Consumables Owner.

Are you great with IVD product management and production engineering, Do you have expertise in Process Management methodologies and in-vitro diagnostic-related regulations?  Do you have profound experience in IVD product development? 
Do you want to be a part of a world-leading pharmaceutical company? Then have a look at the job description below  

Tasks & Responsibilities:

• Accountable for assigned product(s)
• Accountable for Product- /Production-issues and risks
• Owner of product specification and production process specification
• Accountable for product changes, complaints, and deviations
• Accountable for spare part management
• Accountable for production assets and equipment
• Accountable for the overall Squad performance w/r to quality, supply, compliance, cost
• Ensures a clear, strategic Squad view on prioritization 
• Develops and implements the product-wide production capacity plan and output report in collaboration with the relevant functions in accordance with the Product Strategy and provides information to Network Lead
• Acts as the final decision maker within Squad e.g. prioritization
• Manages all key stakeholders at the Squad level (internal and external)
• Represents Consumables in Business Teams on PCQT level, represents Consumables in system development projects
• Interacts with business (e.g. IPM) to understand demand forecast, its development and fluctuations, and triggers follow-up actions
• Compiles Annual Product Review Report in collaboration with all relevant stakeholders, including triggering actions, risks, and mitigations
• Chairs Product Meetings with suppliers and sub-suppliers at an operative level
• Chairs the Squad and provides the necessary leadership to the team members to assume their accountabilities
• Responsible for Squad budget (e.g. OPEX/CAPEX, development budget, PCQT budget)
• Manages SMC cost account including budget planning and search for potential savings
• Provides feedback to Chapter Leads on Squad Members
• Executes Operatives Risk Management
• Plans replacements and new investments and calculates business cases
• Understands contracts with suppliers as regards of content
• Monitors the supplier safety stock target and Roche hub targets
• Owns and maintains product documentation during the Product Life Cycle

Your profile :

• University degree in Engineering, Natural Science, or related disciplines
• Min. 3 years of work experience in IVD product management and production engineering 
• Knowledge of Process Management methodologies (Lean, Six Sigma, etc.) and in-vitro diagnostic-related regulations, such as ISO 13485, IVDR, FDA 21 CFR part 820, etc. 
• Experience in IVD product development following design control, manufacturing, and testing 
• Leadership skills including the ability to get things done with a proven track record of consensus building and conflict management in challenging situations, eg. in a project leader role 
• Ability to think strategically and systemically, willingness to try new ideas and participate in changes
• The self-motivated, autonomous, structured, and goal-oriented mindset with a solution-oriented balance of short-term mitigation and long-term solution
• Ability to effectively communicate with all levels of the organization by establishing credibility and building rapport
• Executive presence, performing well under pressure, and decisiveness
• Excellent communication skills in English and min. good communication skills in German

We are looking for your applications, Good luck