Engineering Project Manager
On behalf of our client, an international biopharmaceutical company, Swisslinx is looking for a Engineering Project Manager. In this you will lead CAPEX projects in a GMP environment, in the field of Fill, Finish and Packaging from feasibility to planning, execution and
qualification/validation within the remit of the global engineering and project delivery department.
Contract type - 12 months
Start Date - ASAP
Location - Bern
Workload - 100%
Work type â?? hybrid or remote possible
Your mission:
â?¢ Support to local execution lead for improvement projects regarding Sterility Assurance, aligned with Local and Global stakeholders
â?¢ Leading of CAPEX projects in the field of Filling and Finish (Visual Inspection and Packaging)
â?¢ Responsible for project activities required to scope, develop, procure, construct and qualify new equipment and facilities required to meet facility production throughput demands
â?¢ Participates in multi-disciplinary Teams through project life cycle activities to deliver capacity expansion capabilities to meet global and local strategic requirements
â?¢ Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval
â?¢ Project Teams are responsible for completion of project life-cycle activities through turnover to routine commercial production
â?¢ Support for generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for senior site management and Global Steering Committees
Your background:
â?¢ Fluent German and English, written and spoken (MANDATORY)
â?¢ Proven knowledge regarding Sterility Assurance driven projects and the revised EU GMP Annex 1 "Manufacture of Sterile Medicinal Products"
â?¢ MS/MBA/BS/BA in Engineering, Business Administration or Life Sciences preferred or local equivalent
â?¢ 2+ years practical and leadership experience in pharmaceutical industry including direct management experience in Manufacturing, Engineering or Quality Assurance
â?¢ Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility
â?¢ Understanding of project management principles and project life-cycle phases. Knowledge of Validation, CMC and facility regulatory submission requirements
What's on offer
â?¢ An initially 12 month contract at an internationally-renowned biopharma company.
â?¢ A varied job in a dynamic but stable environment with the opportunity for professional development.
â?¢ A competitive salary.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: Write an email.
qualification/validation within the remit of the global engineering and project delivery department.
Contract type - 12 months
Start Date - ASAP
Location - Bern
Workload - 100%
Work type â?? hybrid or remote possible
Your mission:
â?¢ Support to local execution lead for improvement projects regarding Sterility Assurance, aligned with Local and Global stakeholders
â?¢ Leading of CAPEX projects in the field of Filling and Finish (Visual Inspection and Packaging)
â?¢ Responsible for project activities required to scope, develop, procure, construct and qualify new equipment and facilities required to meet facility production throughput demands
â?¢ Participates in multi-disciplinary Teams through project life cycle activities to deliver capacity expansion capabilities to meet global and local strategic requirements
â?¢ Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval
â?¢ Project Teams are responsible for completion of project life-cycle activities through turnover to routine commercial production
â?¢ Support for generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for senior site management and Global Steering Committees
Your background:
â?¢ Fluent German and English, written and spoken (MANDATORY)
â?¢ Proven knowledge regarding Sterility Assurance driven projects and the revised EU GMP Annex 1 "Manufacture of Sterile Medicinal Products"
â?¢ MS/MBA/BS/BA in Engineering, Business Administration or Life Sciences preferred or local equivalent
â?¢ 2+ years practical and leadership experience in pharmaceutical industry including direct management experience in Manufacturing, Engineering or Quality Assurance
â?¢ Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility
â?¢ Understanding of project management principles and project life-cycle phases. Knowledge of Validation, CMC and facility regulatory submission requirements
What's on offer
â?¢ An initially 12 month contract at an internationally-renowned biopharma company.
â?¢ A varied job in a dynamic but stable environment with the opportunity for professional development.
â?¢ A competitive salary.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: Write an email.
À propos de l'entreprise
