50 English-speaking jobs in Hillerød

Advanced Product Development Engineer takes technical ownership of medical device design, verification, and robustness from concept to market. Requires experience in design control, risk management, and relevant regulations like ISO 13485 and EU MDR.

Own technical integrity and compliance for medical devices from concept through market life. Drive design-control, risk management, and V&V, turning complex requirements into documented technical choices.

Advanced Product Development Engineer takes technical ownership of medical device design, verification, and robustness from concept through market life. Requires knowledge of design control, risk management, and relevant regulations like ISO 13485 and EU MDR.

Advanced Product Development Engineer to shape primary packaging for next-gen pre-filled syringes. Requires MSc/BSc in relevant science, extensive pharma/medical device packaging experience, and knowledge of regulated environments.

Ymi Sushi seeks a creative Chef/Sushi Chef passionate about Asian cuisine, à la carte, and catering. Responsibilities include daily operations, menu planning, and procurement. Candidates should be proactive, responsible, and service-minded.

QC Scientist needed for Analytical Development to support technology transfer and global product release. Responsibilities include authoring protocols, data analysis, and method support, requiring an MSc/PhD and 5+ years in pharma/biotech.

Seeking IT/OT Quality Specialist for 6-month cover. Support global SOP development, review local procedures, and facilitate process explanations. Requires GxP, CSV, GMP knowledge, and 5+ years experience.

This role drives operational excellence by eliminating waste and improving performance in Finished Goods and Drug Product manufacturing. Responsibilities include leading LEAN initiatives, training, and project management. Candidates need a relevant degree and GMP manufacturing experience.

Support global IT/OT initiatives by writing and reviewing SOPs, WIs, and templates. Requires GMP knowledge, IT/CSV methodologies, and 5+ years experience in computerized system validation.

Coordinate and perform instrument and software qualification across labs, ensuring adherence to cGMP and Data Integrity standards. Drive automation and process enhancement within the QC Instrument Team. Requires 3+ years in cGMP and a relevant degree.

Drive Lean and Continuous Improvement in Finished Goods manufacturing while serving as a Training Partner and project lead for Drug Product initiatives. Focus on waste elimination, operational excellence, and capability building.

Drive IT, equipment, and validation projects from start to finish in Aseptic Manufacturing. Manage a production project portfolio, ensuring new products reach production and compliance is maintained. Requires a Master's degree and 4-5 years of experience.

Join the Deviation Investigation Team for a 1-year assignment. Lead and facilitate deviation investigations to closure, driving root cause analysis and ensuring GMP compliance in a manufacturing environment.

Student Assistant in Maintenance & Metrology supports daily operations through equipment calibration and maintenance. Requires a bachelor's degree in a relevant engineering field and strong English skills.

International Business Manager supporting global sales for process solutions in Grain, Oilseed, Milling, and Feed. Act as an industry expert, consulting with customers and partners to improve operations and profitability.

Responsible and reliable Distribution and Courier Employee needed. Duties include distributing and delivering shipments, measuring districts, planning routes, coordinating activities, and ensuring delivery quality.

Join the QC Analytical Development team to implement chemistry methods for technology transfer and support global product release. Requires MSc/PhD and 5+ years in pharma/biotech, with GXP knowledge.

Build the training setup for a future organization by identifying needs and turning business challenges into practical learning. Design, develop, and implement training content to support onboarding and capability building.

Drive Lean and Continuous Improvement across Finished Goods manufacturing and support Drug Product initiatives as a Training Partner. Focus on waste elimination, operational excellence, and capability building.

Daytime Operators needed for Upstream, Downstream, and Solution Prep at a growing CDMO. Tasks include cGMP document revision, batch documentation, and process execution. Pharmaceutical experience or Life Science graduates are encouraged to apply.