Supplier Quality Data Specialist - Darmstadt, Deutschland - Merck KGaA Darmstadt Germany

Merck KGaA Darmstadt Germany

Geprüftes Unternehmen

Darmstadt, Deutschland

vor 3 Wochen

Geschrieben von:

Lena Wagner

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:

Join us in becoming a member of the global External Supply Quality team, performing our data management activities.

In this capacity, you will manage Supplier Quality data and document, user accesses and digital reporting, that are necessary to monitor manufacturing and development activities.

In collaboration with internal stakeholders, you ensure that supplier and material data is accurate, harmonized, visible and maintained in compliance with Merck standards and expectations.

You will operate workflows in our validated database related to supplier master data, audits and quality agreements.

Reports will be created and generated on our change notifications, risk management and supplier complaints data. You also participate to cross-functional projects and contribute to the continuous improvement of related processes.

You are part of a global team driving Quality and Compliance activities at our manufacturing sites worldwide, with a passion for improving the lives of patients.

The position is limited to one year.

Who you are:

Degree in a relevant discipline
Minimum 2 years in the pharmaceutical of life sciences industry
Strong in Microsoft programs: Excel, Power Point, Share Point, Power BI
Experience in Data Management, and KPI reporting
Administration experience in Track Wise, Document Management Systems
Experience in SAP or other ERP system is a plus
Knowledge of ISO, GMP & GDP regulations
Excellent communications and collaboration skills
Fluent in English. Other languages desirable

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