QA Manager in CMC QA
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Måløv
Are you interested in leading a team of dedicated and specialized QA Employees, making a significant impact in leadership? Are you motivated by challenging situations that demand high professional competency and leadership experience? If so, we have an opportunity for you. We are currently seeking a Manager to lead our CMC OP Dev CMO QA team (Chemistry, Manufacturing and Control, Oral Product Development, Contract Manufacturing Organizations) in Måløv. The position
Novo Nordisk is expanding within small molecules. In this role, you will lead a team of highly competent and experienced QA professionals who are focused on establishing our Quality Management System and overseeing drug product release for clinical trials from CMO’s. The team is slated to expand with several new QA’s the coming year. Reporting directly to the Director in CMC OP Dev QA & Analysis QA, you will be part of CMC OP Dev QA & Analysis QA management team, which includes the Director and three Managers. Your responsibilities will include:
• Ensuring the team possesses the necessary skills and competences, while fostering and maintaining close collaboration with stakeholders.
• Incorporating simplicity into processes and work methodologies, maintaining a continuous focus on simplicity within the department.
• Demonstrating visible leadership, emphasizing active listening and setting a clear direction for the team.
• Providing guidance, coaching, and support for the growth and development of team members.
You will get a broad range of exciting challenges with impact on the results for the SVP area feeding into your personal and professional development. Our working environment is flexible, dynamic, and informal with a strong culture of cross-functional collaboration. Qualifications
The most important asset that you can bring into this job is a well-developed understanding of leadership and quality and a natural urge to handle issues at the right level, make decisions and follow-up. To succeed in this role, you have:
• Master within pharmacy or biotechnology or similar.
• Experience from a pharmaceutical company.
• Experience with leadership and developing people.
• Written and verbal communication skills in English (Danish will be an advantage). As a person, you possess a proactive attitude, striving for higher performance and embracing challenges from peers and employees. It's crucial to maintain an excellent quality mindset, balancing compliance and product quality in decision-making, and remaining resolute when necessary to ensure quality and compliance. Your strong organizational skills yield results by inspiring employees to take pride in meeting their objectives. You are self-driven and capable of working independently, while recognizing the paramount importance of teamwork for success. It is essential that you excel in working with and developing people and the organization. About the department
You will become part of a department (CMC OP Dev QA & Analysis QA) consisting of three teams where we currently are 35 dedicated colleagues. You will be part of a strong culture, where we strive for high psychological safety, give regular feedback, and understand that the most important thing we have is our people. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release drug candidates for clinical trials. As part of Novo Nordisk Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients.
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 careers 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 50,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Director Casper Yding at +45 3079 7015.
Deadline
25 April 2024.
Please note that we will conduct interviews on an ongoing basis, so please submit your application 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.
Novo Nordisk is expanding within small molecules. In this role, you will lead a team of highly competent and experienced QA professionals who are focused on establishing our Quality Management System and overseeing drug product release for clinical trials from CMO’s. The team is slated to expand with several new QA’s the coming year. Reporting directly to the Director in CMC OP Dev QA & Analysis QA, you will be part of CMC OP Dev QA & Analysis QA management team, which includes the Director and three Managers. Your responsibilities will include:
• Ensuring the team possesses the necessary skills and competences, while fostering and maintaining close collaboration with stakeholders.
• Incorporating simplicity into processes and work methodologies, maintaining a continuous focus on simplicity within the department.
• Demonstrating visible leadership, emphasizing active listening and setting a clear direction for the team.
• Providing guidance, coaching, and support for the growth and development of team members.
You will get a broad range of exciting challenges with impact on the results for the SVP area feeding into your personal and professional development. Our working environment is flexible, dynamic, and informal with a strong culture of cross-functional collaboration. Qualifications
The most important asset that you can bring into this job is a well-developed understanding of leadership and quality and a natural urge to handle issues at the right level, make decisions and follow-up. To succeed in this role, you have:
• Master within pharmacy or biotechnology or similar.
• Experience from a pharmaceutical company.
• Experience with leadership and developing people.
• Written and verbal communication skills in English (Danish will be an advantage). As a person, you possess a proactive attitude, striving for higher performance and embracing challenges from peers and employees. It's crucial to maintain an excellent quality mindset, balancing compliance and product quality in decision-making, and remaining resolute when necessary to ensure quality and compliance. Your strong organizational skills yield results by inspiring employees to take pride in meeting their objectives. You are self-driven and capable of working independently, while recognizing the paramount importance of teamwork for success. It is essential that you excel in working with and developing people and the organization. About the department
You will become part of a department (CMC OP Dev QA & Analysis QA) consisting of three teams where we currently are 35 dedicated colleagues. You will be part of a strong culture, where we strive for high psychological safety, give regular feedback, and understand that the most important thing we have is our people. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release drug candidates for clinical trials. As part of Novo Nordisk Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients.
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 careers 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 50,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Director Casper Yding at +45 3079 7015.
Deadline
25 April 2024.
Please note that we will conduct interviews on an ongoing basis, so please submit your application 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 Måløv.
Jobbet er oprettet på vores service den 10.4.2024, 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
- Måløv
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