Beschreibung
For our client, a worldwide leading MedTech company, we are looking for aConsumables Manager (m/w) 100%
General Information:
- Start date: 17.08.2020
- Latest start date: 01.09.2020
- End date: One year contract
- Extension: Yes
- Team: 12 Peers
- Workload: 100%
- Remote/Home Office: No
- Traveling required: Yes / 10 – 15 % / EU / USA
Tasks & Responsibilities:
As Technical Consumables Manager you have the responsibility for one or several Consumables Products where you are responsible for:
Quality:
- Ensure regulatory compliance during product care
- Acting as point of contact for Regulatory when supporting country specific registrations with additional documentation
- Investigation unit for complaint handling and coordinator for resulting CAPA's and SCAR's
- Coordinator for incoming goods issues and "IF" issues reported by suppliers
- Responsible for technical specifications and evaluations in the RfQ process for investment projects in the product care phase
- Support Global Audit Team with preparing and executing supplier audits
Finance:
- Budgeting for Standard Manufacturing Cost, one time period cost and Product Care activities
- Collaboration with procurement to ensure production capacity related to available forecast
Projects:
- Initiating product care projects as sponsor for invest projects, process and product improvement projects and obsolescence projects
- Product Care representative in development projects
Change Management:
- Responsible for evaluation of change requests from suppliers
- Change manager for approved changes
- At least 5 Years of experience
Interfaces:
- Acting as Consumables representative in instrument Product Team Meetings, System Development organization and Product Care Quality Teams related to the Consumables portfolio (Communication typically in English)
- Point of contact for suppliers to all aspects not related to purchasing (Communication typically in German)
Must Haves:
- Completed university studies (e.g. mechanical engineering, automation technology/materials engineering) or comparable higher education in a technical and analytical field with experience in the medical field, especially in in-vitro diagnostics
- Experience in regulated product development in cooperation with international stakeholders
- Experience in project management with external partners/suppliers
- Technical manufacturing experience with high level of automation
- Continuous improvement processes and statistical analysis
- German and English - Proficient
Nice to Haves:
- High degree of assertiveness, dialogue skills and team orientation personality
- Responsibility for results & proactive and integrative approach
- Willingness to travel (approximately 10-15%)