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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
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.
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.
Delegated QP for QA Finished Goods Manufacturing
We are looking for an experienced delegated Qualified Person (QP) to join our successful QA team supporting Finished Goods Manufacturing (FGM).
Manufacturing Project Supporter
We’re in search of our new team-mate for the role of Manufacturing Project Supporter, to join the Manufacturing Support Department in Hillerød!
Upstream Support Specialist
Would you like be responsible for providing technical assistance within process design and process documentation?
Microbiologist in Quality Control - Maternity Cover (12 months)
Are you eager to join a fast-growing pharmaceutical company?
Scientist for QC Raw Materials Analytical Management Team
We are looking for a scientist that understands the quality setup of a QC laboratory in a GMP environment.
Instrument Maintenance Coordinator for QC Instrument Support
Are you a good coordinator with a big picture mind-set and “can-do” attitude who thrives in an environment where close collaboration involving multiple stakeholders is key?
