Required education level
Ad. Federal PET / Fed. PET Diploma, Bachelor, Master
Required experience
Between 1 and 3 years
Required language knowledge
English German
Required skills
QA Manufacturing Medical Devices Switzerland MEDICAL DEVICES SWITZERLAND medical devices switzerland FDA Medical devices Audit CAPA manufacturing validation Switzerland vigilance Validation audit Surveillance risk ISO fda Risk MANUFACTURING Audit safety Complaint Vigilance surveillance 13485 14971 root cause Corrective action preventative action tools investigation


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Urgent - Product Engineers (2) - Zurich area MedTech - growing company - English essential with German a bonus

I'm currently on a search for 2 Product Engineers for a Swiss based international Medical Devices manufacturer. Reporting in to the Head of Research and Technology, they will conduct technical investigations, support the regulatory team, author technical documentation and provide feedback to other departments in regard to product performance.

The company itself specialises in the development and sale of respiratory related equipment. Acquired recently by a US based international Medical Devices company, they are up-scaling their operations and with solid financial backing.

Two 2 positions are on offer, meaning there is flexibility to take on a mixture of experience and skillsets, thus an opportunity for both junior and senior professionals to see their career develop in this department.

Key Responsibilities:
 Device inspection and root cause analysis on returned products
 Initiate corrective actions
 Analyse engineering data, test certificates, risk evaluations, and compile trendings of product performance in the marketplace.
 Data analysis and reporting in English

Key Requirements:

 First hand experience in investigating electro-mechanical medical device product issues in the industry down to root cause (complaint handling) and the implementation of corrective actions (CAPA).
 Their products being electro-mechanical in nature means a background/degree in a technical field such as mechanical engineering, electrical engineering or biomedical engineering is relevant, although other backgrounds such as Physics or Quality will be considered, as will a technical apprenticeship with some industry experience in a regulated environment. Validation and Verification experience could also be a good base. We are NOT looking for Software Engineers or testers.
 Good attention to detail, enjoyment from problem solving in a hands on technical environment, and working autonomously and within a team as required
 Fluency in English (written and spoken) with German a plus.

If this sounds like you, please contact me on 0041 43 50 80 816 for a confidential discussion of this (and other suitable) opportunities, and send in your CV in WORD format with employment records (Arbeits Zeugnisse) and Training certifications to

For industry news and new opportunities in QA within the Medical Devices & Diagnostics sectors, please also join my Linked group

KEY WORDS: Quality Assurance, QA, Compliance, Complaint, vigilance, surveillance, safety, Medical Devices, Switzerland, ISO 13485, ISO 9001, ISO 14971, GMP, CAPA, Audit, root cause, trending, risk analysis, Corrective action, preventative action, Production, Manufacturing, Orthopaedics, tools, surgical, navigation, Medical Device jobs, nonstop recruitment

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

NonStop Recruitment
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Contact info

NonStop Recruitment
Andrew Boroky
10w yw y- z7 )y( 07g
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