For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort unbefristet
eine/n
Wissenschaftler (m/w/d)
Unterstütze uns bei:
1. der eigenständigen Einleitung, Durchführung und Betreuung von Transfer & Validation Aufträgen
2. der Verbesserung der bestehenden Methoden und Ablaufe
3. die Etablierung von neuen Methoden und Verfahren
4. den Laborarbeiten mit GVOs und Biostoffen bis hin zur Risikogruppe S1
5. bei der Bearbeitung von internen Dokumenten wie BOPs und Laborablaufplänen
6. der Erstellung von Auswertungs- und Trackingsheets mit Hilfe von Excel oder Smartsheet,
7. der eigenständigen Überprüfung von Labordokumentation sowie der Auswertung und Zusammenfassung von Analyseergebnissen
8. der Organisation und Pflege der Analysendaten in einer Datenbank in Verbindung dem LTM (Laboratory Testing Management) System
9. der Betreuung des technischen Personals bei der Durchführung von Analysen
10. der Zusammenarbeit mit in- und ausländischen Kunden
11. der Bearbeitung von wissenschaftlichen Fragestellungen, Kundenanfragen sowie Freigabe von Analysenergebnissen
Überzeuge uns durch:
12. Ein abgeschlossenes Studium der Naturwissenschaften oder vergleichbare Qualifikation
13. Wissenschaftliche Expertise (praktisch und theoretisch) im Molekularbiologischem Bereich speziell im Bereich PCR und real time PCR
14. Sehr strukturiertes, detailorientiertes und zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien
15. Wünschenswert wären Erfahrungen mit Tiermodellen
16. Service und Kundenorientierung
17. Sehr gute Kenntnisse von Microsoft Office sowie gute Deutsch- und Englischkenntnisse
Wir bieten Dir:
18. Eine Vollzeitstelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
19. Eine intensive Einarbeitung
20. Flexible Arbeitszeiten
21. Eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
22. Eine angemessene Vergütung
Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 233344 über unser Karriereportal mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!
Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15 A-B
40699 Erkrath
Job Description
Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Executes scientific testing strategies and studies. May participate in development as part of team. May lead assay research, assay validation or study conduct, or is involved in preparation of material (e.g. protein, nucleic acid, cells, etc.). Reviews and interprets study data, communicates results to clients and writes final reports. Ensures compliance with protocols and all applicable SOPs. Troubleshoots and resolves assay or technical issues in the laboratory when scientific expertise is needed. Contributes to specific dataset interpretation, or when appropriate answering questions from regulatory authorities. For singular focus of Chemistry or Biology disciplines, refer to specified role on job architecture.
Education
Four-year degree required
Physical Requirements
About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.