Project Manager

Biogen is looking for an experienced Project Manager for our Project Engineering department at our Hillerod site.

Job Category

Engineering

Requisition Number

33960BR

Job Description

The Project Engineering department is managing the capital project portfolio (CapEx) for the site and we lead the CapEx projects through the entire live cycle from the early conceptual phases until handover. 

As a Project Manager in Project Engineering, you will lead the projects through all phases of the projects and be responsible for a safe project execution with no safety incidents, GMP incidents or other unintended interruptions of the daily operations.

In Project Engineering, you will be part of a team of six colleagues based in Hillerod. You will be managing a wide range of CapEx projects varying in size and complexity. Your specific responsibilities, will be control and management of scope, schedule and cost of capital projects. You will drive the project governance structure and manage the design, construction, safety and quality activities in the projects you lead.

In this position, you will also provide subject matter expertise in design reviews and technical investigations. You will participate in technology transfers of new products and processes. You will play an important role in equipment improvement and optimization projects and be a part of cross site standardization processes- and projects. 

Process engineering knowledge and process design experience from the pharmaceutical and/or biotech industry is an advantage for this position, as you should have the capability to provide engineering support for cell culture, purification, and pharmaceutical processing equipment and plant utilities. 

Primary Responsibilities:
• Project management of capital projects.
• Management of project specification activities: Definition of user requirements, generation and edit of P&IDs and other design specifications, specification and procurement of equipment and systems. 
• Management of project inspection and testing activities: Equipment inspections, factory acceptance testing (FAT), site acceptance testing (SAT), field verification and documentation review.
• Ensure effective commissioning and system start-up. Supervise internal and external resources during all phases of commissioning execution to facilitate efficient transition into validation.
• Provide technical support to Manufacturing, Manufacturing Engineering, Validation, and other site groups via system troubleshooting, investigations, studies, and scheduling support.

*LI-DEN2

Qualifications

You have a minimum of 5 years relevant project management- and process engineering experience from the pharmaceutical and/or biotech industry. 

Preferably you have experience within process and project engineering, civil work construction and label and packaging equipment. It is an advantage if you are knowledgeable about process systems, facilities, utilities, and production support equipment for manufacturing commercial-scale biopharmaceutical bulk drug substance.
You have a good understanding of business processes across the organization and insures that your projects are setup and organized to meet the specific need. 
You are a team player with focus on team performance and inclusion of the right skills and competencies. 
You possess good communication skills in Danish and English

Education

You have a Bachelor’s degree in Engineering, preferably within Chemical, Mechanical, or Process Engineering.

Please send your CV and application latest Sunday April 15th. For further information please feel free to contact Sr Recruiting Partner Eva Op De Beeck on phone +4525663058

Employment Category

Full-Time Regular

Experience Level

Associate


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