Senior Quality Assurance Specialist

2 settimane fa

Milano, Italia Abbott A tempo pieno

Sr. QA Specialist: Job Description Abbott Core Diagnostics in Milan, Italy is looking for a Senior Quality Assurance Specialist.
As a Senior QA Specialist, you will support the whole life cycle of our software products, either In Vitro Diagnostics (IVD) medical device software or non-medical software products.
You will closely work with R&D organization to review and approve all software deliverables, from requirements to design outputs, to test cases throughout all project milestones. After product launch, you will support the Delivery organization being responsible for the quality aspects of products customizations, installations, and servicing activities.
You will also contribute to the Quality Management System documentation maintenance, to nonconformances, corrective and preventive actions processing and to internal and external audit execution.
The ideal candidate has a demonstrable track record in the medical device sector with a focus on software processes, methods, and tools. Proficient English is a must.
Major Accountabilities Participate, as Quality representative, in medical and non-medical products development projects. Supervise quality aspects in products customizations, installation and servicing activities. Create / update Quality Management System (QMS) documentation in accordance with Abbott procedures and applicable regulations, ISO/IEC standards and FDA guidelines. Participate in internal / external audits. Manage non-conformances, Corrective and Preventive Actions (CAPA), customer complaints. Education Bachelor degree in biomedical engineering, Computer science or equivalent.
Required Qualifications / Experience Min 3 - 4 years of experience in Medical Device business sector. Knowledge of ISO 9001, ISO 13485, ISO14971, IEC 62304, FDA 21 CFR Part 820 and related FDA guidelines. Fluent English oral and written. Knowledge of SW development process, techniques, tools. Good knowledge of MS Office products. Preferred Qualifications / Experience Knowledge of ISO 27001 and EU regulations 2017-746 (IVDR) and 2016-679 (GDPR). Skills Attitude to team working and open to multi-cultural environments. Communication, collaboration, and negotiation skills. The base pay for this position is N/A.
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Operations Quality
DIVISION: CRLB Core Lab
LOCATION: Italy > Milan : Viale Edison 110, Edison Park Centre
ADDITIONAL LOCATIONS: WORK SHIFT: Standard
TRAVEL: Yes, 10 % of the Time
MEDICAL SURVEILLANCE: Not Applicable
SIGNIFICANT WORK ACTIVITIES: Not Applicable

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