QA Engineering Expert - Aubonne, Schweiz - Merck KGaA

Merck KGaA

Geprüftes Unternehmen

Aubonne, Schweiz

vor 2 Wochen

Geschrieben von:

Lena Schneider

beBee Recruiter

Beschreibung

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:

As QA Engineering Expert, you will ensure the quality oversight of all Technical Services activities impacting the different Departments in the Aubonne Site (engineering, qualification, maintenance, calibration...) related to Facility, Utilities, Equipment and related Computerizes Systems used within manufacturing area and in laboratory.

You will guarantee that all related documentation is compliant with GMP norms and other regulations.

As such, you will ensure quality oversight of projects, quality review and approbation of qualification and validation documentation (plan, protocols, reports, deviation...).

Finally, you will manage quality oversight of all compliance aspects related to qualification and validation activities considering these Area (change control processes, deviations, capa).

Your Ideal Profile:

Background or education in engineering (or similar)
Excellent knowledge in CSV (Computerized System Validation)
Relevant professional experience in a pharmaceutical company in Validation area or as a consultant
Experience in Quality assurance in a GMP environment
Experience with audits and inspections
Collaborative with good communication skills
French fluent, English minimum B
You are open for the fresh ideas and new perspectives
Willingness to set yourself challenging goals and develop yourself in order to achieve superior performance
You take initiative to constantly improve products, services, processes and working routines.

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