Associate Manager, Product Lifecycle Management

Req #: 1803564
Location:Boudry, NeuchatelCH
Job Category:Manufacturing/Technical Operations
Work Location: Route de Perreux 1 BOUDRY 2017
Organization: Celgene International SaRL
Schedule:40
Shift:
Employee Status: Full time
Job Type: Regular
Job Level:
Travel:
Other Locations:Switzerland- Boudry

Description

Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, ​quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.

2. Skills/Knowledge Required

• General understanding of relevant activities in manufacturing, regulatory affairs, logistics, and of GMP/GDP guidelines, artwork /labeling development a plus


• Ability to lead project teams and timelines successfully


• Ability to work effectively with groups in other geographical locations


• Has a successful track record of leading and accomplishing complex projects internationally


• Be a team player and work in an international environment


• Able to work with independently, partner effectively with other functions at global level, and to set and manage own objectives.


• Ability to challenge status quo, is comfortable with the unknown, results oriented


• Experience in process improvement and understanding of Lean methodology are a plus


• Limited Supervision: Determines own methods to accomplish work. Able to respond independently to majority of complex problems on own.


• English and French required

3. Duties and Responsibilities

Product Launches & Labeling Variation Implementation  

• Project management lead for launch execution activities, working cross-functionally with Regulatory Affairs, Manufacturing sites, Quality, Global Supply Planning, Demand Planning and other operations departments to ensure launches are completed successfully & compliantly by the requested launch date.


• Lead labeling variation projects, cross-functionally, ensuring new label implementations on time and compliantly in the relevant markets


• Identify business needs where needed and propose solutions


• Analyze and provide guidance to commercial teams and affiliates for country specific requirements and verify that they’re in line with the current Celgene Supply Chain strategy. Must also ensure that requirements are implemented in compliance with GMP guidelines and registration dossiers.


• Be an active member of global commercial launch teams (where relevant) and TCT Technical Commercialization Teams contributing to new product launch plans, SKU strategies and other particular product or labeling specific requirements.


• Track launches and variations and issue relevant KPIs

Supply Chain Projects

• DigiCAM (Celgene’s artwork approval management system): participate in change projects to update & / or improve the system’s functionality.


• Participate in projects relating to process improvement around master data, eQRMS change control, artwork approval, clinical trial supply


• Participate in and/or lead projects linked to Brexit, SKU definition, region-specific projects


• Represent PLM in internal risk assessment projects as needed and coordinate implementation of resulted actions

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