Experienced Professional for optimisation and validation
Are you motivated by optimisation and the prospect of working with introduction of new products and product transfers? Are you experienced working in a GMP regulated environment, and would you like to work with the newest equipment and technology in filling? Then we offer you a unique opportunity to apply and expand your skillset in our newly established filling facility
In this position, you will join the process support team and become part of our “back-office” support function. Your position will be focused around support to our two isolator filling lines including equipment and processes and you will be responsible for ensuring that we live up to regulatory standards and are ready for inspections from the authorities.
Specifically, your tasks will include creating and maintaining standards, validation and requalification, ensuring that all procedures are well in place before we start our actual production, and eventually release insulin products. In addition, you will work with optimisation of processes and procedures using LEAN as your primary methodology.
Throughout your work, you will have a broad range of stakeholders and a collaborate across different teams allowing you to build a broad network throughout the organisation. Our factory is dynamic, and two workdays will never be the same.
We imagine that you have an academic degree within the natural sciences, pharmacy or engineering. In addition, you have a minimum of 3 years of work experience in a regulated production environment, and a solid hands-on understanding of GMP requirements and LEAN methodologies. Experience with filling processes, isolator technology, or new product introduction would be considered an advantage. Professional proficiency in oral and written English is a prerequisite.
As a person, you have a strong quality mindset and thrive in a work environment that offers a high degree of variation, and many social interactions. Getting along with others, communicating effectively and collaborating across teams and functions come natural to you, and you always manage to stay solution oriented.
About the department
You will be part of Diabetes Finished Products (DFP), and more specifically you will be part of the department AP Filling and Inspection where 82 skilled and engaged colleagues would be welcoming you. The department located in Hillerød in a facility referred to as APX (Aseptic Production Expansion) – a state of the art filling facility which is just a few years old. The department is responsible for operations, maintenance, validation and qualification of our two new isolator filling lines.
We have been underway in an exciting project phase and are now performing the final process validations and qualifications before moving into production. We will be a launch site for all new products in Novo Nordisk, meaning that we will be tasked with the amazing challenge of being able to produce all the products in our diabetes portfolio.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
If you have questions about the position, please contact Associate Manager Steffen Elholm on phone +45 3079 4709
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
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