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 &
the internal & external audits - The company has serveral laboratories both in and outside of Europe - In general: set up a quality plan REQUIREMENTS - PhD or MSc with a relevant background - Atleast 5 years of hands-on Quality Assurance experience (focus on GCP, GLP
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
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
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
The Quality Operations Director provide strategic leadership to the Quality Business Unit. This includes the implementation of Continuous improvement tools and programs in order to enhance the Quality level of the Quality department. Besides, you will need to manage a team of 9 Quality memeber located
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 ...
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
to provide continual rise through creating professional relationships with clients. COMMERCIAL DIRECTOR Expectations: at least 5 years of professional experience in coordinating commercial teams, preferably in a multinational company; very good managerial, communication, organizational and negotiation
training in teams and react to this - QMS maintenance - Report to the Director Quality Global REQUIREMENTS - Profound knowledge of ISO 13485 and ISO 9001 - Knowledge of IEC 60601 - Experience with FDA 21 CFR 820 - Able to interact with all different departments within
up of a quality system according to ISO 13485 requirements - Responsible for overseeing the whole R&D Department (resource, expertise and budget planning, definition and improvement of processes, definition of product development and technology strategy) - Overseeing three direct reports (two R&D
Continuous Improvement Director. You will provide analytical expertise to the businesses in support of the organizations’ improvement programme, focusing on business performance. Your focus will be to Design Lean Strategies for Continuous Improvement for the BU across the Value Chain. You will provide
initiatives. • Facilitate Accelerate workouts, value stream mapping sessions and activities to achieve project objectives. • Quality Specific Goals: Aware of and comply with the Quality Policy, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they
you will be working closely together with suppliers of plastics and resins to make sure the products meet the company's quality and food safety standards. A team of QA specialists will be build the coming next months and you will have 2 or 3 direct reports. You report directly to the management team ...
management - Managing and the Quality and Food Safety team - Apprise and evolve potential new suppliers - Project management, continuous improvement - Supplier auditing - Systems: ISO 9001, GMP, BRC/IFS, FSSC 22000 REQUIREMENTS - Bachelor Chemie, Food Science Wageningen or
to development quality system - Identify training gaps and areas for improving - Support regulatory compliance to GCP/GVP REQUIREMENTS - University degree in Life Sciences or related field - At least 5 yeas of experience in highly regulated pharma environment - Experience dealing
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 ...