QA Director in Active Pharmaceutical Ingredient
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Kalundborg
Would you like to join us in the early stage of our journey and make your mark on a QA department for our new Purification Plant? Are you eager to take part in establishing a factory that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing? If yes, then join us in shaping the future of our growing Purification Plant's QA department! Read more below and apply for a life-changing career! The position
You will play a crucial role in spearheading, developing, and shaping the new QA Purification Plant V (PPV) department's approach to quality assurance. This involves actively promoting and supporting a quality culture in collaboration with stakeholders at the Purification Plant. The goal is to ensure that products and processes adhere to both external and internal GMP requirements. In this role, you can also expect the following:
• Leading and building up a department of highly trained and experienced QA professionals and specialists
• Building and maintaining close collaboration with the production unit and other stakeholders across Novo Nordisk
• Ensuring that we as a company can deliver high quality products at competitive cost
• Driving prioritisation, strategies and setting direction for quality and compliance across sites
You will be the QA partner for the PPV area which includes being a member of the PPV management group assuring the unit and stakeholder areas have the relevant systems and procedures in place for securing compliance with relevant laws and guidelines. In your role, you will refer directly to the Corporate Vice President of API QA.
Qualifications
We are looking for an experienced manager, able to lead through other leaders as well as coaching and motivating your own associate managers and specialists to deliver their best. To succeed in this role, you have:
• A Master's degree in pharmacy, engineering, or a related field
• Substantial experience related to quality assurance in a pharmaceutical production
• Strong understanding of both the quality business and the production business with a strategic ability to balance quality, delivery and cost
• Demonstrated experience in establishing new departments or organizations
• Fluency in English Being proficient in Danish or showing a willingness to learn the language would be advantageous. As a person, you possess a quality-oriented mindset and adept stakeholder management skills. While fostering a results-driven environment, you ensure quality and compliance are upheld to safeguard patients. Your organizational prowess and effective communication are key assets for success in this role. About the department
You will be part of the PPV project to establish a super-sized purification facility for manufacturing of biological APIs in Kalundborg. We are expanding to increase production of Novo Nordisk’s current and future oral and injectable products by establishing a new and ground-breaking biotech facilities in Kalundborg. We embrace new technologies and we’re building a purification factory with a strong focus on digitalization, automation, and robotics. You will be heading up a department where behavioural targets are driving our culture and where setting direction for quality is driven through quality oversight and our ability to support and drive improvements. Working at Novo Nordisk
At Novo Nordisk, we do not wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we are all working to make a difference for millions of patients living with chronic diseases. Contact
For further information, please contact CVP, Camilla Kornbeck on +45 3075 1270. Deadline
07 January 2024. Please be advised that interviews will be conducted on an ongoing basis, so we encourage you 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.
You will play a crucial role in spearheading, developing, and shaping the new QA Purification Plant V (PPV) department's approach to quality assurance. This involves actively promoting and supporting a quality culture in collaboration with stakeholders at the Purification Plant. The goal is to ensure that products and processes adhere to both external and internal GMP requirements. In this role, you can also expect the following:
• Leading and building up a department of highly trained and experienced QA professionals and specialists
• Building and maintaining close collaboration with the production unit and other stakeholders across Novo Nordisk
• Ensuring that we as a company can deliver high quality products at competitive cost
• Driving prioritisation, strategies and setting direction for quality and compliance across sites
You will be the QA partner for the PPV area which includes being a member of the PPV management group assuring the unit and stakeholder areas have the relevant systems and procedures in place for securing compliance with relevant laws and guidelines. In your role, you will refer directly to the Corporate Vice President of API QA.
Qualifications
We are looking for an experienced manager, able to lead through other leaders as well as coaching and motivating your own associate managers and specialists to deliver their best. To succeed in this role, you have:
• A Master's degree in pharmacy, engineering, or a related field
• Substantial experience related to quality assurance in a pharmaceutical production
• Strong understanding of both the quality business and the production business with a strategic ability to balance quality, delivery and cost
• Demonstrated experience in establishing new departments or organizations
• Fluency in English Being proficient in Danish or showing a willingness to learn the language would be advantageous. As a person, you possess a quality-oriented mindset and adept stakeholder management skills. While fostering a results-driven environment, you ensure quality and compliance are upheld to safeguard patients. Your organizational prowess and effective communication are key assets for success in this role. About the department
You will be part of the PPV project to establish a super-sized purification facility for manufacturing of biological APIs in Kalundborg. We are expanding to increase production of Novo Nordisk’s current and future oral and injectable products by establishing a new and ground-breaking biotech facilities in Kalundborg. We embrace new technologies and we’re building a purification factory with a strong focus on digitalization, automation, and robotics. You will be heading up a department where behavioural targets are driving our culture and where setting direction for quality is driven through quality oversight and our ability to support and drive improvements. Working at Novo Nordisk
At Novo Nordisk, we do not wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we are all working to make a difference for millions of patients living with chronic diseases. Contact
For further information, please contact CVP, Camilla Kornbeck on +45 3075 1270. Deadline
07 January 2024. Please be advised that interviews will be conducted on an ongoing basis, so we encourage you 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 11.12.2023, 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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