85 English-speaking jobs in Hillerød

Subject Matter Expert in GMP and facility management needed to drive facility-related changes, develop procedures, and participate in audits and continuous improvement projects.

FUJIFILM Biotechnologies is a world leading Contract Development Manufacturing Organization (CDMO) serving customers in the pharmaceutical industry – from pre-clinical investigations to commercial GMP production. Shape the future of Commercial excellence at FUJIFILM Diosynth Biotechnologies (FLBG).

Experienced CSA Site Manager needed for a flagship critical environment project in Copenhagen. Manage daily site operations, subcontractors, and ensure safe, on-time, and high-quality delivery.

Production Process & Development Specialist will support production and act as a trusted advisor to the management team. Responsibilities include optimizing production processes, driving continuous improvement initiatives, and developing production KPIs. The ideal candidate will have experience in supply chain and/or operations management and a hands-on approach.

Senior Business Analyst to translate business needs into scalable solutions for CRM and commercial tooling. Lead discovery, analysis, and documentation of processes and data flows. Define requirements and solution designs for enhancements and new capabilities. Support system implementations and drive continuous improvement.

Manages global and internal events and webinars, from strategy and planning to execution. Collaborates with marketing, sales, product, and external vendor teams. Responsible for merchandise shop strategy and management.

Student assistant in Strategic Planning & Analytics will support data-driven decision making across Supply Chain organization. Tasks include maintaining dashboards, developing data models, and collaborating with stakeholders.

Drive and improve the material intake process, collaborating with stakeholders across QC, Material/Process Science, Supply Chain, and Purchasing. Identify process improvements, implement changes, and ensure visibility for all stakeholders.

The Product Owner will develop and manage products, ensuring they meet client needs and align with company strategy. Responsibilities include performing product CQAs, leading process gap assessments, and owning product risk assessments. The ideal candidate has a minimum of 5 years of product management experience, preferably in pharmaceuticals, and strong project management and communication skills.

Deliver exceptional guest experiences, ensure product quality, and maintain hygiene standards. Foster a positive work environment, demonstrate dedication, and adhere to company policies and procedures.

Mechanical Quantity Surveyor needed for a data center project in Sweden. Manage cost control for mechanical works, including HVAC, cooling systems, and other infrastructure. Requires a degree in Quantity Surveying, Mechanical Engineering, or related field and 5+ years of experience.

Do you have experience from Visual Inspection and/or other aspects of aseptic drug product manufacturing combined with solid GMP understanding?

Supports onboarding of new products in the visual inspection area, performing manual and automated visual inspection. Assists in equipment/process qualification, validation, and studies. Participates in creating departmental procedures. Requires experience in visual inspection or aseptic drug product manufacturing and GMP understanding.

Leads and manages a team of manufacturing associates across day and night shifts in upstream drug substance manufacturing. Coordinates with shift teams to ensure smooth operations and resolves issues. Implements systems and processes to manage emergencies and minimize downtime.

As we continue to expand, we are looking for a motivated Facility Professional within building construction and facility management who will be an advisor to partners across building expansion projects. The Role and Team Overall, you will be a part of the Facility Group, which consists of 15 people, highly skilled in their respective areas.

Designs, implements, and maintains the automation strategy for Drug Product Manufacturing (D.P.M) equipment and systems. Leads automation workstreams for tech transfers and harmonizes standards. Acts as Subject Matter Expert (SME) for IT-related projects and GMP events.

Support onboarding of new products in the visual inspection area. Perform manual inspection activities and documentation. Assist with equipment/process qualification, validation, and studies.

Supports onboarding of new products in the visual inspection area, performing manual and automated visual inspection. Assists in equipment/process qualification, validation, and studies. Participates in creating departmental procedures. Requires experience in visual inspection or aseptic drug product manufacturing and GMP understanding.

Leads and executes device stability studies to ensure product performance and compliance. Performs trending and data evaluation in LIMS, ensuring accurate documentation. Handles test results, including OOS/OOT investigations. Prepares and maintains protocols, reports, and documentation. Drives implementation of new processes and improvements within stability and quality control areas. Collaborates with cross-functional teams and utilizes digital tools to support a paperless laboratory workflow.

Electronic Engineer to design and develop robust logger systems for extreme environments. Responsibilities include hardware design, firmware development in C/C++, and testing prototypes. Requires a degree in Electronics Engineering, 2-3 years of experience, and proficiency in English.