Maintenance Support
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Kalundborg
Are your analytical skills strong and do you enjoy a hands-on approach to your field? Can you add to the success story of Novo Nordisk and ensure the highest level of quality in the production of life-changing medicine to biopharmaceutical products worldwide? Would you like a range of opportunities for personal and professional development? Then you might be our new Maintenance supporter of our dedicated support team within Aseptic Production (AP). The position Your primary goal is to ensure that the production consistently delivers a high-quality product in compliance with internal quality requirements and GMP. Our team supports the production on shop floor, and our field of responsibility for the filling processes covers the validation of the lines, the operational procedures to operate them, the expertise in the products and the continuous improvement of the filling lines. The main role is Guarantee the Validation Status in our Equipment and Process, Equipment qualification and be responsible for managing/participating in systematic problem-solving (SPS) related to DV´s in own team. As part of your responsibilities, you will: Support development of competences, work in compliance with some SOP, build maintenance strategy, plans and frequency, Maintenance Work Description [MWD], Change Control for related equipment, ensure machine safety [CE marking]. Support the future maintenance strategy and operational platform [LCM], support end user training setup for operators and maintenance teams, to ensure faster support for production units, optimization of equipment according to future strategy Handle a range of stakeholders with diverse and possibly conflicting needs and concerns in a way that ensures the optimal collaboration across professional and cultural distances – and has the continuation of a stabile production chain as a result. Take part in SPS processes, development and optimization projects and develop a broad understanding of a complex value chain, when you provide our collective expertise across a truly global organization. When you are ready, you will support the development of competencies in our production team and participate in audits and inspections. Whenever something is out of the ordinary and/or something needs changing, we help make everything run again as quickly as possible and ensure that the right validation procedures are in place, challenging external vendors on specifications and technical issues when necessary. Qualifications To succeed in this role, we expect you to have: An academic degree in biochemistry, bioengineering, automation engineering, or similar. Preferably + 2 years of experience from the pharmaceutical industry after graduating. Knowledge about aseptic production and behavior as well as current knowledge in process automation in biotech is highly advantageous. Great interest in working with GMP and LEAN. Fluency in English. The ability to communicate in Danish is a benefit. As a person, you are open and honest, independent as well as team player and flexible to changes. You have good communication skills and the ability to efficiently work with concurrent tasks. Being proactive, responsible and energetic is a key to succeed in this position. In return, you will find opportunities for personal and professional development here that will be hard to come by elsewhere. About the department In Biopharm, we produce a range of products that help people live with chronical diseases like haemophilia and hormonal imbalances. In our new filling and inspection facility, we will be filling the Active Pharmaceutical Ingredients (API) onto vials and dosage systems. In other words, we make the products ready for packing and distribution with all the processes that are involved in this – from various visual inspections over actual filling procedures to all the documentation that is necessary for us to comply with regulatory and quality standards. Our filling and inspection facility is ready to enter the next phase, and now we are looking into a period of production ramp up, which in turn initiates many process optimization projects. You will be part of a support team of dedicated and talented academics and technicians. Our tone is relaxed, and if you enjoy sharing your knowledge and learning from others, you will enjoy working here. The facility is located at our site in Kalundborg with approximately 350 employees. Working at BRD FP Novo Nordisk Finished Products site Kalundborg is part of Biotech & Rare Disease. At our site in Kalundborg, we are more than 650 colleagues responsible for transforming the API (Active Pharmaceutical Ingredient) into the finished medicine for people living with serious chronic diseases. We work with advanced processes such as formulation, filling, freeze-drying in a sterile environment. We bring value to our patients by delivering high-quality products in accordance with Good Manufacturing Process (GMP) in a timely and cost-effective manner as we constantly optimise our processes and invest in the latest technology. Contact For further information about the position, please feel free to call Julio Santiago , 34 48 06 96.
Deadline 22 October 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.
Deadline 22 October 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 Kalundborg.
Jobbet er oprettet på vores service den 3.10.2023, 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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