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Senior Project Manager Engineering Services - Switzerland  

Celgene (company)

Posted on : 08 March 2017

Project Description

  • The Senior Project Manager is responsible to manage projects at an operational and strategic level. 
  • The project manager has the overall responsibility to achieve the project objectives regarding functionality, GMP & EHS compliance and compliant with the respective regulations within approved scope, budget and schedule.  

 Skills/Knowledge Required  
  •  + 15 years of work experience in engineering project management, including 10 years in a pharmaceutical production environment 
  •  Proven success in managing large projects 
  •  Able to contribute to a project from concept phase to full implementation 
  •  Experience with regulatory agencies including FDA , EMEA and other Health Authority agencies 
  •  Solid knowledge in process technologies (solid dosage forms, packaging &) 
  •  Solid knowledge in technical infrastructures (HVAC, utilities,...) 
  •  Solid knowledge in the validation of procedures and systems. 
  •  Fluent in English and French 
  •  Excellent communication and interpersonal skills, strong presentation skills in both small and large group settings and with all hierarchy levels 
  •  Excellent organizational skills 
  •  Ability to take decision 
  •  Knowledge of most common office software (MS Office, MS Project, Autocad)

QualificationsDuties and Responsibilities  
  •  Responsible for the management of multidiscipline projects 
  •  Accountable for project initiation, planning and for overseeing project execution, implementation and closeout. 
  •  Develop the project scope, define project guidelines, prepare project funding requests and coordinate the resources necessary to successfully complete the project. 
  •  Direct multi-disciplinary project teams to ensure delivery of the project on time, on budget and to the level of quality expected by the customer. 
  •  Plan and track budget and timelines. 
  •  Identify potential project risks, provide continuing direction to the project team and conduct regular status meetings to review project activities. 
  •  Manage technical, quality and compliance aspects of the project. 
  •  Coordinate the various phases of the project: construction as well as the acquisition, FAT, 
  •  installation, SAT and commissioning of equipment. 
  •  Responsible for the hand over including documentation to production. 
  •  Follow-up on good operation of building and equipment 6 months after hand-over. 
  •  Ensure adequate report of the project status to the clients. 
  •  Represent the project internally and to externally to authorities. 
  •  Adheres to all applicable company procedures and policies and any other regulatory requirements related to the Pharmaceutical Industry (GMP, etc.). 
  •  Promotes a company culture centered around Health & Safety to all employees and encourages them to maintain a safe and secure work environment at all times.

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