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Senior project manager

Solothurn
Michael Page
Director of Projects
Inserat online seit: 21 Januar
Beschreibung

* Prestigious pharmaceutical company
* Temporary assignment for the next 6 months

About Our Client
Our client, an internationally renowned pharmaceutical company is recruiting. On its behalf we are now looking for a Senior Project Manager (m/f/d) for Solothurn area, to join an international team for a period of 6 months with an immediate availability.

Depending on the selected candidate's performance and motivation, there is the possibility of an extension or a permanent takeover.

Job Description
The Senior Project Manager (m/f/d) oversees schedules, meetings, and progress tracking; addresses technical challenges; and ensures structured, well-documented, and coordinated project execution across all phases through the following areas of responsibility:

* Leads and delivers small CAPEX engineering projects from initiation through successful completion
* Provides continuous project and/or construction management support for engineering activities
* Defines project scope, requirements, deliverables, and success criteria
* Develops, maintains, and controls project plans, schedules, milestones, and budgets
* Coordinates and aligns contractors, suppliers, and internal stakeholders to ensure seamless execution
* Oversees on-site activities, ensuring compliance with safety, quality, cost, and schedule requirements
* Proactively identifies risks and issues, implement mitigation measures, and escalate when necessary
* Prepares and presents clear, structured project updates covering status, risks, issues, and next steps

The Successful Applicant
In order to be considered for the role, the selected candidate must have:

* Successfully completed bachelor's degree in engineering (Chemical, Mechanical, Industrial) or Life Sciences (Pharmaceutical Sciences, Biotechnology) or equivalent
* Minimum 5-7years' proven experience as Project Manager and/or Construction Manager supporting small CAPEX projects
* Experience working within a pharmaceutical or biotech manufacturing environment with solid understanding of GMP requirements
* Experience operating in a regulated, internal, and controlled engineering environment
* Fluency in English (spoken and written); additional languages are an advantage
* Ability to work independently while integrating effectively within a multidisciplinary engineering organization
* Strong organizational, planning, and structuring skills with the ability to deliver clear, accurate, and timely project reporting
* Proactive, solution-oriented mindset with strong problem-solving capabilities
* Excellent verbal and written communication skills, with the ability to engage and align internal and external stakeholders

What's on Offer
An ideal short-term opportunity to strengthen your CV by taking immediate ownership of CAPEX engineering projects within a prestigious pharmaceutical company, gaining valuable GMP-regulated experience.

Contact: Christina Beer
Quote job ref: JN

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