Process Engineer
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Kalundborg
Are you passionate about working in a production department that produces a highly regulated product to a changing market? Do you possess great IT skills? Do you have a high quality mindset and are driven by ensuring efficient processes? If yes, you might be our new colleague to join our production department in Biotech & Rare Diseases. Apply today! The Position At Biotech & Rare Disease Finished Products Kalundborg, we are looking for a new process engineer to support our team. You will be joining a team of 11 highly dedicated colleagues, whose main responsibility is ensuring the equipment on the filling line complies with GMP, and that it runs smoothly both mechanically and in terms of software. Your main job tasks include:
• Optimization of process.
• Support to process support for aseptic filling and process aids.
• Systematic problem solving in production.
• Document handling, this include; review, approval and elaboration of SOP, development and registration of documents.
• Collaboration across CVP (Change Verification Protocol) area – securing stakeholder management during optimization. You will be working in a busy, but social, young, and informal environment, where we emphasize collaboration, optimism, engagement, well-being, humour, commitment, and compliance.
We offer you an exciting job in an open and dynamic work environment with good opportunities for professional and personal development.
Qualifications To be considered for this position, we imagine that you have: • A degree in software engineering, computer science or similar, or a degree within natural science with coding knowledge. Newly graduates are welcome to apply.
• Great interest in working with- and develop skills in automation systems.
• Knowledge of validation.
• Knowledge of work in a project organisation.
• High verbal and written communication skills in English. As a person, you possess good analytical skills, you have a high-quality mindset, and meet your deadlines. You work well both individually, and as part of a team. With your structured approach to your tasks, you maintain an overview – and you adapt well to changes. About the Department Our team is part of the BRD Finished Products Kalundborg area that is part of our largest production complex in Novo Nordisk. Here we are app. 160 colleagues in the department who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We rely on our high-volume filling facility. Our complex processes require a high level of expertise, commitment, and engagement from our employees and include filling, product inspection, batch review and release. 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 in 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 are also stiving 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 If you have any questions regarding the position, please contact Louise Bruun Jørgensen at 30798788.
Deadline 20 August 2023, but applicants are reviewed on an ongoing basis. 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.
• Optimization of process.
• Support to process support for aseptic filling and process aids.
• Systematic problem solving in production.
• Document handling, this include; review, approval and elaboration of SOP, development and registration of documents.
• Collaboration across CVP (Change Verification Protocol) area – securing stakeholder management during optimization. You will be working in a busy, but social, young, and informal environment, where we emphasize collaboration, optimism, engagement, well-being, humour, commitment, and compliance.
We offer you an exciting job in an open and dynamic work environment with good opportunities for professional and personal development.
Qualifications To be considered for this position, we imagine that you have: • A degree in software engineering, computer science or similar, or a degree within natural science with coding knowledge. Newly graduates are welcome to apply.
• Great interest in working with- and develop skills in automation systems.
• Knowledge of validation.
• Knowledge of work in a project organisation.
• High verbal and written communication skills in English. As a person, you possess good analytical skills, you have a high-quality mindset, and meet your deadlines. You work well both individually, and as part of a team. With your structured approach to your tasks, you maintain an overview – and you adapt well to changes. About the Department Our team is part of the BRD Finished Products Kalundborg area that is part of our largest production complex in Novo Nordisk. Here we are app. 160 colleagues in the department who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We rely on our high-volume filling facility. Our complex processes require a high level of expertise, commitment, and engagement from our employees and include filling, product inspection, batch review and release. 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 in 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 are also stiving 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 If you have any questions regarding the position, please contact Louise Bruun Jørgensen at 30798788.
Deadline 20 August 2023, but applicants are reviewed on an ongoing basis. 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 Kalundborg.
Jobbet er oprettet på vores service den 2.8.2023, 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
- Kalundborg
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