Analytical Professional - Quality Control
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Måløv
Are you ready to provide high-quality analytical results and work with multiple stakeholders to steer future work processes within our exciting department at Approve analytical results and oversee analytical methods Ensure GMP compliance and implement requirements Participate in inspections and audits Align with business targets Manage deviations and laboratory investigations We are committed to ensuring a smooth onboarding process for new employees. During the initial days, you will spend time with other new team members, participating in an engaging introduction program. The Department Manager will provide a warm welcome, and a colleague will act as a mentor guiding you through your individual training plan. Qualifications We are looking for someone with: A degree as a Pharmacist, Chemist, or in a similar life sciences discipline - whether you've just graduated or already have some professional experience, we would be happy to hear from you Ideally, you have some experience in a laboratory or related roles within a GMP-regulated environment with deviations, laboratory investigations, and change requests Proficiency in both written and spoken English and Danish As an individual, you thrive in a flexible environment, and your adaptability ensures success in a role where the quality of your work is paramount. You approach tasks in a structured manner, maintaining an unwavering focus on quality. Your dedication, positive attitude, and proactive approach enable you to actively contribute to various problem-solving scenarios and foster a healthy working environment. Furthermore, you need to have good communication and stakeholder management skills as you will play an important role in driving continuous process improvements. About the DepartmentYou will be joining one of the teams in our QC department (Market Release) within Emerging Technology, which comprises 5 teams of approximately 80 employees in total. We are responsible for delivering reliable analytical results in a timely manner and providing analytical support to our customers. Our oral products are utilized by patients worldwide, and we continuously strive to improve and optimize our processes while implementing new technologies. The workplace is in Måløv.Working at At , we do not wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we understand that what brought us to where we are today might not necessarily guarantee future success. We embrace the spirit of experimentation, aiming for excellence without fixating on perfection. We never shy away from opportunities to develop; we seize them. From research and development to manufacturing, marketing, and sales, we all work to make a difference for millions of patients living with chronic diseases. Join us! Together, we’re life changing. ContactFor further information, please contact Kasper Drejsanger at: Deadline 08 April 2025 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.
? Do you have a quality-oriented mindset and a passion for ensuring GMP compliance? If so, we invite you to explore this exciting opportunity with us! We are seeking two committed and enthusiastic colleagues to join teams in our QC department . Read more and apply for a life-changing career with us today! The position You will play an important part in providing high-quality analytical results and steering future work processes within our QC department (Market Release) in Emerging Technology. You will be responsible for ensuring optimal performance of analyses and applying LEAN principles to troubleshoot and enhance our working procedures. Your contributions will significantly impact Novo Nordisk’s tablet production. You will:
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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 25.3.2025, 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.
- 25.03.2025
- Øvrige
- Måløv
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