QA OPS Support - All Genders
QA OPS Support - All Genders
QA OPS Support - All Genders
QA OPS Support - All Genders
Merck
Pharmazeutische Produkte, Arzneimittel
Corsier-sur-Vevey
- Art der Anstellung: Vollzeit
- 89.500 CHF – 105.500 CHF (von XING geschätzt)
- Vor Ort
- Zu den Ersten gehören
QA OPS Support - All Genders
Über diesen Job
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 a member of the QA Operations Technical/Support team for the Warehouse, Equipment & Maintenance (E&M), Dispensing, Data & Digital departments, you will support activities linked to Quality Assurance for these departments.
You Will Be Responsible For:
- Acting as the QA point of contact for deviations, Critical Control Points (CCP), and Corrective and Preventive Actions (CAPA).
- Participating in QA on-the-floor activities to ensure compliance with regulations related to these departments.
- Reviewing, approving, and following up on current Good Manufacturing Practice (cGMP) documentation.
- Participating in health authority inspections and audits.
Your Profile
- Degree in Pharmacy, Engineering, or an equivalent field of study.
- At least 5 years of experience in the pharmaceutical or biopharmaceutical industry in GMP manufacturing.
- Excellent knowledge of Good Manufacturing Practices (cGMP) and Good Distribution Practices (GDP).
- Good knowledge of biotechnology processes.
- Strong analytical skills and experience with investigation tools (e.g., 6M, 5 Whys).
- Proficient knowledge of pharmaceutical and computerized systems (e.g., Trackwise and SAP).
- Excellent proficiency in both French and English.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!
Gehalts-Prognose
Bewertung von Mitarbeitenden
Gesamtbewertung
Basierend auf 1.000 BewertungenVorteile für Mitarbeitende
Flexible Arbeitszeiten
Home-Office
Kantine
Restaurant-Tickets
Kinderbetreuung
Betriebliche Altersvorsorge
Barrierefreiheit
Gesundheitsmaßnahmen
Betriebsarzt
Training
Parkplatz
Günstige Anbindung
Vorteile für Mitarbeitende
Firmenwagen
Smartphone
Gewinnbeteiligung
Veranstaltungen
Privat das Internet nutzen
Hunde willkommen
Unternehmenskultur
Unternehmenskultur
1000 Mitarbeitende haben abgestimmt: Sie bewerten die Unternehmenskultur bei Merck als modern.Dies stimmt ungefähr mit dem Branchen-Durchschnitt überein.