Environmental Monitoring Project Chemist
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Gentofte
Are you driven by the opportunity of gaining a professional development by being responsible for tasks where the knowledge and standards will elevate as the projects progresses? Do you want to make an impact and be the one responsible for the microbiological environment in our new isolators? Then it is you, we are looking for in our project position! The position
Environmental Monitoring (EM) is one of the most important controls in clean areas and provides meaningful information on the quality of the environment for aseptic processing. As Environmental Monitoring Project Chemist, you will be a part of the project process support team and responsible for: Securing, defining, and establishing microbiological monitoring inside our isolator filling lines and being our microbiological monitoring go to person. Working with defining the microbiological sample locations based on rationales for worst-case locations based on your knowledge, experience and data during test on the line. Writing rationales and other necessary documentation for securing implementation of the environmental monitoring before and during the production of our aseptic products according to current requirements and GMP. EM performance verification of grade A isolators performed to document that the environment is in control with respect to monitoring of airborne microorganisms, non-viable particles in air and microorganisms on surfaces. Even though you are responsible for a specific area, you will be collaborating closely with your colleagues in solving your tasks and together we will find the right solution. If you are self-driven, but collaborative and solution-oriented with a passion of driving and executing complex projects you can be an essential element in this team, contributing to the development of projects where the environmental stabilities are critical components. Qualifications
To succeed in this role, you have: A Master’s degree within natural science, which could be Pharmacy, Microbiology or other relevant areas Experience in working with microbiology in an aseptic pharmaceutical production area +2 years of pharma experience will be advantageous. Experience in working in a highly regulated environment under GMP (good manufacturing practice) Full professional proficiency in English On a personal level, you are proactive and have a strong quality mindset whilst keeping a structured, systematic and positive approach to problem solving when it comes to solving your tasks. Furthermore, you are a team player and are curious to understand and interact with your colleagues. About the department
Our team is part of the BRD Finished Products Gentofte and Vaarloese area that is the production site situated close to Copenhagen. Here we are app. 620 colleagues who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We are producing at full speed on existing lines while building and ramping up new state of the art facilities. Our complex processes require a high level of expertise, commitment, and engagement from our employees and include formulation, filling, freeze-drying, product inspection, assembly and pack. We bring value to patients by delivering high-quality Good Manufacturing Process (GMP) compliant products in a timely and cost-efficient manner. We drive change by working actively with LEAN and always looking for improvements within our processes, but also in the way we work together to make our products reach as many patients as possible. Working at BRD, Novo Nordisk
Biotech & Rare Disease (BRD) is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2650 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we also strive to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career? Contact
For further information, please contact project chemist Katrine Johansen Nielsen at +45 3079 1266 or Associate Manager, Kim Bech Poulsen at +45 3079 0613. Deadline
26 February 2023. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. 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.
Environmental Monitoring (EM) is one of the most important controls in clean areas and provides meaningful information on the quality of the environment for aseptic processing. As Environmental Monitoring Project Chemist, you will be a part of the project process support team and responsible for:
To succeed in this role, you have:
Our team is part of the BRD Finished Products Gentofte and Vaarloese area that is the production site situated close to Copenhagen. Here we are app. 620 colleagues who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We are producing at full speed on existing lines while building and ramping up new state of the art facilities. Our complex processes require a high level of expertise, commitment, and engagement from our employees and include formulation, filling, freeze-drying, product inspection, assembly and pack. We bring value to patients by delivering high-quality Good Manufacturing Process (GMP) compliant products in a timely and cost-efficient manner. We drive change by working actively with LEAN and always looking for improvements within our processes, but also in the way we work together to make our products reach as many patients as possible. Working at BRD, Novo Nordisk
Biotech & Rare Disease (BRD) is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2650 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we also strive to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career? Contact
For further information, please contact project chemist Katrine Johansen Nielsen at +45 3079 1266 or Associate Manager, Kim Bech Poulsen at +45 3079 0613. Deadline
26 February 2023. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 20.12.2022, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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