freiberufler Program Manager auf

Program Manager

  • auf Anfrage
  • 1018 Lausanne
  • auf Anfrage
  • en  |  fr
  • 08.05.2019


Successful design, development and deployment of solutions supporting business setup and transformation in BioPharma and Health Sciences industries. Excellent team leader and player collaborating effectively with crossfunctional teams

Ich biete

  • Agile Entwicklung
  • Business Analyse
  • Confluence (Atlassian)
  • CSV
  • Enterprise project management (EPM)
  • GxP
  • Manufacturing execution system (MES)
  • Pharmaforschung
  • Programm Management
  • Projektleitung / Teamleitung

Projekt‐ & Berufserfahrung

MES Program Manager (Festanstellung)
Nestlé Skin Health, Lausanne
9/2017 – 2/2019 (1 Jahr, 6 Monate)
Life Sciences

9/2017 – 2/2019


Accountable for successful delivery of the MES Program, including planning, governance and overall quality of deliverables. Responsible for coordinating interdependencies between MES work streams, while driving contribution of 5 direct reports, and 60+ other program contributors. Main activities include:
• Define, track milestones and timeline together with other groups within the Spring program and report performance to Senior Management
• Establish Program Budget and implement tools to ensure Cost Control for the overall program
• Ensure program issues and risks are identified, quantified, managed and tracked while communicating them appropriately
• Organize and present regular Program updates to the steering committee and/or management
• Ensure that MES<>SAP interfaces meet business requirements and fully support the company objective of having harmonized MES functions and standard End to End business processes

Eingesetzte Qualifikationen

Projektleitung / Teamleitung (IT), SCRUM, Manufacturing execution system (MES), Gute Herstellungspraxis (GMP)

Project Manager
GSK Consumer Healthcare, Nyon
1/2016 – 8/2017 (1 Jahr, 8 Monate)
Life Sciences

1/2016 – 8/2017


Joined as Project Manager for 3 Manufacturing Information Systems, promoted rapidly through a series of increasingly responsibilities to management positions based on strong reliability, engagement, and team Leadership performance. Managed 7 direct reports progressing 7 IT Manufacturing projects in parallel.
• Ensure re-hosting project activities are compliant with the Global IT standards and regulatory requirements including cGMP and CSV.
• Develop project core team, train, and retain high-quality employees
• Define trackers to measure program benefits and communicate progress to steering committee, management and other stakeholders
• Ensure systems are cutover on agreed dates (plant shutdowns) to avoid the plant paying a monthly high cost penalty to Novartis
• Lead a Task Force aiming at increasing site production performance, with a daily reporting to the Site Leadership Team

Eingesetzte Qualifikationen

Projektleitung / Teamleitung (IT), Enterprise project management (EPM), Computer-integrated manufacturing (CIM), Gute Herstellungspraxis (GMP)

Sr. Business Analyst – Global R&D IT
Elanco, St-Aubin
6/2015 – 12/2015 (7 Monate)
Life Sciences

6/2015 – 12/2015


Lead the integration of GxP systems used by the site (previously Novartis) to Lilly network in partnership with functional areas. Collaborate effectively with Global R&D, Global IT, Quality Systems and the R&D Site Leadership team to deliver integrated technology solutions. Act as CSV manager and expert for the site.
• Educate customers on their new environment and provide customized solutions for complying with new company standards.
• Align and coordinate with Quality and the System Owners for Computerized Systems Validations (CSV) and manage the site Validation Master Plan.
• Serve as a key account manager and contact for various functional areas, working with the business to identify and capture new opportunities, improve processes and optimize the value IT can provide
• Facilitate a collaborative approach that is aligned with Global IT and includes internal & external IT Service Providers

Eingesetzte Qualifikationen

Enterprise project management (EPM), Business Analyse, Gute Laborpraxis (GLP)


Agile Project Management
Jahr: 2016
Ort: Geneva
Project Management Professional
Jahr: 2013
Ort: Philadelphia
Jahr: 2004
Ort: Nancy


PMP Certificate
Scrum Master Certificate
Master Degree of Bioinformatics

Über mich

Work well with virtual, cross-functional teams
Excellent team leader
Available within a month

Persönliche Daten

  • Englisch (Fließend)
  • Französisch (Muttersprache)
auf Anfrage
  • Europäische Union
  • Schweiz
15 Jahre und 9 Monate (seit 01/2006)
10 Jahre


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