Opportunité Professionnelle: Senior QA for Quality Control – Microbiology
Présentation de l’Entreprise
Novo Nordisk, reconnu comme un leader mondial dans le domaine des soins de santé, se spécialise dans le traitement des maladies chroniques. Avec plus d’un siècle d’expérience, l’entreprise est animée par une passion pour l’innovation et l’excellence, cherchant à améliorer la vie de millions de patients à travers le monde.
Description du Poste
Titre du poste: Senior QA for Quality Control – Microbiology
Localisation: Gentofte, Hovedstaden, Danemark
Dans ce rôle crucial au sein du département de contrôle qualité (QA), vous serez chargé(e) d’assurer la conformité aux normes de qualité pour la libération de produits pharmaceutiques, ayant un impact direct sur la vie des patients. Le poste implique une collaboration étroite avec les parties prenantes et nécessite une expertise particulière en microbiologie.
Responsabilités Clés
- Direction QA: Établir la direction en matière d’assurance qualité en collaboration avec les parties prenantes.
- Gestion des Écarts: Gérer les Deviation (DVs) et Change Requests (CRs), ainsi que la qualification des nouveaux équipements.
- Collaboration: Assurer une étroite collaboration au sein de l’équipe tout en définissant les priorités des tâches de laboratoire.
- Approbation de SOPs: Garantir que les produits respectent les normes de qualité tout en coordinant les formations nécessaires.
Formation et Environnement de Travail
Les nouveaux employés bénéficient d’un programme de formation structuré et d’un plan de développement individuel pour maximiser leur potentiel. Novo Nordisk attache une grande importance à l’équilibre entre vie professionnelle et vie privée, permettant un travail flexible entre le bureau et le domicile. Le cadre de travail est valorisé pour son informalité et sa culture d’ouverture.
Compétences et Qualifications Requises
- Niveau de formation: Un master dans un domaine pertinent est préféré, bien qu’une expérience significative puisse compenser.
- Expérience: Plus de 5 ans dans le contrôle qualité ou l’assurance qualité dans l’industrie pharmaceutique.
- Intérêt pour la Microbiologie: Compréhension solide de la microbiologie et de ses applications.
- Compétences IT: L’intérêt pour l’informatique dans le contexte QA est un atout.
- Langue: Maîtrise de l’anglais requise.
Culture d’Entreprise et Avantages
Novo Nordisk favorise une culture d’inclusion, accueillant des employés de divers horizons. Les avantages offerts tiennent compte des différentes étapes de la carrière et de la vie personnelle, permettant un développement continu au sein de l’entreprise.
Informations Complémentaires
Pour toute question relative au poste, les candidats intéressés peuvent contacter Misbah Malik, Responsable QA, au +45 3079 5547.
Date limite de candidature: 20 Juillet 2025. Les candidatures sont examinées au fur et à mesure de leur réception.
Ce texte a été rédigé pour refléter des valeurs d’information éthique, tout en détaillant les incontournables de l’opportunité de carrière au sein de Novo Nordisk. Des éléments de vigilance sont intégrés, permettant aux candidats d’évaluer pleinement l’offre.
📅 Date de publication de l’offre : Wed, 09 Jul 2025 03:08:52 GMT
🏢 Entreprise : Novo Nordisk
📍 Lieu : Gentofte, Hovedstaden
💼 Intitulé du poste : Senior QA for Quality Control – Microbiology
💶 Rémunération proposée :
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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Senior QA for Quality Control – MicrobiologyCategory: QualityLocation:Gentofte, Capital Region of Denmark, DKJoin our dynamic QA department as a Quality Control Microbiologist, where your passion for high-quality products will directly impact the lives of patients with chronic diseases. Thrive in a fast-paced environment filled with collaboration opportunities, ensuring the highest quality standards in our microbiology labs.Your new role
In the QA for QC Microbiology role, you will ensure compliance with guidelines for the release of top-quality products by reviewing and approving GMP documents for microbiological test methods and lab equipment. You will also conduct analyses using isolators, autoclaves, and MALDI-TOF, while contributing to the development and validation of microbial methods for new products, and supervising quality activities at our QC laboratories in Gentofte and Bagsværd.Your key responsibilities will include:
- Set the direction from a QA perspective in collaboration with stakeholders. Participate, support and guide QA colleagues.
- Manage Deviations (DVs) and Change Requests (CRs) and qualification of new equipment and validation of new test methods.
- Manage stakeholders to prioritize lab tasks and ensure close collaboration conducting QA Presence.
- Approval of SOPs to ensure products meet quality standards and compliance requirements, and coordinate trainings within the area.
You will undergo a structured and individual training program, and you can expect increasingly more responsibility. You will have an individual development plan to ensure continuous development and realization of your full potential. Equally important, we have a high focus on a great work-life balance, with the flexibility to work from the office and home.Your new department
You will join a team in a highly dynamic, newly established department in Aseptic Manufacturing QA with many interfaces and stakeholders around the organization. Our team supports and oversees quality activities at our QC laboratories, ensuring the highest standards of quality and compliance in all processes.The department has a high level of self-governance, and the working relations are informal. We value good humor and an open and honest culture. We appreciate a colleague who takes responsibility, has a positive and curious approach to new challenges and contributes to a pleasant working atmosphere.Your skills and qualifications
We realize that few people are experts at everything. But if you can nod your head at the following attributes, then you could be the person we are looking for:
- A master’s degree is preferred within the area but it can be compensated by long experience in the field.
- More than 5 years of experience in quality control (QC) or quality assurance and Good Manufacturing Practice (GMP) within the pharmaceutical industry.
- Strong understanding and interest in microbiology and its applications in the pharmaceutical industry.
- It could be a benefit if you have interest in IT from a quality assurance perspective – most of the equipment in the QC labs are computerized equipment
- Proficiency in English is required.
As a person, you have excellent stakeholder management skills and can prioritize lab activities effectively. You are independent, proactive, and detail-oriented, with a strong interest in microbiology. You excel in a collaborative environment and can build strong relationships with team members and stakeholders. You are comfortable working in a high-paced environment and can prioritize tasks.Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.What we offer
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.More information
If you want to know more about the position, please contact QA Manager, Misbah Malik at +45 3079 5547.Deadline
20 July 2025.
Applications are reviewed on an ongoing basis.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.
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