QA scientist with proactive mindset and strong communication skills
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Måløv
Do you want to be part of a fantastic team that values team spirit, empowerment, and good collaboration with our stakeholder? Do you thrive in a constantly changing environment with various challenges and growth opportunities to handle?
We can offer you an exciting job that will match your experience. We look for a self-driven candidate with strong communication skills and solid experience, who is eager to set direction and to ensure compliance, in close work with stakeholders.
You will be part of a team with responsibility for quality assurance for production and packaging of tablets in Oral Finished Product QA (OFP QA). You will influence and set directions in setting the right level of compliance, optimizing our processes by applying a LEAN mindset and establishing new processes.
We can offer a great working environment with high level of team spirit, as well as highly skilled, ambitious, and engaged colleagues. In OFP QA our department consists of colleagues based in both Måløv and Durham US.
The job
You will be trained to become a QP delegate, and you will have the overview of the processes within production of oral medicinal products. In QA we have the quality oversight and are physically present in the production to observe performed processes and help solve issues in real time.
You will perform review of batch documentation as well as review of batch and process related documentation from our stakeholders including deviations, change requests, SOPs etc. Our core task is to ensure that we get products out to our patients at the right quality and in a timely manner.
You will set directions and deliver results which have a significant impact within the context of our business. Your focus will be assuring that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements. You have a risk-based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
We can offer an exciting and challenging position, where you become part of a competent team that acts as sparring partners and problem solvers in quality issues for the production. You will drive optimizations and projects to continue improve processes and the way we work.
Qualifications
We expect that you:
• Hold an academic degree as cand. pharm, cand. Scient, veterinary medicine or similar
• Have solid 5+ years of experience with GMP, quality assurance or production support
• Have strong Project Management experience and examples of dealing with complex projects.
• Solve challenges and take the lead in optimising processes by applying LEAN Tools and principles.
• Are a self-driven and independent person with a high sense of responsibility, who can take initiatives and prioritise your many different tasks.
• Are an open-minded person with high level of energy, an outgoing attitude and have very strong communication and stakeholder management skills.
• Thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders, while taking ownership of your development.
• Have a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity.
As we operate both in a national and an international environment, you must speak and write Danish and English fluently.
About the department
Oral Finished Products QA is a department which employ approximately 60 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.
Contact
For further information, please contact Associate Manager Christina Halberg +45 3075 9031.
We will conduct interviews continually.
Deadline
Deadline to apply for this position is January 9th, 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.
Millions rely on us
To work for Novo Nordisk, you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
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.
Print job Send to e-mail
We can offer you an exciting job that will match your experience. We look for a self-driven candidate with strong communication skills and solid experience, who is eager to set direction and to ensure compliance, in close work with stakeholders.
You will be part of a team with responsibility for quality assurance for production and packaging of tablets in Oral Finished Product QA (OFP QA). You will influence and set directions in setting the right level of compliance, optimizing our processes by applying a LEAN mindset and establishing new processes.
We can offer a great working environment with high level of team spirit, as well as highly skilled, ambitious, and engaged colleagues. In OFP QA our department consists of colleagues based in both Måløv and Durham US.
The job
You will be trained to become a QP delegate, and you will have the overview of the processes within production of oral medicinal products. In QA we have the quality oversight and are physically present in the production to observe performed processes and help solve issues in real time.
You will perform review of batch documentation as well as review of batch and process related documentation from our stakeholders including deviations, change requests, SOPs etc. Our core task is to ensure that we get products out to our patients at the right quality and in a timely manner.
You will set directions and deliver results which have a significant impact within the context of our business. Your focus will be assuring that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements. You have a risk-based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
We can offer an exciting and challenging position, where you become part of a competent team that acts as sparring partners and problem solvers in quality issues for the production. You will drive optimizations and projects to continue improve processes and the way we work.
Qualifications
We expect that you:
• Hold an academic degree as cand. pharm, cand. Scient, veterinary medicine or similar
• Have solid 5+ years of experience with GMP, quality assurance or production support
• Have strong Project Management experience and examples of dealing with complex projects.
• Solve challenges and take the lead in optimising processes by applying LEAN Tools and principles.
• Are a self-driven and independent person with a high sense of responsibility, who can take initiatives and prioritise your many different tasks.
• Are an open-minded person with high level of energy, an outgoing attitude and have very strong communication and stakeholder management skills.
• Thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders, while taking ownership of your development.
• Have a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity.
As we operate both in a national and an international environment, you must speak and write Danish and English fluently.
About the department
Oral Finished Products QA is a department which employ approximately 60 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.
Contact
For further information, please contact Associate Manager Christina Halberg +45 3075 9031.
We will conduct interviews continually.
Deadline
Deadline to apply for this position is January 9th, 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.
Millions rely on us
To work for Novo Nordisk, you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
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.
Print job Send to e-mail
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 9.12.2022, 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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