Operations Supporter
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Søborg
Are you thriving in driving process improvements? Do you think outside the box for the best solution? Are you taking pride in supporting continuous production and delivery of products to patients? If so, apply today and join our newly stablished team as Operations Supporter!
The Position As Operations Supporter, you will collaborate with Operations Managers, QA professionals, Specialists, and other departments to provide support and implement improvements. The role takes place in a dynamic, fast-paced environment. Global Contract Manufacturing department is physically located in Søborg, Denmark. Our Contract Manufacturing Organizations are located around the world; hence minor travel activity might be expected. Your focus will be on:
• assisting the entire Operations department with handling of deviations, Change Control Requests, handling of customer complaints, writing, maintaining, and updating procedures (SOP)
• supporting the daily operations in collaboration with Operations Managers, specialists, and QA professionals
• often interacting with Contract Manufacturing Organisations (CMOs) to learn their processes and to create a common understanding between their and our Quality Management systems (QMS)
• influencing the daily work through both team-based tasks and independent work Qualifications
The qualifications we value include:
• a bachelor’s or master’s degree in engineering, chemistry, or natural science with experience in pharmaceutical production; minimum of 2 years of relevant experience if a candidate has no pharmaceutical background
• recently graduated pharmacists are welcome to apply, and we will provide all necessary training
• good understanding of GMP environment and proficiency in authoring documents
• previous training or experience in LIMS systems, deviations and change control handling is a plus
• fluency in written and spoken English As a person, you have a high-quality mindset and take pride in delivering on your deadlines. You work well independently, although are also be motivated to cooperate with colleagues and stakeholder across the functions and departments. Personal drive, positive energy, good communication skills and the ability to build relationships are keys to thrive in this role. With analytical problem-solving skills, you take on any challenge with ease. About the department GCM is part of Novo Nordisk’s Product Supply organization and is responsible for Novo Nordisk contract and license manufacturing of intermediates, drug substances, semi-finished and finished drug products to global markets. The primary role of GCM Operations is to monitor, control and develop the production handled by CMO’s and to ensure delivery of products to our respective customers. We are responsible for all operations towards our CMO's and sourcing of products into Novo Nordisk according to the demand from our production sites and customers worldwide. We offer you an exciting job in an international environment with the possibility to play an important role in Novo Nordisk contract manufacturing organisation together with our Operation Managers, Quality Assurance, specialists, CMOs), and with a broad network across Novo Nordisk. You will join an experienced, diverse, talented, and supportive team where we have an informal and direct tone and where we value each other’s differences. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact For further information, please contact Zohra Shahabi on +45-30775903 or [email protected]. Deadline 03 December 2023. Please note that applications will be reviewed continuously. 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 written in English. 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.
The Position As Operations Supporter, you will collaborate with Operations Managers, QA professionals, Specialists, and other departments to provide support and implement improvements. The role takes place in a dynamic, fast-paced environment. Global Contract Manufacturing department is physically located in Søborg, Denmark. Our Contract Manufacturing Organizations are located around the world; hence minor travel activity might be expected. Your focus will be on:
• assisting the entire Operations department with handling of deviations, Change Control Requests, handling of customer complaints, writing, maintaining, and updating procedures (SOP)
• supporting the daily operations in collaboration with Operations Managers, specialists, and QA professionals
• often interacting with Contract Manufacturing Organisations (CMOs) to learn their processes and to create a common understanding between their and our Quality Management systems (QMS)
• influencing the daily work through both team-based tasks and independent work Qualifications
The qualifications we value include:
• a bachelor’s or master’s degree in engineering, chemistry, or natural science with experience in pharmaceutical production; minimum of 2 years of relevant experience if a candidate has no pharmaceutical background
• recently graduated pharmacists are welcome to apply, and we will provide all necessary training
• good understanding of GMP environment and proficiency in authoring documents
• previous training or experience in LIMS systems, deviations and change control handling is a plus
• fluency in written and spoken English As a person, you have a high-quality mindset and take pride in delivering on your deadlines. You work well independently, although are also be motivated to cooperate with colleagues and stakeholder across the functions and departments. Personal drive, positive energy, good communication skills and the ability to build relationships are keys to thrive in this role. With analytical problem-solving skills, you take on any challenge with ease. About the department GCM is part of Novo Nordisk’s Product Supply organization and is responsible for Novo Nordisk contract and license manufacturing of intermediates, drug substances, semi-finished and finished drug products to global markets. The primary role of GCM Operations is to monitor, control and develop the production handled by CMO’s and to ensure delivery of products to our respective customers. We are responsible for all operations towards our CMO's and sourcing of products into Novo Nordisk according to the demand from our production sites and customers worldwide. We offer you an exciting job in an international environment with the possibility to play an important role in Novo Nordisk contract manufacturing organisation together with our Operation Managers, Quality Assurance, specialists, CMOs), and with a broad network across Novo Nordisk. You will join an experienced, diverse, talented, and supportive team where we have an informal and direct tone and where we value each other’s differences. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact For further information, please contact Zohra Shahabi on +45-30775903 or [email protected]. Deadline 03 December 2023. Please note that applications will be reviewed continuously. 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 written in English. 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 Søborg.
Jobbet er oprettet på vores service den 9.11.2023, 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
- Søborg
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