Process Engineer

Biogen in Hillerød is looking for a dedicated, result-oriented Process Engineer for the Purification team. The team is part of the Process Engineering group which is responsible for maintaining highly reliable and compliant process equipment and systems for Bulk Drug Substance manufacturing

Job Description

Your primary focus will be to provide engineering support and troubleshooting for all process equipment and technical operations within the Purification area. Additionally, you will take a leading role in optimization of the existing process equipment to continuously improve safety, robustness, operability and throughput. You will be also involved in projects related to the design and implementation of new process equipment. You also play an important role in transferring new manufacturing processes to the facility.
The tasks and responsibilities of the Process Engineer can be summarized as below:

• Troubleshoot and investigate process or equipment failures and implement changes to avoid future occurrences
• Ensure equipment compliance (Maintaining documentation)
• Provide supervision and take ownership of equipment changes and upgrades
• Assess equipment needs and generate equipment specifications for fabrication or purchase
• Help implement new manufacturing processes for new products or modifications to existing products
• Work cross-functionally with Manufacturing, Validation, Quality, Automation, Manufacturing Sciences, and Instrumentation & Controls, among others
• Be part of the team’s on-call support



The ideal candidate has a relevant degree in combination with 2-5 years’ experience in a pharmaceutical or biotech manufacturing environment. Preferably, the candidate has solid knowledge of processing of biological drugs. Alternatively, an in-depth understanding of industry scale processing plants in general would be relevant.
To achieve success you will need a systematic and analytical approach and be able to maintain the overview when working on several projects simultaneously.

Biogen has a growing pipeline of products, why it is important that you are adaptable and have a flexible attitude. You should furthermore have the ability to communicate constructively with colleagues at all levels in the organization. In addition, it is expected that you have:

• Knowledge of GMP and EMEA/FDA regulations (or experience working in a similar highly regulated environment)
•Excellent oral and written communications skills in English


BS/MS Degree in Engineering with related industry experience

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