Cell Chain Manager

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

Beschreibung

Job Title: Cell Chain Manager
Position Purpose:
Perform system support (master data management, process support, testing, validation, documentation and training) regionally for the efficient, effective operations of CellChain and for all internal and external stakeholders.
Major Accountabilities
* Perform CellChain support for user management, master data management and change control.
* Build user adoption and expertise in utilizing CellChain to enhance customer engagement and supply chain performance.
* Develop and implement CellChain continuous improvement opportunities.
* Participate in country launches including corresponding site set-ups and user account set-ups in support of all commercial and clinical launches.
* Engage in the short and medium term operational strategy for CellChain with a focus on:
o Scaling the business - Customer engagement, New Clinical Trials, Commercial PedALL, DLBCL, Country Launches, New Treatment Sites, New Manufacturing Sites.
o Maintaining COI
o Maintaining Computer System Validation
* Support CellChain system releases performing PQ testing, change control impacts, user training and procedure updating.
Key Performance Indicators
Implements technology solutions that drive performance in the following Supply Chain KPI's:
Application performance: Application availability, Robust Validation Strategy Data Accuracy: Master Data set-up, user account set-up, Data associations Resource utilization: Timeliness and quality of new treatment site and manufacturing site set-ups
Quality: data setup first-time-right
Front Line Support: User engagement, user satisfaction, escalation as needed HSE (Occupational Accident Rate)
Minimum Requirements
*University Degree in supply chain management or operations. The following certifications a plus: APICS CSCP, CPIM English
* Supply chain system experience with SAP ERP and SFDC CRM applications. Experience with GxP Validated systems. International experience a plus.
* Experience in a cGMP manufacturing environment. Experience in supporting 21CFR Part 11 Computer System Validation and HIPAA regulations.
* Broad general business knowledge with experience collaborating with and supporting multiple functional areas, such as commercial, finance, quality, regulatory, compliance, IT and manufacturing.
* FDA Audit participation experience.

Additionally:

*Candidates who are customer-focused and have pharma industry experience (ideally big 4 pharm.) & Master Data exp. in SAP & Salesforce.

Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Start
09/2020
Dauer
7 months
Von
Michael Bailey Associates
Eingestellt
12.08.2020
Projekt-ID:
1955764
Vertragsart
Freiberuflich
Um sich auf dieses Projekt zu bewerben müssen Sie sich einloggen.
Registrieren