Quality Coordinator
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Måløv
Do you have passion for quality, and are you motivated by setting compliance standards and ensuring that we continuously simplify and improve our processes and ways of working? Do you get empowered from working with a wide range of highly qualified colleagues? Then you could be the new Quality Coordinatorfor the department CMC Analytical Support in Måløv, Denmark. As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (CMC) Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture, and distribute drug candidates for non-clinical and clinical trials and represent a strong culture with a “can do” mind-set.
We are looking for a professional with a background in the pharma industry who enjoy interacting with people and as the ability to communicate with colleagues at all levels of the organisation. We are searching for an individual who has the ability to spot opportunities for process simplicity and improvements across our department in order to securing compliance. The position You will work closely together with the department’s leadership and management team and refer to the department manager. You will be an active member of our Quality Management System/QMS team across the CVP area and join selected cross functional process groups setting direction for quality management across Novo Nordisk. You will be responsible for supporting management and colleagues in maintaining our quality level and in seeking new ways of working. You will Ensure high-level GMP overview, and report quality trends to management Lead and coordinate critical quality issues and compliance activities in department and across our CVP area Drive preparation for and follow-up on authority inspections and internal audits together with our CVP area QMS team Work in Quality Management Systems, responsible for Q-Plan establishment incl. follow-up and Training developer responsible Supporting daily operation with quality and ensure sufficient level of GMP and GSP processes on shopfloor
Qualifications You have an MSc within pharmacy, engineering or similar 3 years’ experience from the pharmaceutical industry, preferably experience from GMP regulated areas You think and act with a broad and holistic perspective, seeing the big picture without losing sight of details The position requires a quality mindset, the ability to work independently, and a wish to act as a role model in setting the direction in Quality and Compliance incl. Training
As a person you are positive, analytical, action and solution orientated, and you work systematically, and proactively. Additionally, you are a team player who enjoys driving own area of responsibility. You are dedicated towards meeting our common goals and you are not afraid to lead the way for colleagues. You push your agenda forward in a dynamic environment where projects and processes vary. You take initiatives independently and ensure commitment from your stakeholders. You have focus on change management when introducing your ideas and the ability to set direction when it is needed. About the department
The department, CMC Analytical Support, is organised into four highly skilled analytical teams with a total of 65 employees. The department is responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substance, drug product and side chains as well as for raw materials, excipients, and various process related residues and leachables. Furthermore, we are responsible for small molecule, peptide and protein characterisation including particle characterisation and stability studies. Providing analytical support to all parts of Novo Nordisk, the department acts as a link between the research unit and the production, spanning from early development to phase 3 clinical trials and registration. Together we represent many years of scientific experience enabling us to innovate and solve exciting and challenging tasks. Working at Novo Nordisk At Novo Nordisk, 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. Contact For further information, please contact Ulla Kvottrup at +45 3079 4949 Deadline Job interviews will be held continuously, so please do not hesitate to apply. April 10th, 2023 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.
We are looking for a professional with a background in the pharma industry who enjoy interacting with people and as the ability to communicate with colleagues at all levels of the organisation. We are searching for an individual who has the ability to spot opportunities for process simplicity and improvements across our department in order to securing compliance. The position You will work closely together with the department’s leadership and management team and refer to the department manager. You will be an active member of our Quality Management System/QMS team across the CVP area and join selected cross functional process groups setting direction for quality management across Novo Nordisk. You will be responsible for supporting management and colleagues in maintaining our quality level and in seeking new ways of working. You will
Qualifications
The department, CMC Analytical Support, is organised into four highly skilled analytical teams with a total of 65 employees. The department is responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substance, drug product and side chains as well as for raw materials, excipients, and various process related residues and leachables. Furthermore, we are responsible for small molecule, peptide and protein characterisation including particle characterisation and stability studies. Providing analytical support to all parts of Novo Nordisk, the department acts as a link between the research unit and the production, spanning from early development to phase 3 clinical trials and registration. Together we represent many years of scientific experience enabling us to innovate and solve exciting and challenging tasks. Working at Novo Nordisk At Novo Nordisk, 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. Contact For further information, please contact Ulla Kvottrup at +45 3079 4949 Deadline Job interviews will be held continuously, so please do not hesitate to apply. April 10th, 2023 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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 3.3.2023, 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.
- Forretningsudvikler
- Måløv
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