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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
Associate Sensory scientist/Sensory Panel Lead - Arla Innovation Centre, Aarhus
We are looking for two new Sensory Panel Leads. One new collegue for a 1 year maternity cover and one for a 3 year project. For both positions we hope we will be able to prolong the employment or offer new challenges within Arla Foods.
Your key responsibilities will be:
- In close contact with stakeholders, guide and choose the proper test-setup to deliver the sensory results needed
- Panel training and development of panel competences within specific areas of interest
Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)
At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.
The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.
You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.
Account Manager – Denmark
Actief Hartmanns is searching for an experienced and enthusiastic candidate for the position of Account Manager.
Are you ready to step out of your comfort zone, excel and redefine the limits of what is possible. That’s just what ZEISS employees are doing every single day – in order to set the pace through innovations and enable outstanding achievements. After all, behind every successful company are many great, fascinating people.
Full training in our products, systems and processes is provided. We offer continuous professional development and the opportunity to work as part of a global team with a wide range of career development opportunities.
MS&T Program Manager
We are looking for an experienced professional from the pharmaceutical industry, who can effectively manage project plans across multiple entities and lead cross-functional processes within our own sites and supply chain.
As a MS&T Program Manager, you will be responsible for managing the projects, maintaining project databases, as well as ensuring effective communication and timely achievement of milestones.
Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)
Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!
As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.
Associate Aseptic Manager
Are you ready to take on a challenging role in managing our new production lines?
Microbiologist in Quality Control - Maternity Cover (12 months)
Are you eager to join a fast-growing pharmaceutical company?
Product Specialist - Oral Solid Dosage Forms
Are you passionate about providing expert product knowledge and setting the direction for future tablet production to the benefit of our patients?
QA Validations Professional
Are you interested in joining an exciting journey of innovation that involves implementing new assembly and packaging lines across the globe for Novo Nordisk?
Senior QA Validations Professional
Are you interested in joining an exciting journey of innovation that involves implementing new assembly and packaging lines across the globe for Novo Nordisk?
Validation Specialist
Are you experienced in validation of Finished Product processes within the pharmaceutical industry?
Quality Assurance SME - GxP Regulated Facilities
Novo Nordisk is establishing new, ground-breaking biotech facilities utilizing modern technology with fully automated operations and digitalized processes.