Do you excel in a dynamic and fast-paced setting where teamwork is essential for success? Do you thrive on mentoring peers and setting direction? Are you driven and enthusiastic senior professional, who is ready to join our Recovery and Purification Process team? If you are ready to make a meaningful impact on the lives of our patients, then apply today and embark on a life-changing career!
The Position
As a member of the Recovery and Purification Process team, you will work alongside 13 highly skilled and dedicated colleagues. Your primary role as a Senior Process Supporter will involve providing assistance with production-related tasks, including ensuring compliance with current standards and regulations, managing change requests, addressing complex deviations, and overseeing qualification and validation activities.
In addition, you will collaborate with stakeholders to optimize downstream processes. Key responsibilities include:
- Troubleshooting and problem-solving using methodologies such as A3 or similar.
- Coordinating activities with internal and external stakeholders.
- Leading improvement initiatives to ensure processes are smart, simple, and efficient.
Your specific tasks will vary based on your experience and qualifications.
Qualifications
To succeed in this position, you have:
- A relevant educational background in natural sciences, chemistry, or a related field.
- 5+ years of experience in the production and/or development of pharmaceutical products.
- Experience with GMP and LEAN methodologies.
- Fluency in Danish and English, both written and spoken.
As an individual, you bring a structured and proactive approach to work, with an unwavering commitment to quality. You excel at prioritizing and managing tasks effectively, ensuring deadlines are met without compromising quality.
You thrive in fast-paced environments with frequently changing priorities, maintaining composure and making sound decisions under pressure. Your ability to stay focused and perform in challenging situations is a valuable asset.
About the Department
You will join a dynamic business area that produces Active Pharmaceutical Ingredients (API) for patients worldwide. PS API FVII, also known as ED2, consists of two departments: Production and Support. We operate as one cohesive unit, collaborating as a unified team to produce Factor VII API for patients with haemophilia and post-surgical bleeding.
This position is within the Support department, where you will work alongside approximately 75 colleagues. As part of Novo Nordisk PS API, you will contribute to one of the world's largest and most successful pharmaceutical companies. We are always seeking talented individuals eager to grow and develop with us.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change – we drive it. As a dynamic company in an ever-evolving industry, we know that what brought us success today may not ensure success tomorrow.
We embrace experimentation and strive for excellence without fixating on perfection. We seize opportunities to develop and improve, taking bold steps to move the needle on patient care. From research and development to manufacturing, marketing, and sales, we’re united in our mission to make a difference in the lives of patients.
Contact
For further information, please contact Mia Sandø Søgaard, +45-34482787 at [email protected]
Deadline
January, 12th.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
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