Engineering Capex Project Manager – Safety focus – 6621 URA
Our client is a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation disorders, immunological diseases, enzyme deficiency diseases and other rare diseases.
Our client is current looking for a experienced CAPEX Program / Project Manager for projects aiming to resolve safety gaps. The projects in this department is in the field of process safety improvements, fire safety upgrades, etc. We are looking for a Capex program / project manager, who understands (does not need to be an expert) these type of improvements.
This role is a initial 12 months contract to be based in Bern, Switzerland with good chances of extension.
Main Responsibilities:
* Set up a program of projects that all aim to resolve safety gaps
* 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.
* Maintain oversight on project risks and 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 implementing EHS by design principles in the project
* 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.
Qualifications and Experience:
* Relevant Swiss working/residency permit or Swiss/EU-Citizenship required
* Successful studies in Engineering, Business Administration or Life Sciences (MS/MBA/BS/BA or equivalent)
* More than 10 years of experience in managing major capital projects in the pharmaceutical industry
* Ideally experience of program management
* 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 is mandatory
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