We make it GmbH is a company operating nationally in Switzerland which thanks to many years of successful experience has a high level of expertise in the personnel services sector. Its recruitment activities are focussed on the core areas of industry technology office/administration engineering pharmaceuticals and IT.
We make it GmbH places the highest demands on quality ethics and discretion.
For our client the company CSL Behing in Bern we are looking for a CAPEX Project Manager (m/f/d).
Background
About CSL Behring
CSL Behring is a global biotherapeutics leader driven by its promise to save lives. Focused on serving patients needs by using the latest technologies we develop and deliver innovative therapies that treat coagulation disorders primary immune deficiencies hereditary angioedema respiratory disease and neurological disorders. The companys products are also used in cardiac surgery burn treatment and to prevent hemolytic disease of the newborn.
Tasks
- Responsible for project activities required to scope develop procure construct and qualify new equipment and facilities required to meet facility production throughput demands
- Leads multidisciplinary 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.
Requirements
- 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
- 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
Work hours
- 41 h/ Week
- Remote possible
Are you interested
Then Ms. Emina Becic looks forward to receiving your complete application documents (CV work reference letters and diplomas).
We look forward to hearing from you.