Releasing advanced QA Professional
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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? 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. We are looking for a senior QA professional like you, with a high level of dedication, and an innovative mindset, who thrives in a constantly changing and challenging environment. The Position You will be part of the QA releasing team in OFP QA. Your main responsibility will be review of batch documentation, release in your role as QP delegate and QA approval of several different types of documents and processes related to the daily operation for bulk production of tablets in Oral Finished Product QA (OFP QA). 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 influence and set directions in setting the right level of compliance, optimizing our processes by applying a LEAN mindset and establishing new processes. 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. 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. Qualifications We seek a colleague who fits our team both professionally and personally. 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 production. You hold an academic degree within MSc in Pharmacy, veterinarian or similar, this to ensure you fulfil the requirements from the Danish Medicine Agency to “Qualified Person”. You have 3+ years of experience with GMP, quality assurance or production support. You are an open-minded person with high level of energy, an outgoing attitude and have very strong communication and collaboration skills. You are a dedicated team player who inspires trust and respect among colleagues and partners. You are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks. You 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 70 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 Linea Frenk Alsing +45 3075 6596. Deadline Deadline to apply for this position is July 31st 2023. Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline. 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.
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 25.4.2023, 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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