Aubonne, Vaud, Switzerland
8 hours ago
QA Operations PQR & Complaints Specialist

 

Work Your Magic with us!  

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 


Your role: 

 

Complaints:

Handle customer complaints and coordinate investigations (internally or externally) to ensure that preventive and/or corrective actions are implemented as appropriate.Manage reception and destruction of complaint samplesCoordinate the investigations and write investigational report in the Trackwise systemEnsure adequate CAPA plan is implemented Perform the monthly complaint review reports

 

Product Quality Review (annual product review):

Establish annual plans for Product Quality Review.Coordinate the edition of the annual Product Quality Review for Semi-finished and finished products.Support Continued Process Verification (CPV) activities and provide data to global process owner

 

Other activities : 

Aubonne representative in Complaints and PQR Community of Practice (COP).Subject matter expert for audits and Health authorities inspections 

 

Your Ideal Profile:
 

Master in pharma, biotech or medical devices1-4 years of experience in QA or related fieldExpertise and knowledge concerning our products, a big plusYou are organized, proacvtive and comfortable working with multiple deadlinesYou are a team player, with string collaboration and coordination skills French Fluent, English minimum B2


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!

 

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