Clinical Materials Coordinator

Aargau  ‐ Vor Ort
Dieses Projekt ist archiviert und leider nicht (mehr) aktiv.
Sie finden vakante Projekte hier in unserer Projektbörse.

Beschreibung

Clinical Materials Coordinator (m/w/d)- SAP/supply chain/ healthcare/English /German

Project:
For our customer F. Hoffman La Roche in Kaiseraugst we are looking for a Clinical Materials Coordinator

Background:
The Clinical Materials Coordinator (CMC) leads the coordination and execution of all procurement activities of drug products for global clinical studies. Furthermore, the CMC is responsible for all tasks related to the goods receipts of drug products. This includes the coordination of the release of these materials to ensure a timely production and delivery of Investigational Medical Products to Roche depots in accordance with international standards and regulatory requirements.

Perfect candidate:
The ideal candidate has excellent written and oral communication and negotiation skills in German and English, is an open-minded, self-motivated, quick thinking, proactive, and customer-focused individual with work experience and knowledge of SAP.

Main responsibilities:
- Compile product-specific data and documents for drug products
- Define, request and continuously update the master data of drug products in SAP-systems
- Manage purchase orders for Roche development drug products, Roche commercial drug products and external commercial drug products from internal and external suppliers in various systems
- Supplier relation management: Manage various drug product suppliers of PTDS (incl. creating suppliers performance transparency with KPIs and taking applicable actions for continuous improvements) and ensure that drug products are delivered according plan / need
- Perform goods inspection and goods receipt of incoming drug products from various suppliers in Kaiseraugst, as well as virtual goods receipts in SAP
- Manage the compilation of a GMP- and customs-compliant goods receipt dossier for the QA-release of drug products
- Request and continuously update GMP- and non-GMP-batch data of drug products in SAP
- Ensure the QA-release or AFM ("Authorization for Further Manufacturing") of drug products on time
- Drive and lead the issue- and GMP-deviation management for global clinical supply concerning the procurement of drug products as well as the goods receipt of drug product
- Provide and maintain safety data and appropriate protective measures for all materials to ensure employee health
- Actively support the Lean Production System (LPS). Establish new processes and improve existing processes in Clinical Supply (Lead and participate in projects to optimize Clinical Supply)

Requirements:
- Associate level of professional education or University degree preferably in Supply Chain Management and/or Healthcare Management.
- Excellent written and oral communication in German and English
- Work experience in GMP environment, supply chain, life science, industrial engineering or equivalent is beneficial.
- Ability to work independently. Self-motivated, proactive, quick thinking, adaptable and well-organized individual. Ability to set priorities and to remain flexible in stressful situations
- Excellent team player with a high level of communication and negotiation skills
- Customer-focused, ability to create trustful relationships with business partners
- Demonstrated problem solving and decision making skills
- Project management skills and experience in lean tools application is beneficial
- Knowledge of SAP R3, APO knowledge is beneficial

Reference No.: 919253SGR
Role: Clinical Materials Coordinator
Industry: Pharma
Location: Kaiseraugst
Workload: 100%
Start: 11.05.2020
Duration: 12++

Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. If the position is not a perfect match and you wish to receive other opportunities directly, you can send us your CV anyway via this advert or to jobs[at]itcag[dot]com.

Contact us for further information regarding our company, our positions or our attractive payroll-only-program: .
About us:
ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
Start
05/2020
Dauer
12++
(Verlängerung möglich)
Von
ITech Consult AG
Eingestellt
16.04.2020
Projekt-ID:
1919980
Vertragsart
Freiberuflich
Um sich auf dieses Projekt zu bewerben müssen Sie sich einloggen.
Registrieren