QA Training Supporter
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Are you interested in playing a key role in ensuring and developing an effective training setup in a fast-growing organisation? Do you want to be part of an engaged and relatively new team that values team spirit, empowerment, and good collaboration with our stakeholder? Then this is could be the right opportunity for you! Read more and apply now. The position
You will be part of the QA support team of approximately 6 highly dedicated employees with different responsibilities. Your main responsibilities will be to:
• ensure the most optimal and easy-to-use training set up for the area
• develop and maintain the training setup to facilitate effective and solid training of our QA colleagues to increase performance and competencies
• support with development of new and existing training content and identification and implementation of training improvements projects
• support management to secure the correct level of competencies of the employees to be in compliance with GMP requirements As part of the role, you will participate in different training networks to be aligned with local and corporate training standards. Additionally, you will be QA implementation lead for different task/projects not necessarily related to training.
Qualifications
We are seeking for a colleague who has a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity. To succeed in this role, you: • hold an academic degree, with a minimum of a bachelor, in a scientific subject
• have at least a couple of years’ experience in a GMP regulated industry
• preferably have experience in quality assurance or production support roles
• are proficient in English As a person you are open minded with high level of energy, an outgoing attitude and have very strong communication and collaboration skills with both your colleagues in QA and the training team in our line of business. You are a dedicated team player who inspires trust and respect among colleagues and partners.
Finally, you are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks. About the department
Emerging Technologies (ET) QA is a new area within Novo Nordisk where the oral portfolio plays a significant role. ET QA has approximately 85 employees and we are growing. 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 part of Novo Nordisk.
Our area is expanding, and we can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. We offer an exciting job opportunity that will match your experience and desire for development. Contact
For further information, please contact Associate Manager Christina Halberg +45 3075 9031.
Deadline
7th August 2023 Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline, so we encourage you to apply sooner later than later. 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 be part of the QA support team of approximately 6 highly dedicated employees with different responsibilities. Your main responsibilities will be to:
• ensure the most optimal and easy-to-use training set up for the area
• develop and maintain the training setup to facilitate effective and solid training of our QA colleagues to increase performance and competencies
• support with development of new and existing training content and identification and implementation of training improvements projects
• support management to secure the correct level of competencies of the employees to be in compliance with GMP requirements As part of the role, you will participate in different training networks to be aligned with local and corporate training standards. Additionally, you will be QA implementation lead for different task/projects not necessarily related to training.
Qualifications
We are seeking for a colleague who has a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity. To succeed in this role, you: • hold an academic degree, with a minimum of a bachelor, in a scientific subject
• have at least a couple of years’ experience in a GMP regulated industry
• preferably have experience in quality assurance or production support roles
• are proficient in English As a person you are open minded with high level of energy, an outgoing attitude and have very strong communication and collaboration skills with both your colleagues in QA and the training team in our line of business. You are a dedicated team player who inspires trust and respect among colleagues and partners.
Finally, you are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks. About the department
Emerging Technologies (ET) QA is a new area within Novo Nordisk where the oral portfolio plays a significant role. ET QA has approximately 85 employees and we are growing. 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 part of Novo Nordisk.
Our area is expanding, and we can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. We offer an exciting job opportunity that will match your experience and desire for development. Contact
For further information, please contact Associate Manager Christina Halberg +45 3075 9031.
Deadline
7th August 2023 Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline, so we encourage you to apply sooner later than later. 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 4.7.2023, 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
- Måløv
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