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The Stability Scientist will manage stability studies, support quality procedures, and collaborate with various stakeholders within the organization and with customers. They will ensure high performance in drug substance production and product release in a dynamic Quality environment.
The Automation Engineer will implement new DeltaV systems to support expansion projects, troubleshoot DeltaV code, review specifications, and collaborate with engineering partners to develop automation solutions. Key responsibilities also include participating in quality activities and ensuring compliance with defined procedures for automation systems.
The GXP Compliance Specialist will support compliance in GMP-related matters within the Supply Chain. Key tasks include managing deviations, supplier complaints, change controls, and ensuring compliance with GMP documents. The role requires coordination with stakeholders and will involve training sessions, audit preparations, and supporting continuous improvement projects.
Seeking a Senior Project Manager for the Strategic Projects team in Hillerod. Responsible for leading and managing CapEx projects in the pharmaceutical and biotech industry, ensuring safe project execution and compliance with regulations. Overseeing project governance, design, construction, safety, and quality activities. Leading projects related to drug product and finished goods areas, as well as technology transfer projects. Joining a team of 8 colleagues and reporting to the Director of Strategic Projects.
The Chromatography Expert/Senior Scientist will be responsible for overseeing chromatographic assays, improving testing processes, ensuring compliance with cGMP standards, and supporting the expansion of QC capabilities. The role involves troubleshooting, method validation, and collaboration within a dynamic team to improve efficiencies in the QC department.
The Global Principal Desktop Engineer is a senior technical role focused on monitoring, managing, and troubleshooting end user computing across the organization. Responsibilities include providing Level 3 support, diagnosing complex technical issues, mentoring junior engineers, and managing client build and software deployment processes.
The Analytical Project Manager will oversee method transfer activities related to Drug Substance and Drug Product testing. Responsibilities include leading meetings, generating transfer plans, and contributing to optimization projects. The role demands effective communication and stakeholder management in a dynamic QC laboratory environment.
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