GMP Partner
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
Køge
Are you ready to make an impact in the pharmaceutical industry? Join our team at Novo Nordisk Pharmatech in Køge as a GMP Partner and play a vital role in ensuring the highest quality standards for our manufacturing processes. If you thrive in a dynamic environment, possess strong problem-solving skills, and have a passion for quality, we want to hear from you!Apply now for a life-changing career!The position
As a GMP Partner, you will have a wide range of responsibilities to support our manufacturing operations and maintain compliance with Good Manufacturing Practices (GMP). The position will refer directly to the Director of Manufacturing, allowing you to provide strategic direction to the manufacturing management group regarding quality matters.In the job, you can look forward to preparing quality activity plans for manufacturing, as well as assisting process owners in creating and maintaining a system to establish appropriate requirements for investment projects, ensuring optimal outcomes. Your other key duties will include:• Active participation in audits/inspections, providing guidance and coaching to employees involved in presenting during these activities.
• Preparing and presenting the annual Quality Management Review, summarizing key quality metrics, trends, and improvement initiatives.
• Being the KPI Champion: Driving the department's Quality Management System (QMS) Key Performance Indicators (KPIs) related to deviations, change requests, and Quality Activity Plans (DV, CR, QAP, etc.).
• Conducting a thorough three-year review of Standard Operating Procedures (SOPs) and developing a systematic approach to enhance planning and efficiency.
• Utilizing a systematic and analytical approach to drive the reduction of deviations, implementing corrective and preventive actions.You will also take ownership of the Manufacturing Process Landscape, collaborating closely with the production training supporter to establish and maintain a clear understanding of the manufacturing process landscape, ensuring compliance and efficiency. You will participate in and potentially lead cross-functional problem-solving initiatives, promoting a culture of continuous improvement.Qualifications
To excel in the role of GMP Partner, you should have:• Some years of experience in a GMP-regulated environment.
• Academic education in a relevant field, with a master's degree preferred. However, a bachelor's degree combined with significant experience or technical education will also be considered.
• Proficiency in Lean methodologies and strong problem-solving abilities to drive process improvements.
• Fluency in English and good communication skills in Danish or another Scandinavian language, to effectively collaborate with various stakeholders across the organization.You will thrive in the job if you have an outgoing and approachable personality, coupled with excellent communication and interpersonal skills.About the department
The Manufacturing organisation of Novo Nordisk Pharmatech A/S consists of app. 85 employees in 7 teams. The Manufacturing organization is responsible for production, technical support, process support, project execution, and facility management. In the position as GMP Partner, you are required to work closely together with the management team.Working at Novo Nordisk Pharmatech A/S
Novo Nordisk Pharmatech A/S has 300+ employees and is 100% owned by Novo Nordisk A/S. The ability of Novo Nordisk Pharmatech A/S to produce and deliver quality products to the pharmaceutical industry, combined with our complete range of services within regulatory requirements, makes us a preferred supplier to many global pharmaceutical companies. Novo Nordisk Pharmatech A/S is a fast-growing company, which is generating many exciting projects and excellent development opportunities.Contact
For further information please contact Manufacturing Director, John Halfdan Boiesen, at +45-30370020.Deadline
6 August 2023.Applications will be screened on an ongoing basis, and we regularly call for interviews.
Please do not hesitate to apply, by simply uploading 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.
As a GMP Partner, you will have a wide range of responsibilities to support our manufacturing operations and maintain compliance with Good Manufacturing Practices (GMP). The position will refer directly to the Director of Manufacturing, allowing you to provide strategic direction to the manufacturing management group regarding quality matters.In the job, you can look forward to preparing quality activity plans for manufacturing, as well as assisting process owners in creating and maintaining a system to establish appropriate requirements for investment projects, ensuring optimal outcomes. Your other key duties will include:• Active participation in audits/inspections, providing guidance and coaching to employees involved in presenting during these activities.
• Preparing and presenting the annual Quality Management Review, summarizing key quality metrics, trends, and improvement initiatives.
• Being the KPI Champion: Driving the department's Quality Management System (QMS) Key Performance Indicators (KPIs) related to deviations, change requests, and Quality Activity Plans (DV, CR, QAP, etc.).
• Conducting a thorough three-year review of Standard Operating Procedures (SOPs) and developing a systematic approach to enhance planning and efficiency.
