a challenging position that will require you to combine strong analytical, managerial, and problem-solving skills. This will be a position of 6 months with the possibility of extension. RESPONSIBILITIES You will oversee the Quality Control of various production
industrial robotsGood knowledge of Siemens and/or Allen Bradley (RA) PLC’sAbility to read and create technical documentation and projectdocumentation including requirement definitions, functional designspecifications and test documentationAbility to produce good quality application software programs for PLC
implementing an innovative best-in-class solution to manage risk in global freight shipment based on seasonal temperature variations. In order to achieve this, data modelling and analysis of large quantities of data is required to detect trends and patterns that could impact product quality. In addition ...
Assurance coordinator you will supervise a team that will be responsible for the quality of all final products. Next to that you will have multiple responsibilities: • Investigate and assess non-conformities • Assess all test results regarding all quality processes and ensure they are aligned with quality
Manager in ensuring GMP & GDP compliance. RESPONSIBILITIES - Ensure that local QA SOPs meet requirements - Support QA Manager with CAPA, root cause analysis, complaint handling, deviation management, change control. - Support QA Manager with release - Manage GDP
within the organisation. - Responsible for audits. - Coordinating and participating in various continuous improvement projects. REQUIREMENTS - Bachelor's or Master's Degree in Food Technology, Analytical Chemistry, Food Quality Management, or similar. - At least 5
department. You will be responsible for safeguarding the quality of the produced goods and working together with teams of other disciplines in order make sure all is compliant. RESPONSIBILITIES - Ensuring all documentation is in accordance with GMP - CAPA, researching
implemented. RESPONSIBILITIES Besides supervising the quality systems you will work with the current team towards strategy targets and maintain a continuous improvement form a quality point of view. Your responsibilities will lay with especially ISO 134845 and internal
Quality a strong voice in the company. You will lead a team of Quality Officers and you will work closely together with the Plant Manager and the Group QA Manager. If you are passionate about leading teams and working towards quality improvement, this is the role for you ...
atmosphere that appreciates hard work and pro activity. ROLE DESCRIPTION This international and quickly growing company is looking for extra hands on the QA department. They are looking for a Quality Assurance Coordinator. You will work
System • Supervising all international standards within the company • Where support is needed support the Quality Control team REQUIREMENTS • A BSc. With at least 3 years’ experience within high tech Medical Devices Quality Assurance • Knowledge of Design Control
patient expectations and ensuring their safety and health. ROLE DESCRIPTION They are looking for someone to join the team that is currently expanding rapidly where you will take on the task to set up the new quality team that will join the
- Responsible for GMP compliance RESPONSIBILITIES - Responsible for Pharma products manufactured in compliance with the GMP - Responsible for the monitoring, control and release of medical devices and Pharma products packaged by our client. - Develop ...
with the Good Manufacturing Practices (GMP). The job holder is also responsible for the control and release of medical devices. RESPONSIBILITIES Responsibility for ensuring that a QMS is established, implemented, maintained, reviewed and continually improved in
RESPONSIBILITIES - Leading the quality management (quality assurance) for the whole site - R&D product licensing - Clinical & non-clinical studies - SOPs - Planning and Execution of Audits - Participation in R&D projects REQUIREMENTS - Degree in
This project is for the time of 1 year with possibility to be extended. RESPONSIBILITIES Besides implementing and monitoring the quality systems you will also be responsible for legal requirements and certification requirements Other tasks related to your role
REQUIREMENTS - 5 years of Experience or more - Experience in a Quality role in Pharma or Medical Devices - Knowledge of GMP and/or ISO standards Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact
Audits en inspecties uitvoeren en ondersteunen - Adviseren over en toetsen op correct gebruik van het kwaliteitssysteem (change control, deviaties CAPA's en klachten) - coördineren van trainingen m.b.t. de toepassing van het kwaliteitssysteem REQUIREMENTS ...