Audits and Inspections Coordinator
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Kalundborg
Are you passionate about ensuring compliance and quality standards? Do you have experience in coordinating audits and inspections? We are looking for a skilled Audit and Inspections Coordinator to join our API Quality Assurance Operational and Business Support team at Novo Nordisk. If you are detail-oriented, knowledgeable about regulatory requirements, and have a strong background in GMP, then read on and apply today for a life-changing career.
The position
In this role, you will be a part of a team that has responsibility of coordinating audits and inspections and follow up on findings afterwards, where you will utilise your in-depth knowledge of compliance, requirements, and expectations from authorities to ensure the right level of compliance in the supply of active pharmaceutical ingredients. You will also respond to complex compliance questions and be responsible for coordinating, planning, and follow up on inspections and audits.
As an Audit and Inspections Coordinator, you will have the following responsibilities: Coordinate and contribute to planning and conducting audits and inspections (on-site, remote and paper-based), as well as providing answers to audit findings and inspection observations and a number of other requests from authorities. Being proactive in identifying needs for upcoming qualification audits in PS API. Help driving the cross-functional support group for audits and inspections in PS API. Contribute to coaching and sparring of employees to ensure a strong understanding of compliance with GMP requirements. Act as a sparring partner for PS API and PS API Quality Assurance regarding GMP. Moreover, you will be a specialist in your own area of expertise and act as a mentor for upcoming specialists or those needing guidance. Qualifications
To succeed in this role, you should have the following qualifications: A master’s degree in pharmacy, science, engineering, or similar Several years of experience working with compliance Several years of experience in the pharmaceutical industry, API, quality control (QC), and/or quality assurance Strong GMP knowledge, ability to follow current GMP development and relevant literature, as well as extensive knowledge and experience in quality assurance work Good stakeholder management skills Strong communication skills Fluency in English, both written and verbal As a person, you are good at acquiring new knowledge and have a desire to teach and disseminate knowledge. It is expected that you have strong business acumen.
Furthermore, you have excellent communication skills with the ability to collaborate, both with internal and external stakeholders.
About the department
You will join the business area of API Quality Assurance Operational and Business Support, which is a part of API Quality. Within this area, you will be a part of the department that drives projects, strategy, audits, and inspections, as well as IT, digitalisation, QA for QC & Manufacturing Development and much more. Our purpose is to set direction within our area of expertise and enable API Quality Assurance to meet our goals.
As a group, we get energy from solving problems, seeing opportunities, and driving impactful change. We focus on development while having fun at the same time; we are maintaining a social work environment with a high level of engagement. Our ambition is to provide world-class support to our key stakeholders, and we take pride in delivering on our commitments. 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 Amalie Nytoft Stjerneby on +45-30775168.
Deadline
28 April 2024
We will be reviewing the applications on an ongoing basis, and we therefore 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 your motivation to apply in your CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to 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
In this role, you will be a part of a team that has responsibility of coordinating audits and inspections and follow up on findings afterwards, where you will utilise your in-depth knowledge of compliance, requirements, and expectations from authorities to ensure the right level of compliance in the supply of active pharmaceutical ingredients. You will also respond to complex compliance questions and be responsible for coordinating, planning, and follow up on inspections and audits.
As an Audit and Inspections Coordinator, you will have the following responsibilities:
To succeed in this role, you should have the following qualifications:
Furthermore, you have excellent communication skills with the ability to collaborate, both with internal and external stakeholders.
About the department
You will join the business area of API Quality Assurance Operational and Business Support, which is a part of API Quality. Within this area, you will be a part of the department that drives projects, strategy, audits, and inspections, as well as IT, digitalisation, QA for QC & Manufacturing Development and much more. Our purpose is to set direction within our area of expertise and enable API Quality Assurance to meet our goals.
As a group, we get energy from solving problems, seeing opportunities, and driving impactful change. We focus on development while having fun at the same time; we are maintaining a social work environment with a high level of engagement. Our ambition is to provide world-class support to our key stakeholders, and we take pride in delivering on our commitments. 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 Amalie Nytoft Stjerneby on +45-30775168.
Deadline
28 April 2024
We will be reviewing the applications on an ongoing basis, and we therefore 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 your motivation to apply in your CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to 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 22.2.2024, 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
- Kalundborg
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Statistik over udbudte øvrige i Kalundborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 22. november 2024 | 50 |
| 21. november 2024 | 52 |
| 20. november 2024 | 54 |
| 19. november 2024 | 50 |
| 18. november 2024 | 52 |
| 17. november 2024 | 58 |
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| 14. november 2024 | 60 |
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| 12. november 2024 | 52 |
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| 10. november 2024 | 59 |
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| 8. november 2024 | 60 |
| 7. november 2024 | 57 |
| 6. november 2024 | 57 |
| 5. november 2024 | 57 |
| 4. november 2024 | 50 |
| 3. november 2024 | 52 |
| 2. november 2024 | 53 |
| 1. november 2024 | 53 |
| 31. oktober 2024 | 55 |
| 30. oktober 2024 | 52 |
| 29. oktober 2024 | 53 |
| 28. oktober 2024 | 51 |
| 27. oktober 2024 | 51 |
| 26. oktober 2024 | 52 |
| 25. oktober 2024 | 48 |
| 24. oktober 2024 | 49 |
| 23. oktober 2024 | 48 |