83 English-speaking jobs in Hillerød

Develop, validate, and improve test methods for device and primary packaging development. Lead validation activities, ensure method robustness, and coach colleagues on measurement practices. Act as a subject matter expert, guiding project teams on test method development and validation.

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.

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.

Are you passionate about upholding quality standards in a rapidly evolving industry? Do you have the expertise to drive excellence and innovation in pharmaceutical quality systems?

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.

SAP Functional Architect needed for Supply Chain. Experience with SAP configuration in MM, PP, and QM modules required. 5-10 years of operation and maintenance of SAP IT systems, preferably in the pharmaceutical industry. Strong stakeholder management and communication skills. Fluency in English required.

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

Are you interested in working in a pharmaceutical Contract Development and Manufacturing organization and gain experience within GMP? Do you have an interest in product quality? Then you should consider this student job in our team, as a student assistant in QA for Materials & Supply Chain.

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.

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. Must have 5-10 years of experience in SAP IT systems, preferably in the pharmaceutical industry. Strong business process analysis and redesign skills are essential. Fluency in English is required.

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.

Leads global marketing strategy and execution for FOSS Go, a new portfolio targeting a new customer segment. Responsible for brand strategy, channel strategy, and community strategy. Drives hybrid marketing approaches, including digital acquisition and offline activation. Collaborates with sales, SSS, distributors, and key account teams.

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.

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.

The Construction Handover Coordinator will lead and assist with facility handovers from construction to daily operations. Responsibilities include managing clean rooms during Care, Custody & Control, coordinating access control, and overseeing building maintenance.

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.