CAPEX Project Manager

vor 3 Wochen

Bern, Schweiz Proclinical Vollzeit

Are you ready for a change? Tired of the same routine? Join our team and make your mark in the industry
Have a look below and apply or send me your CV directly.

Proclinical is seeking a CAPEX Project Manager with an Automation Background for a temporary contract position of 12 months based in Bern, Switzerland.

Join the team and be part of an innovative company that values inclusion, growth, and impact. This company have a dynamic work environment offers brilliant opportunities for advancement. They are seeking talented and driven individuals who share our passion for making a difference within the Life Science industry.

Responsibilities:

CAPEX Project Manager with automation background We are looking for a Project Manager with experience in leading CAPEX projects in a GMP environment and having specifically a strong understanding of automation systems. Please see also below Job description. Leading CAPEX projects having their focus on automation systems, that will be new or existing systems to be upgraded or extended. Responsible for project activities required to scope, develop, procure, install, and qualify automation systems used in pharmaceutical manufacturing processes / utilities' systems Moderates and organizes multi-disciplinary teams and activities through project life cycle activities to deliver project scopes to meet global and local strategic requirements. Understanding of interfaces between the automation systems and process equipment / utilities systems and interfaces to IT systems / MES. Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval. Generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for senior site management and Global Steering Committees

Key Skills and Requirements:

Proven understanding of automation systems related to pharmaceutical business Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility. Understanding of GMP requirements related to automation systems, and related principles (data integrity, ERES, compliance to 21-part part 11, …) Ideally experience with Trackwise 5+ years practical and leadership experience in pharmaceutical industry including direct management experience in Manufacturing, Engineering or Execution Systems' function. Understanding of project management principles, project life-cycle phases and stage gate methodology. Proficiency in German and English. Strong organizational skills Excellent teamwork and communication skills.

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