a strong voice in the company. You will lead a team of 9 QC Officers and you will work closely together with the Site Manager and the Group Quality Manager. If you are passionate about leading teams and working towards quality improvement, this is the role for you. This is a temporary assignment for
Equipment responsibility till successful Run @ Rate. Processes Development - new solutions/processes work with Central Control Engineering team. Support plant MEs in more difficult topics - machine programs modification. Maintain lessons learnt from project launch and production,share globally. Traceability
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 softwareprograms for PLC
PDCA, CAPA) Cost Reduction projects with clients Implementations of new ideas and equipment Organize meeting with Quality Improvements Team Your qualifications We expect that you have at least a Bachelor's degree in Quality Management Lean SiX Sigma certification would be a plus 5 years of increasingly
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
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 ...
In reference of the continuous development of one of our clients, an international producer of the roof systems for automotive industry, OTTO Polska Specialist Staffing is looking for the candidates interested in the job offer: Quality Engineer (automotive) Nr ref.: MD/QEP/01/15 Workplace: Requirements: University degree (quality management, production management, mechanical engineering, commodity studies ...
Australian regulations Manage product releases and process validation in cooperation with Regulatory Affairs department Recommend actions with regards to suppliers' cooperation based on performed audits, risk and compliance assessments Perform quality audits and receive incoming inspections and external
- 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
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
System and negotiate Quality Agreements with third parties. You'll also be responsible for the maintenance and continuous improvement of the local Quality Management System. You'll work with and directly report to the Head of Quality. RESPONSIBILITIES
systems and ISO 13485 norms. As well as internal procedures by proactively interpreting regulatory and quality requirements and determining way of working. • Continuously improving of the quality management system in the company • Secure the functioning of the self-inspection systems
audits, interact with external partners, create Quality agreements... RESPONSIBILITIES - Build up a Quality Management System: ISO9001, ISO 14001 - Conduct information mapping, process writing and perform a strong gap analysis - Implementation of the ISO 18001 in
do quality reviews. Continually you are a part of improving the quality of the products. You will work in a team of QP’s and QA specialists and you are responsible to report to the QP. The end date of this project is not yet known, expected 6-8 months. RESPONSIBILITIES