• Utilizing a systematic and analytical approach to drive the reduction of deviations, implementing corrective and preventive actions.You will also take ownership of the Manufacturing Process Landscape, collaborating closely with the production training supporter to establish and maintain a clear understanding of the manufacturing process landscape, ensuring compliance and efficiency. You will participate in and potentially lead cross-functional problem-solving initiatives, promoting a culture of continuous improvement.Qualifications
To excel in the role of GMP Partner, you should have:• Some years of experience in a GMP-regulated environment.
• Academic education in a relevant field, with a master's degree preferred. However, a bachelor's degree combined with significant experience or technical education will also be considered.
• Proficiency in Lean methodologies and strong problem-solving abilities to drive process improvements.
• Fluency in English and good communication skills in Danish or another Scandinavian language, to effectively collaborate with various stakeholders across the organization.You will thrive in the job if you have an outgoing and approachable personality, coupled with excellent communication and interpersonal skills.About the department
The Manufacturing organisation of Novo Nordisk Pharmatech A/S consists of app. 85 employees in 7 teams. The Manufacturing organization is responsible for production, technical support, process support, project execution, and facility management. In the position as GMP Partner, you are required to work closely together with the management team.Working at Novo Nordisk Pharmatech A/S
Novo Nordisk Pharmatech A/S has 300+ employees and is 100% owned by Novo Nordisk A/S. The ability of Novo Nordisk Pharmatech A/S to produce and deliver quality products to the pharmaceutical industry, combined with our complete range of services within regulatory requirements, makes us a preferred supplier to many global pharmaceutical companies. Novo Nordisk Pharmatech A/S is a fast-growing company, which is generating many exciting projects and excellent development opportunities.Contact
For further information please contact Manufacturing Director, John Halfdan Boiesen, at +45-30370020.Deadline
6 August 2023.Applications will be screened on an ongoing basis, and we regularly call for interviews.
Please do not hesitate to apply, by simply uploading 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 Køge.
Jobbet er oprettet på vores service den 24.7.2023, 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
- Køge
Lignende jobs
-
HVAC Process Engineer
Do you dream about making an impact on patients worldwide? Are you ready to join a team of highly skilled colleagues and work in a fast-paced environment? Then you might be our new HVAC Process Eng..Få mere info- Øvrige
- Kalundborg
-
Kvalitets- og bæredygtighedsansvarlig søges
Har du evner og lyst til at være ansvarlig for kvalitetssikring en i virksomhed, der arbejder fokuseret med stålprojekter på byggepladser hovedsageligt på Sjælland? Trives du i en hverdag, som tage..Få mere info- Øvrige
- Gørlev
-
Distriktskoordinator
Om jobbet Til [xxxxx]s teknisk drift og service søges pr. 1. november 2024, eller snarest derefter 1 driftskoordinator. Den gennemsnitlige ugentlige arbejdstid er 37 timer. Stillinge..Få mere info- Øvrige
- Kalundborg
-
IT System Manager
Do you get motivated by driving IT System Management for critical IT systems in a complex stakeholder landscape? Are you ready to play a key role in maintaining IT compliance and the validation of .Få mere info- Øvrige
- Kalundborg
Statistik over udbudte jobs som øvrige i Køge
Herunder ser du udviklingen i udbudte øvrige i Køge over tid. Bemærk at jobs der ikke har en bestemt geografi ikke er medtaget i tabellen. I den første kolonne ser du datoen. I den næste kolonne ser du det samlede antal øvrige.
Se flere statistikker her:
Statistik over udbudte øvrige i Køge over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 21. september 2024 | 43 |
| 20. september 2024 | 43 |
| 19. september 2024 | 39 |
| 18. september 2024 | 41 |
| 17. september 2024 | 37 |
| 16. september 2024 | 38 |
| 15. september 2024 | 34 |
| 14. september 2024 | 39 |
| 13. september 2024 | 39 |
| 12. september 2024 | 38 |
| 11. september 2024 | 39 |
| 10. september 2024 | 38 |
| 9. september 2024 | 35 |
| 8. september 2024 | 35 |
| 7. september 2024 | 37 |
| 6. september 2024 | 35 |
| 5. september 2024 | 26 |
| 4. september 2024 | 26 |
| 3. september 2024 | 26 |
| 2. september 2024 | 25 |
| 1. september 2024 | 28 |
| 31. august 2024 | 30 |
| 30. august 2024 | 30 |
| 29. august 2024 | 30 |
| 28. august 2024 | 26 |
| 27. august 2024 | 26 |
| 26. august 2024 | 25 |
| 25. august 2024 | 29 |
| 24. august 2024 | 29 |
| 23. august 2024 | 28 |
| 22. august 2024 | 28 |