REQUIREMENTS 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
will be responsible for all GCP/GVP actitivies. RESPONSIBILITIES - GCP/GVP auditing and inspections - Clinical Quality management - Contract management of service providers - Line Management of auditing team globally REQUIREMENTS - Strong
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
FDA 21CFR820 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
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 ...
the same time this position is far from easy. Our client is looking for a senior really talented Quality Manager. RESPONSIBILITIES - Bringing alignment and synergy through all 4 plants worldwide regarding quality for the total value stream. - Get the Quality up
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
implementation of training strategy for development quality. RESPONSIBILITIES - Line management responsibilities and leadership - Interdepartmental communication with internal and external stakeholders - Lead a quality team to implement and develop training programs related
Bachelor’s degree required. - Minimum 9 years of pharmaceutical clinical research and development experience - Minimum of 6 years of clinical quality assurance experience required - Experience working within a complex organization and demonstrated ability to work across functions and regions, at all levels
by developing, monitoring and continuously improving the suppliers' compliance and performance - Project and Change 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 ...
a very talented Director SHE EMEA who can support the plants in Europe in growing and development. + 10.000 SKU's (products), more than 8.000 employees in more than 28 countries, around 5 billion turnover. ROLE DESCRIPTION (Special high level role ...
a Sales Director Beverages. We are seeking for a highly motivated individual to manage its sales efforts in the Southern European region. You must be highly organized, entrepreneurial, and have a track record of growing territories. You are highly motivated and must be able to work well without
superiority. - Food safety: Ensure compliance of Co-Man on hygiene prerequisite and best practices, food safety index, control plans, surveillance plans. - Quality: Ensure the finished product quality is in line with our specifications and control the level of those specifications to keep quality consumer at
function of the pharmaceutical industry - Knowledge and experience in pharmaceutical operations, quality control, distribution and International regulations are essential - Knowledge of cGMPs, cGDPs regulations and requirements for pharmaceutical products distribution - Verbal, written and presentation
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
Meeting and exceeding requirements of both ISO and internal/external requirements is key. RESPONSIBILITIES - Development and implementation of Quality Tools, FMEA, SPC, MSa and Control Plan - Data management and analysis for the tracking and control of processes ...
processes. Meeting and exceeding requirements of both ISO and internal/external requirements is key. RESPONSIBILITIES - Development and implementation of Quality Tools, FMEA, SPC, MSa and Control Plan - Data management and analysis for the tracking and control of processes ...