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UDLØBET

Novo Nordisk A/S - A1p

Operational Responsible Enviromental Monitoring & Cleaning

Fuldtid

Permanent

ID: 2248338
|
Indrykket for 309 dage siden

Are you motivated by working in a changing environment? Would you like to be involved in a new capacity expansion project, in which you can influence and impact future Aseptic Production (AP) production facilities? If yes, we offer a great opportunity to become part of a team, where we turn ideas into actions. Apply today, and become our new Operational Responsible for Environmental Monitoring and Cleaning. 

The Position


In Biotech & Rare Diseases (BRD) expansion project in Måløv, we are planning to expand our production facilities. The aim of this new expansion project is to build a completely new manufacturing facility, including the implementation of isolator and other advanced technologies, with which Novo Nordisk has limited experience. This new facility aims to innovate our processes and to broaden our perspective, which is why this position requires a candidate with a good innovative mindset.
 

As our Operational Responsible for Environmental Monitoring and Cleaning, your main area of responsibility is getting processes and procedures ready for production.
 

Therefore, your main tasks will be:
• Responsible for all Environmental Monitoring & Cleaning activities.
• Project management and execution, including integration and cooperation with the program mirror organisation.
• Ensure that Systematic Problem Solving (SPS) and process confirmation are carried out in a structured way, and implementation of LEAN methodologies in the work carried out. 
• Responsible for Quality and Compliance, ensuring that internal and internal quality demands comply to Current Good Manufacturing Practice (CGMP). 


Though the project is located in Målev, interaction with the AP Expansion project on other sites is needed, and some travel or online-activity across the world, and time zones must be expected.
 

Qualifications

To be considered for this position you have:
• An academic degree (BSc., MSc. or PhD.)
• Solid understanding of Current Good Manufacturing Practice (GMP)
• Preferably 5 years of project management experience, and/or Environmental Monitoring. 
• Solid network within Product Supply (PS) and related areas within Novo Nordisk, or a lot of experience within the pharmaceutical industry. 
• High verbal and written communication skills in English, plus good presentation skills.

As a person, you have good cooperation and communications skills, and you are able to engage and coach own subordinates and other project team members. You are comfortable with working in an environment in constant change, with high complexity, and you are able to optimize, create and implement new working practices. You are result-oriented with a “can-do” attitude, being structured and organized with strong focus on high quality. 

About the Department

Our team is part of the Biotech & Rare Disease (BRD) Manufacturing Development & Quality Control area that has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 500 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio.
 
Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible.

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