Expert for GLP Quality Assurance
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Søborg
Would you like to leverage your strong Good Laboratory Practice (GLP) knowledge, process optimization skills, and quality-oriented mindset within a highly professional and dynamic global setting, all while having the opportunity to grow and gain experience in the realm of QMS integration projects? Will you bring a ‘can-do’ attitude to support high quality in the development of innovative treatments for patients? Are you eager to dive into an emerging area, with the opportunity to shape its growth and leave a meaningful mark? If so, then take the next step in your journey by joining as GLP QA Expert. Your exciting job opportunity awaits - apply now! About the department GLP QA is one of three sister departments in Research and Development (R&D) Quality Operations, which is part of R&D Quality in . We play a vital role in supporting the non-clinical drug development process to ensure high quality as well as effective fit-for-purpose processes. In , we have an ambitious drug development program, and we are working globally with focus on delivering safe products of high quality that make a difference to patients and ultimately benefit society. We support the development organisation and drive activities such as: Being GLP QA Quality partners to key projects, stakeholders, and line of business Taking part in integration activities when looking at and acquiring new assets Providing GLP QA support globally with tasks such as audit CAPA plans, deviations, change requests, daily support to stakeholders on GLP QA matters Performing vendor assessments Sharing non-clinical quality and GLP knowledge to the global organisation As we also take active part in cross-organisational improvement projects and provide general quality and compliance support to our global organisation, we are on an exciting journey bringing quality on top of the agenda throughout the organisation for the benefit of our patients. The position
The open position is in our GLP QA department, based in Søborg, Denmark. There is a strong need for support in integration activities in potential and actual partnerships and acquisitions. Therefore, we are expanding. Your key areas of responsibility will be: The GLP voice in integration projects, subsequently providing support to ensure the smooth acquisition process of other assets into our process landscape and organisation Responsible for shaping and optimising the framework for the non-clinical quality role in integrations GLP quality partner for a key project/line of business and supporting our stakeholders with GLP advice, work with improvement projects and other department project You will be part of a dynamic area with very experienced and dedicated colleagues within GLP. The position offers high impact, and you are expected to take ownership and responsibility for setting the right quality level in the global organisation. Qualifications
To succeed in this role, you need the following: A Master's degree in science such as biology, pharmacy, medicine or similar Strong knowledge in non-clinical research and drug development 3-5 years of extensive experience in GLP is essential Prior experience in non-clinical quality assurance or GLP QA tasks Preferred qualifications include experience with integration of other assets, although they are viewed as an advantage Proficiency in both written and spoken English
On a personal level, you consistently adopt a constructive and practical approach to problem-solving, demonstrating a keen enthusiasm for optimising and simplifying processes around you. Proactivity and courage characterize your work style, alongside clear communication, and good interpersonal skills. Your organizational ability, paired with a meticulous attention to detail, reflects your ability to maintain a comprehensive perspective on tasks and objectives.
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 embrace the spirit of experimentation, striving 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’re all working to move the needle on patient care. Contact For further information, please contact Ditte Vestergaard at +.
Deadline
31st March 2024. 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 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.
The open position is in our GLP QA department, based in Søborg, Denmark. There is a strong need for support in integration activities in potential and actual partnerships and acquisitions. Therefore, we are expanding. Your key areas of responsibility will be:
To succeed in this role, you need the following:
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 embrace the spirit of experimentation, striving 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’re all working to move the needle on patient care. Contact For further information, please contact Ditte Vestergaard at +.
Deadline
31st March 2024. 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 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 Søborg.
Jobbet er oprettet på vores service den 5.12.2023, 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
- Søborg
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