Senior Technician Quality Control - Krefeld, Deutschland - Beckman Coulter Diagnostics

Beckman Coulter Diagnostics

Geprüftes Unternehmen

Krefeld, Deutschland

vor 2 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Wondering what's within Beckman Coulter Diagnostics? Take a closer look.

At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward.

Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates.

Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher.

Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges.

The
Senior Technician Quality Control for Beckman Coulter Diagnostics is responsible for the
release of finished goods in our Manufacturing unit
.

This position is part of the Quality Support Team located in Krefeld, Germany and will be
on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

You will be a part of the Quality Team and report to the Supervisor Quality Control responsible for Quality and Regulatory affair in our manufacturing unit.

If you thrive in a supporting role and want to work to build a world-class Customer Service organization—read on.

In this role, you are responsible:

Release of finished products according to specifications, including in-process controls
Release of raw materials
Calibration and preparation of measuring equipment, use of this measuring equipment in the release processes
Execution of documentation according to GMP/ISO 1348
Maintenance of the specifications.

The essential requirements of the job include:

Reliability and like teamwork.
You have completed training as a pharmaceutical technician assistant, medical technical assistant or comparable training in XXX field 35 year of experience.
You bring good communication skills as well as PC and German/English language skills

It would be a plus if you also possess previous experience in:

Experience in a manufacturing environment/technical service organization ideally in the health care business
Experience with ISO standards, as ISO 13485, GMP, GDP

Der
Senior Technician Quality Control bei Beckman Coulter Diagnostics ist für die
Freigabe von Fertigwaren in unserer Produktionseinheit verantwortlich.

Diese Position ist Teil des Qualitätsteams in Krefeld, Deutschland, und wird vor Ort sein. Unsere Vision bei Beckman Coulter ist es, das Gesundheitswesen von Diagnose zu Diagnose neu zu gestalten.

Sie sind Teil des Qualitätsteams und berichten an den Supervisor Quality Control, der für die Qualitäts
- und Zulassungsangelegenheiten in unserer Produktionseinheit verantwortlich ist. Wenn Sie sich in einer unterstützenden Rolle wohlfühlen und am Aufbau einer erstklassigen Kundendienstorganisation mitarbeiten möchten, lesen Sie weiter.

In dieser Rolle sind Sie verantwortlich für:

Freigabe von Fertigprodukten gemäß den Spezifikationen, einschließlich prozessbegleitender Kontrollen
Freigabe von Rohstoffen
Kalibrierung und Vorbereitung von Messgeräten, Einsatz dieser Messgeräte in den Freigabeprozessen
Durchführung der Dokumentation nach GMP/ISO 1348
Aufrechterhaltung der Spezifikationen.

Zu den wesentlichen Anforderungen der Stelle gehören:

Zuverlässigkeit und Teamfähigkeit
Sie haben eine abgeschlossene Ausbildung als PTA, CTA oder eine vergleichbare Ausbildung im Bereich Qualitätskontrolle mit 35 Jahren Erfahrung.
Sie bringen gute Kommunikationsfähigkeiten sowie PC und Deutsch/Englisch-Kenntnisse mit.

Es wäre von Vorteil, wenn Sie zusätzlich über Erfahrungen in folgenden Bereichen verfügen

Erfahrung in einer Produktionsumgebung/technischen Dienstleistungsorganisation, idealerweise in der Gesundheitsbranche
Erfahrung mit ISO Standards, insbesondere ISO 13485, oder GLP (Good Laboratory Practice) und GDP (Good Documentation Practice)

When you join us, you'll also be joining Danaher's global organization, where 80,000 people wake up every day determined to help our customers win.

As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful
Danaher Business System tools and the stability of a tested organization.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve.

Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you've ever wondered what's within you, there's no better time to find out.