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Quality Control Process Scientist
2 months ago
Are you passionate about enhancing the lives of individuals with chronic conditions? Do you have a strong foundation in High-Performance Liquid Chromatography (HPLC) and other analytical techniques within a GMP-compliant framework? If you are eager to embrace new challenges and take on increased responsibilities, this role may be the perfect fit for you.
Position Overview
As a Process Scientist in the Quality Control (QC) laboratory, you will play a crucial role in ensuring the quality of our pharmaceutical products. You will collaborate with a dedicated team of 20 professionals, including fellow scientists and laboratory technicians, to perform HPLC analyses and support the production of Active Pharmaceutical Ingredients (API).
Your responsibilities will include:
- Coordinating tasks across various departments to enhance workflow efficiency.
- Providing guidance and support to laboratory technicians.
- Streamlining processes, implementing improvements, and addressing any deviations.
- Engaging in Lean methodologies and data analysis to optimize operations.
This is a temporary position for a duration of 1.5 years.
Required Qualifications
We are looking for candidates who possess:
- A minimum of a master's degree in natural sciences, engineering, pharmacology, or a related field.
- Experience in GMP environments and familiarity with cLEAN principles.
- Proficiency in HPLC analysis within the pharmaceutical sector or other GMP-regulated settings, along with QC compliance experience, which is advantageous.
- Excellent command of written and spoken English and Danish.
Personal Attributes
The ideal candidate will demonstrate a strong sense of curiosity, a good sense of humor, and a positive attitude. You should be capable of working independently in a structured manner while also being an effective team player, fostering collaboration across departments.
Success in this role requires the ability to thrive in a dynamic environment, proactively taking on responsibilities and identifying opportunities for improvement. Strong organizational skills and the ability to manage multiple priorities effectively are essential.
About Our Department
The Active Pharmaceutical Ingredients (API) division, located in Kalundborg, is dedicated to producing insulin and GLP-1 to support individuals with chronic conditions such as diabetes and obesity. Our department is involved in numerous innovative projects, ranging from establishing new processes to optimizing existing ones.
The Insulin Manufacturing 1 facility in Kalundborg is recognized as the largest insulin production site globally, where we manufacture the active ingredients for many of Novo Nordisk's products, including our new oral medication. The QC department within IM1 comprises five teams, totaling approximately 60 colleagues, all committed to fostering a safe and engaging work environment that prioritizes well-being and collaboration.
