Capex Program / Project Manager

Job description:

Your Mission:

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

Set up a program of projects that all aim to resolve safety gaps

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

About the customer:

For a leading global biotherapeutics company, we are looking for a seasoned Projet Manager Engineering with the focus on managing major capital projects in the pharmaceutical industry. You will be working on projects in field of process safety improvements (fire safety upgrades, etc.), someone who understands these type of improvements, but does not need to be an expert.

• Location: Bern, Switzerland
• Start date: ASAP
• Duration: 12 months (with possible extension)
• Workload: 100% (41h/w)
• Contracting via Swisslinx

Requirements:

Your Profile:

10+ years of experience in managing major capital projects in the pharmaceutical industry

Successful studies in Engineering, Business Administration or Life Sciences (MS/MBA/BS/BA or equivalent)

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

Fluent in both German and English, in verbal and written

Online Application

Are you ready to make some real impact? We are looking forward to your latest CV and your earliest start date. If your profile has been selected for the further steps, our consultant will contact you for a first interview.

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