With over 2800 Engineers, Sii is the top IT & engineering services provider in Poland. We work with passion for the best companies! At the moment we are looking for:Control Engineer / PLC Programmer City: Gdańsk170407-A9E57 TasksPreparation of technical
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
years experience with Quality Control or in an operational Quality Assurance role. - Experience with HACCP, BRC and IFS. - Fluency in Dutch and English. Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact
possible deviations and providing training on the QMS - Discuss deviations with along the quality lines of the organization and change control - Batch review, audits and guiding inspections REQUIREMENTS - BSc. in a life-science related field, preferably medicine ...
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 ...
external audits by customers and follow up action plans Documentation control and revision on shop floor level Evaluation of the measurement systems and tools Definition and maintenance of visual standards Registering, monitoring and deciding on non-conforming material and products Employer’s offer: Requirements: University degree (quality management, production management, mechanical engineering ...
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
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
effective process that comply to all standards and regulations. RESPONSIBILITIES • Working together with the QA/RA specialist team and ensure a safe process and product at the end of the process • Safeguarding and where needed improving the current Quality Management
- 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
Take over the roles as Quality Management Manager for EU-GMP-guidelines RESPONSIBILITIES - Responsible for medicinal products manufactured in compliance with the GMP - Responsible for the monitoring, control and release of medical devices and Pharma products
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
As an interim QA specialist you are responsible for the routine work of Quality Systems activities. Monitor, review and give advice to your colleagues about procedures and standards of Quality Assurance is a part of your function. - helicopter view in guarding guidelines within QA - Give training
looking for passionate specialists to fully service the customer’s needs. ROLE DESCRIPTION As the new quality Assurance officer you will be an addition to the team due to high growth of the company and need of more specialists within the QA. You