Engineering Project Manager (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

• Responsible for project activities required to scope, develop, procure, construct and qualify new equipment and facilities required to meet facility production throughput demands
• Leads multi-disciplinary Teams through project life cycle activities to deliver capacity expansion capabilities to meet global and local strategic requirements
• Develops and maintains integrated project plans and monitors project activities for adherence to milestone timelines, deliverables and budget against approved plan.
• Develops risk mitigation strategies.
• Ensures that initiatives are aligned with the business objectives and strategic philosophy
• Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval
• Responsible for generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for site Sr. Management and Global Steering Committees
• Project Teams are responsible for completion of project lifecycle activities through performance qualification
• Influences teams to work collaboratively, to be customer focused and to deliver superior performance through personal leadership abilities, mentoring and effective communication.

• Successful studies in Engineering, Business Administration or Life Sciences (MS/MBA/BS/BA or equivalent)
• Solid experience in managing major capital projects in the pharmaceutical industry
  
• Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility
• Excellent understanding of project management principles and project lifecycle phases, including knowledge of Validation, CMC and facility regulatory submission requirements
• Experience to manage high level project budgets
• Ability to handle many tasks simultaneously and integrate project planning efforts across functions
• Ability to understand the big picture and approach problem solving in a proactive team manner
• German knowledge is mandatory

• Varied work in a renowned company
• Pleasant working atmosphere
• Support throughout the entire application process
• Look forward to working in an international environment

Ihr Kontakt

Ansprechpartner
Sandro Frei

Referenznummer
865163/1

Kontakt aufnehmen
E-Mail: sandro.frei@hays.ch

Anstellungsart
Freiberuflich für ein Projekt