Pilot Scientist for Purification
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Do you wish to make an impact on the products of the future? And do you thrive in a dynamic and scientific environment, where you are in the middle of R&D and production? We are looking for a motivated, skilled, and independent Pilot scientist for our Purification Pilot. Apply today! For an introduction to our area - CMC API Pilots - please visit our career page The position As Pilot Scientist you are responsible for driving production campaigns in the facility. That includes planning, dimensioning, and follow up on daily operation during the campaign as well as ensuring completion and final release. We are producing for clinical trials, and therefore GMP and documentation is a large part of our daily life. The team consists of technicians and scientists and are a very social, positive and including team with can-do attitude and lots of humour.
In you job you will collaborate with a wide range of stakeholders including process development laboratories, support functions, QA and possibly CMO.
You will have great opportunities to be involved in interdisciplinary projects, tasks and problem-solving where you can put your scientific knowledge and process understanding into play. Qualifications To be successful in this role, we imagine that you have an engineering degree or a master’s degree within chemistry, pharmacy, or a similar field. Preferably, you also have experience or knowledge within one or more of the following: Protein purification in pilot or production scale
Separation techniques such as filtration, chromatography, and precipitation
Organic chemistry and chemical modifications
Experience from a GMP regulated production is an advantage.
We welcome applications both from senior profiles with strong scientific expertise, and from more junior profiles within the field, who are ambitious about developing in the role. As a person, you work independently, can handle a complex workday, and enjoy a close and friendly collaboration with your team and department. You are responsible, flexible, and have the courage and drive to engage in new assignments and stick to them until the job is finished. It is important that you are a good communicator, since you are in daily contact with other scientists, technicians, production employees, project managers, analytical laboratories, and others. A positive mindset will suit our working environment where a good laugh is appreciated even when things are getting hectic. About the Department As part of PSQIT organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical tri-als and have a strong culture with a “can do” mind-set. CMC API Pilots manufacture and control new drug substance candidates for the develop-ment portfolio at . Purification Pilot Plants consists of 5 teams, and we are approximately 70 employees. Our task is to scale up processes, purify and dry proteins for toxicological and clinical studies of the portfolio. The facility is located in Bagsværd Our mission is to develop robust and reliable API-processes for clinical trials to support our portfolio of drug candidates in . We have focus on innovation, quality, and efficiency to improve the life of the patients. Working at At , 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. Contact For further information, please contact Charlotte Hother le Fevre, Senior Director, Purification Pilot Plants at +. Deadline 3 November 2024. Applications will be reviewed on on-going basis, and 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 lines about your motivation in your resume or CV. In addition, please avoid the use of photos in your CV. This provides a better and more fair process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At 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.
In you job you will collaborate with a wide range of stakeholders including process development laboratories, support functions, QA and possibly CMO.
You will have great opportunities to be involved in interdisciplinary projects, tasks and problem-solving where you can put your scientific knowledge and process understanding into play. Qualifications To be successful in this role, we imagine that you have an engineering degree or a master’s degree within chemistry, pharmacy, or a similar field. Preferably, you also have experience or knowledge within one or more of the following:
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 18.10.2024, 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.
- Øvrige
- Bagsværd
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