Quality Technician in Ecublens

veröffentlicht
Kontakt
Jean-Baptiste Masson, Genf Professionals Health Care & Life Sciences
Jobtyp
Permanent
jetzt bewerben

job details

veröffentlicht
Ort
Ecublens, Waadt
Sektor
Life Sciences
Jobtyp
Permanent
Referenznummer
12822
Kontakt
Jean-Baptiste Masson, Genf Professionals Health Care & Life Sciences
Telefon
058 201 54 40
jetzt bewerben

Stellenbeschreibung

Symetis SA, a Boston Scientific Company, develops and produces innovative, minimally invasive heart valve replacement devices. They are today looking for a:

Quality Technician

ROLE PURPOSE: The Quality Technician is responsible for apply quality techniques to ensure the good performance of the medical devices manufactured by the company. Controlling closed Exception Reports/Non-Conformances Reports, Line Audits & Non-Conforming Report Board Reports that are generated. Compiling Non-Conformance Board Reports monthly & various documents for Management on an ad hoc basis. Carrying out Plant-wide Internal Audits & Internal Audits as per relevant schedules. Compiling Yield & Scrap Reports for area.

TASKS AND RESPONSIBILITIES: • Review and update of Quality Documentation. • Routine final functional testing, product release criteria testing/inspection and recording of test results. • Compliance to all Quality Laboratory and all relevant plant wide procedures and practices. • Compliance to all ISO9001 and current GMP procedures and practices. • Provision of excellent service to all internal customers. • Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager. • Decision making ability coupled with the ability to work on ones own initiative and with minimum supervision is required. • In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

YOUR PROFILE (EXPERIENCE, SKILLS, EDUCATION):

• Degree in technical area (mechanical, life science, physics) • 3 years of experience in Medical Device industry • Experience in Catheter and Heart manufacturing would be ideal • Experience in FDA regulatory industry is desirable • Knowledge and application of measurement and tests (caliper, micrometer, destructive and non-destructive mechanical testing) • Experience with internal audits • Excellent analytical, system analysis and problem-solving skills; has the ability to acquire new skills quickly and thrives in a fast paced, collaborative team environment • Ability to recognize exceptions to documented policy and procedures • Ability to monitor schedule deviations and assist in the development of alternative methods for corrective action at the project level • Fluent in French and English