Quality Assurance Engineer İş İlanı
İşveren Hakkında
QUALIFICATIONS AND JOB DESCRIPTION
Qualifications:
- Bachelor degree in Engineering and technical or Health/Life Sciences departments of universities.
- Min 2 years of experience in Quality Management Systems preferably in Medical Devices Industry
- Good command of English is compulsory, German knowledge would be an asset
- Knowledge of tools/ methodologies such as design control, risk management, root cause investigation methods, process validation, statistical process control (SPC), protocol/ report preparation.
- Knowledge of ISO 13485, European Medical Device Regulation and FDA 21 CFR 820 requirements, understanding the medical device regulatory environment and requirements
- Knowledge of ISO 11135, ISO 11137, ISO 11737-1, AAMI ST72 etc. related EO/Gama Sterilization, Bioburden, LAL and Envoiremental Monitoring System regulations
- Familiar with QMS processes like Technical File preparation, CAPA, Complaint management, document control, internal audit etc.
- Good knowledge of MS Office applications is required and SAP is an asset
- Statistical data analysis, documentation and report writing skills
- Internal auditor certification preferred
- 6 Sigma certification preferred
- Exceptional analytical, problem solving & root-cause analysis skills
- High level of attention to details and accuracy
- Excellent communication skills, ability to work in a team environment and lead a project team
- Ability to lead or work with multi- departmental project teams and resolve quality related issues in a timely and effective manner
- Be self-motivated, self-starter, be able to meet deadlines, be a good team player, be able to assist and support others
- Result oriented
- Be open-minded and willing to learn
- Ability to travel as required
Job Description :
For Quality Assurance Engineer position, four colleague will be hired and assigned to the appropriate main groups of Quality Management System listed below.
The person who hired will be responsible one or several processes in assigned group.
Quality Assurance
- Non-Conforming Product Management with using QDMS
- Product Release
- Control and approval of laboratory routine test results
- Rework Process
- HHE,FSCA, Hold processes
- Customer Complaint Handling Management with usign TrackWise
- Customer Complaints Reporting Process
Design Quality
- Computerized systems validation
- Control and approval of validation studies (Process, test method etc.)
- Control and approval of Receiving Inspection plans
- Control and approval of label designs/layout
- Control and approval of Technical File Content
- Monitoring and organization of Quality responsibilities in Change Management System
- Design quality assurance processes
- Control and approval of calibration forms
Compliance
- Management of Corrective and Preventive Actions with usign TrackWise
- Internal audits with using QDMS
- Management of Document Control Process with using QDMS
- External audits
- QMS statistical analyzes
- KPIs / Quality Objectives
- Quality Management System Plans
- Implementation of Global Procedures
- Environmental Management System Compliance
- Quality Management System trainings with using LMS
Quality Assurance – Supplier Controls
- Supplier audits (global and local)
- Control and approval of supplier qualification
- Control and approval of the approved supplier list
- Trend and support of SCAR
- Control and approval of supplier evaluation
- Controlling the preparation and signing process of supplier contracts
- Follow-up of supplier-sourced changes
- Support to the supplier-sourced nonconformity management process
Quality Assurance - Sterilization & Laboratory
- Control and approval of laboratory and cleanroom validation/qualification studies
- Supporting the creation of laboratory microbiological (BB-LAL-environmental) and chemical (EO/ECH) test methods and programs
- Control and approval of internal and external sterilization validation/qualification studies
- Communicating and collaborating with external sterilization suppliers and test laboratories
- Follow-up and support of routine sterilization activities
- Annual laboratory and sterilization reviews
- Cleanroom conformity assessments
- Determining the hygiene specifications and rules of the areas and ensuring that these rules are followed
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