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21 jobannoncer matcher din søgning 21 jobannoncer fundet
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Ambitious Project Manager to lead key strategic projects
Are you an experienced Project Manager motivated by making a difference? Then look no further – Pharmacosmos is looking for a Project Manager who can solve complex problems across our value chain and deliver impact to the organisation.
As Project Manager, you will become a key member of a small project management team in Pharmacosmos. You will be allocated to important strategic projects that you will lead and drive to completion to the satisfaction of all involved stakeholders using your existing toolbox and competencies for managing projects.
Kvalitetsleder, Langeland
Sætter du en ære i at levere produkter af høj kvalitet, der altid overholder lovgivning og regler inden for fødevaresikkerhed? Ønsker du at arbejde i en stor fødevarekoncern med kendte danske mærkevarer?
Dine primære opgaver i rollen som kvalitetsleder vil være:
- Vedligeholde og udvikle kvalitetssystemet på fabrikken
- Uddanne og instruere produktionsmedarbejderne i hygiejne og kvalitet
- Ansvar for produktkvalitet i samarbejde med produktionen
QA-specialist, der er QP-delegeret eller drømmer om at blive det
Drømmer du om at bidrage til at sikre kvaliteten af livsvigtige lægemidler, der redder liv? Er du en erfaren kvalitetsspecialist med erfaring fra lægemiddelproduktion?
Som delegeret Qualified Person (QPd) i vores Manufacturing QA (MQA) afdeling får du en unik mulighed for at arbejde med kvalitetssikring og frigivelse af Xellias produkter. Du vil være med til at sikre, at vores antibiotika når frem til patienter i hele verden i den højeste kvalitet. Som delegeret QP hos Xellia får du et stort ansvar.
Specialist, Regulatory Affairs (Temporary Position)
As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.
Further, your main responsibilities include to:
- Gather information and documentation for variation applications
- Update dossier sections
Senior Specialist til QC hos Xellia Pharmaceuticals
Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?
Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.
Senior Medical Writer
Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?
As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.
Department Manager for Molecular Pharmacology
Gubra is seeking a dedicated and experienced Department Manager to lead our Molecular Pharmacology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, along with a background in molecular pharmacology and drug discovery.
Your tasks include
- Daily management of a team of scientists and lab technicians to ensure high performance, personal development, well-being and engagement.
- Guide the team to accomplish department goals and objectives.
- Oversee the planning, execution, and analysis of experiments to support Gubra’s internal and partnered drug discovery projects.
Continuous Improvement Partner
As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.
Your primary tasks will include but not be limited to:
- Develop and sustain CI systems and tools.
- Coach on ideal behaviour that drives a proactive improvement culture.
Trial Product Handling Professional
Do you have a desire to support processes around Trial Product Handling at the clinical sites globally which is essential for the Novo Nordisk’s clinical trials?
Environmental Monitoring Supporter
Do you have an interest in daily operations activities across a manufacturing unit producing lifesaving medicine?
Senior Director, Portfolio Regulatory Policy
Are you passionate about shaping future regulatory frameworks and policies?
GMP Material Scientist
Are you motivated by challenges and thrive in a fast-paced environment?
Clinical Data Standards Specialist
Do you want to work with standardising data in clinical trial?
Corporate Vice President (CVP) Clinical Reporting within Development
Are you a seasoned leader with experience from a large, complex, and international pharmaceutical company?
Development PKPD Specialist
Are you a scientist with flair for mathematical modelling and knowledge of pharmacology, biology or physiology?
Senior Director in Data Orchestration
Can you make a difference in drug development through data?
Senior Manager
Are you an empathetic and empowering leader ready to bring your leadership career to the next level?
Operational Responsible for Storage Facilities
Are you motivated by working in a changing environment?
Clean Utility Engineer
Are you ready to be a part of Novo Nordisk's most significant expansion project in Hillerød?