Senior QA Professional
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Kalundborg
Are you looking for an exciting job opportunity as quality responsible working with projects? Do you want to play a vital part in the delivery of Hold a master’s degree within engineering, pharmacy or similar
Have several years’ experience within the pharmaceutical industry, specifically in the field of validation.
You have effective communication and persuasion skills, particularly in english in an international environment.
As a person you are ambitious and ready to be part of our on-going effort to improve our high standards. You dare to challenge us in our way of working and has the desire to take initiative as well as being responsible for your own learning. A proactive mindset is key to succeeding in this role. You are an honest and dedicated team player who inspires and builds trust and respect amongst colleagues and partners. We are cooperating broadly with many stakeholders and therefore excellent collaboration and communication skills are needed. About the department You will join a highly dynamic and well-functioning department in M1 (Manufacturing 1) QA with many interfaces and stakeholders around the organization. The department consists of four teams, and we are supporting M1 (Manufacturing 1), one of the largest API (active pharmaceutical ingredient) factories in Denmark having the hole production process from raw materials to final APIs (active pharmaceutical ingredients). The department has a high level of self-governance, and the working relations are informal. We value good humour and an open and honest culture. We can offer you an exciting and challenging job with committed colleagues in a changing environment. A well-functioning team, where we focus on internal sparring, alignment, and work / life balance. We know that you will develop both your professional and personal competencies, and that you will contribute to the next stage of 's success story. Working at At , we don't wait for change. We drive it. We're a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We are anchored on scientific innovation through the power of our diverse differences. We embrace the spirit of experimentation and strive for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we are all working together to advance patient care. Contact For further information, please contact Manager, Helle Helledie at + . Deadline 10th of November 2024. 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 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.
’s high-quality products to our patients? are you an ambitious and proactive team player who sees collaboration as key to success? Then you might be the colleague we are missing in the quality assurance department of an API (active pharmaceutical ingredient) manufacturing factory, read more and apply now! The position As a Senior QA Professional within validation in our department you will become part of a wonderful team of experienced and engaged QA Professionals bringing expert support to projects and validation activities. Alongside the rest of the team, you will have the responsibility of QA review and oversight of many types of documents, primarily related to validation and qualification. Furthermore, you will ensure quality and compliance with the current GMP rules and guidelines. As a team, we value a great working environment, team spirit and empowerment as well as good development opportunities. Qualifications To succeed in this role, you:
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 18.10.2024, 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.
- 04.11.2024
- Øvrige
- Kalundborg
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Statistik over udbudte øvrige i Kalundborg over tid
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21. november 2024 | 52 |
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4. november 2024 | 50 |
3. november 2024 | 52 |
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1. november 2024 | 53 |
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22. oktober 2024 | 43 |