Specialist New Product Introduction (M/F/D) 100%

The Specialist - New Product Introduction is a key member of the Product Portfolio Management Team, reporting to the New Product Introduction Lead. This role involves collaborating with cross-functional teams, conducting data analysis, implementing processes, and ensuring successful project outcomes for international (ex-US) new product launches. The specialist will work closely with various departments, including Human Health, Supply Planning, Demand Management, Fulfilment, Market Planning, Regulatory Affairs, Artwork, Serialization, Master Data, Finance, Logistics, and Quality.

• Employment type: Temporary via nemensis ag, 100%
• ID: 21511
• Duration: 15.07.2024 - 14.07.2025
• Salary: CHF 7300.- - 8.900.-/mt
• 2 days of home office

Responsibilities

• Leading cross-functional teams, managing complex information flow, coordinating, and integrating the functional/tactical project management activities for New Product Introduction, in close collaboration with Value Chain Management, Global Launch Planning, and partner with E2E Planners, other Supply Chain functions, and stakeholders across divisions (GHH & MRL).
• Coordinate activities to mitigate risks related to the different milestones across the New Product Introduction stages including, but not limited to: PLR Approval, Code Creation, Initial RCT update, Forecast Positioning, Artwork Readiness, First Packaging, in line with the Health Authority Approval to guarantee successful launches by ensuring system readiness to allow MMD execution.
• Responsible for and providing end to end visibility for New Product Introduction within assigned product portfolio to all stakeholders throughout all divisions.
• Coordinate activities to mitigate risks related to Artwork Readiness. Liaise with Regulatory Affairs, Artwork Centers, and Quality for timely execution
• Drive process improvement initiatives when needed
• Track, and report KPIs mitigating risks to minimize impact on business; participate and provide input to the IBP process (Demand Reviews, Site Supply Reviews).
• Understand & translate the packaging lead times, capacity issues, process reliability issues, sourcing flows, market specific requirements (e.g. TOI, shelf life requirements, etc.) and regulatory issues impacting supply into appropriate risk mitigation actions

Requirements

• Bachelor's degree in supply chain, pharmaceutical sciences, business administration, or a related field.
• 1 to 3 years of experience in the biopharmaceutical industry, with exposure to new product introduction, project management, or related roles.
• Basic understanding of pharmaceutical product development processes, regulatory requirements, and commercialization strategies.
• Strong organizational and task management skills, with the ability to prioritize and meet deadlines.
• Proficiency in data analysis tools and techniques.
• Effective communication and interpersonal skills, with the ability to work collaboratively with team members and stakeholders.
• Proficiency in Microsoft Office Suite and other relevant software.
• Proficient in the use of business software (including MS Excel, MS PowerPoint, MS Project).
• Working knowledge of SAP and Rapid Response (prior experience with Merck MRP systems, practices/principles beneficial).
• Fluent in English.
• Basic understanding of Operations, Planning, Regulatory strategy, and Business/Financial acumen beneficial.
• Pharmaceutical experience is an advantage

Benefits with nemensis ag

• Nemensis ag is your specialized personnel recruiter in Life Sciences based in Basel.
• Comprehensive consulting and support during the application process through our consultants.
• Access to a large network of clients and exciting positions in Northwestern Switzerland.
• Quick and uncomplicated entry through individual guidance and support during the application process.

Sounds like you? Then let's go, I look forward to your application!

Contact: Annika Schelp, E-Mail schreiben