dispensed to the general network service, as well as suppliers and customers with the aim of providing quality service in time • Corporate with Technical support group in the area of technical support, training and support, ensuring product quality and training, product surveys and reports
Person in this position will be coordinating all the activities with the HQ located abroad and will actively participate in Steering Committee. Industrial Director will report to President of the Board, located abroad.To be suitable for this role you should posses Higher Technical Education and minimum
VEO Worldwide Services is an international group of companies that provides B2B solutions to its partners. Over 500 specialists support them in field of acquisition, sales, logistics, quality and management, IT, finances and HR. As a thriving company we constantly invest in the quality of our
in Food, Bio-tech or Chemicals - 10+ years of experience in the industry - Fluent in English, knowledge of Dutch, German, Italian or French is beneficial - Project/Program management experience - Strong influencer, motivator and communicator - Entrepreneurial and innovative mindset - Resultant ...
REQUIREMENTS - Master or PhD in Food, Bio-tech or Chemicals - 10+ years of experience in the industry - Fluent in English, knowledge of Dutch, German, Italian or French is beneficial - Project/Program management experience - Strong influencer, motivator and communicator - Entrepreneurial and
Quality Assurance Manager, you will lead complaints evaluations, act as the first point of contact for internal and external auditing of the Quality Management System. The challenge in this role is to own all the processes and to find creative ways to meet the requirements with a hands-on approach in an
guidance for the various elements of the Quality System, for example, to ensure process control, consistent supplier qualification practices and identifies/recommends opportunities for continuous improvement (internal/external). Moderate level of application of the appropriate statistical tools to analyze
complaints - Actively provide support to R&D department REQUIREMENTS - Thorough knowledge of ISO 13485 - 5 years of experience within a quality department in a Medical Device environment - Knowledge of clean room production requirements - Diplomatic handling of customers and