102 English-speaking jobs in Hillerød

Student assistant will review and analyze quality records, conduct trend reviews, assist with report creation, and support colleagues with tasks. Must have a bachelor's degree or be finishing one in Pharmaceutical – Biotechnology Engineering/Sciences or a related field.

Manage and ensure compliance with quality standards on a fast-paced project. Prepare quality documentation, lead site inspections, and liaise with the client quality team.

Senior QA Specialist to provide quality oversight for QC laboratory activities. Responsibilities include reviewing and approving QC documentation, changes, deviations, instrument qualifications, and tech transfers.

Leads and hosts customer audits and regulatory inspections, ensuring compliance with PQS/QMS frameworks (ICH Q10/Q9, EU GMP, 21 CFR 210/211/11). Collaborates with stakeholders to strengthen compliance processes and implement improvements. Supports maintenance and continuous improvement of the PQS, including deviation/CAPA quality, change control, risk management, and training effectiveness. Monitors regulatory intelligence and drives updates to procedures and training.

Senior QA for QC Specialist will provide QA support to the QC laboratory, reviewing and approving QC-related documentation, changes, and instrument qualifications. Responsibilities include quality approval of work orders and alarms, ensuring procedures are followed, and acting as a quality partner by providing guidance and training.

Lead and support preparations for customer audits and regulatory inspections at the Hillerød site. Coordinate audit/inspection readiness, including mock inspections, scripting, SME coaching, and data integrity. Lead audit responses, align with stakeholders, prepare and track CAPA plans, and ensure effectiveness verification. Collaborate with QA, Manufacturing, QC, Supply Chain, Regulatory Affairs, and Business Process Owners to strengthen compliance processes. Support maintenance and continuous improvement of the PQS aligned to ICH Q10 and ICH Q9. Ensure ongoing compliance with applicable regulations and standards. Track and report metrics related to audit closure timelines, CAPA effectiveness, and critical/major/minor finding rates.

This student assistant role in Quality Assurance for Materials & Supply Chain supports Product Quality Reviews, including reviewing quality records, trend reviews, report creation, and ad hoc tasks. Requires a bachelor's degree in Pharmaceutical - Biotechnology Engineering/Sciences or a related field, proficiency in Microsoft Office, and strong English communication skills.

QA Compliance Operations Lead/Coordinator will represent the QA Director, coordinate audit readiness, and drive quality improvements.

SAP Functional Architect needed for Supply Chain. Experience with SAP MM, PP, and QM modules required. 5-10 years of experience in SAP IT systems, preferably in the pharmaceutical industry. Strong business process analysis and redesign experience. Must have excellent stakeholder management and communication skills. Fluency in English is required.

QA Compliance Operations Lead/Coordinator will represent the QA Director, coordinate audit and inspection readiness, and drive quality improvements.

This student assistant role in Quality Assurance for Materials & Supply Chain supports Product Quality Reviews, including reviewing quality records, trend reviews, report creation, and ad hoc tasks. Requires a bachelor's degree in Pharmaceutical - Biotechnology Engineering/Sciences or a related field, proficiency in Microsoft Office, and strong English communication skills.

Leads and scales EET Group's Professional Audio Visual & Display business across Europe. Responsible for revenue growth, EBITDA performance, and portfolio value creation. Manages vendor relationships, Go-to-Market strategies, sales enablement, and inventory management. Reports to the Chief Product & Solutions Officer.

Senior Quality Assurance Professional will provide quality oversight of the Primary Packaging and Combination Product development process, reviewing and approving development documentation. The role involves interpreting regulatory requirements, guiding projects from inception to product launch, and collaborating with stakeholders.

This hands-on role combines customer support, operational execution, and technical service delivery in a global IoT environment. Responsibilities include resolving customer connectivity issues, coordinating with internal and external teams, and contributing to operational stability.

OT Cybersecurity Engineer needed to maintain OT cybersecurity solutions, analyze system behavior, respond to security alerts, and train system admins. Requires a bachelor's degree, 5+ years in OT roles, 1 year in OT cybersecurity, and experience with security solutions software.

SAP Functional Architect needed for Supply Chain. Experience with SAP MM, PP, and QM modules required. 5-10 years of experience operating and maintaining SAP IT systems, preferably in the pharmaceutical industry. Strong business process analysis and redesign experience. Fluency in English required.

Experienced Deviation Investigator needed to lead end-to-end investigations in a cGMP biopharmaceutical manufacturing environment. Classify production occurrences, perform root-cause analysis, write deviation reports, and develop CAPAs. Collaborate with production teams to ensure timely batch release.

Senior Business Analyst to translate business needs into scalable solutions for CRM and commercial tooling. Will partner with Commercial stakeholders and BT&DS delivery teams to drive clarity, alignment, and governance. Experience with CRM platforms, commercial tooling, and regulated environments required.

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

The Field Test Coordinator plans and executes field tests at customer sites globally, ensuring customer readiness and coordinating logistics. This role involves collecting test data, documenting observations, and providing feedback to the R&D team.