37 English-speaking jobs in Hillerød

Senior Secondary Packaging Engineer, Product Responsible Device Delivery Solutions (DDI), Secondary Packaging Hillerød, Denmark Teaser There has never been a more exciting time to work within Secondary Packaging at Novo Nordisk.

If you enjoy transforming regulatory and quality requirements into practical engineering solutions, coordinating technical activities across stakeholders, and delivering documentation that enables confident decision-making, then you could be our next Senior Product Development Engineer.

Risk Coordinator - Pharmaceutical Project Risk Coordinator – Pharmaceutical Project Working hours: 40 hours per week Start: As soon as possible Assignment duration: Until 28 February 2027 About the position Solvexis Consult is looking for an experienced Risk Coordinator to support a pharmaceutical project during turnover, commissioning, qualification and validation (CQV).

Risk Coordinator - Pharmaceutical Project Full time | Solvexis Consult | Denmark Posted On Job Information Job Opening Status In-progress Construction Work Experience 4-5 years City Hillerød State/Province Sjælland Job Description Risk Coordinator – Pharmaceutical Project Working hours: 40 hours per week Start: As soon as possible Assignment duration: Until 28 February 2027 About the positio

# Secondary Packaging ResponsibleAnsøg hos virksomheden## JobbeskrivelseSenior Secondary Packaging Engineer, Product ResponsibleDevice Delivery Solutions (DDI), Secondary PackagingHillerød, DenmarkTeaserThere has never been a more exciting time to work within Secondary Packaging at Novo Nordisk.

Do you enjoy coordinating across teams, keeping things moving and spotting opportunities to develop the business? We are looking for a Sales Support & Business Development Specialist to join our Indirect Sales team in Denmark.

Lead a senior team to set direction and ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, planning, and execution while standardizing best practices.

Senior IT Systems Analyst for QC Applications manages Labware LIMS and Empower operations. Responsibilities include system maintenance, vendor coordination, and driving optimization projects while ensuring GxP compliance.

Support Quality & Compliance in a fast-paced production environment. Responsibilities include handling deviations, performing shopfloor walks, and maintaining SOP accuracy, requiring cGMP experience.

Lead the Bioreactor Scale-Up team, setting global vision using expertise in cell culture process modeling and simulation. Drive projects from bench to production scale while serving as a primary customer contact.

Lead and drive ServiceNow deliverables end-to-end, managing platform operations and global adoption. Partner to build the roadmap, handle 2nd level support, and perform configuration tasks.

Lead end-to-end drug substance tech transfer into large-scale manufacturing. Drive compliant introduction of clinical, PPQ, and commercial processes, partnering with internal teams and customers. Requires 8+ years in CMC process development/GMP.

Experienced Validation Engineer/SME needed for Controlled Temperature Units (CTUs) like refrigerators. Drive validation strategy, ensure regulatory compliance, and lead IQ/OQ/RQ activities within the life science industry.

Why this role matters Build once, scale everywhere: Create end-to-end designs that harmonize IT/OT, secure data flows, and enable resilient site operations across multiple facilities and modalities. Raise the bar on compliance and speed: Surface risks and dependencies early, align to enterprise patterns, and get solutions release-ready with fewer surprises and less rework.

Manage and validate PLM, CAD, and CAE systems like CATIA and Windchill for Drug Delivery Innovation. This role involves system administration, project delivery, user support, and ensuring compliance.

Experienced Validation Engineer/SME needed to drive validation for Controlled Temperature Units (CTUs) like refrigerators. Requires 8+ years in pharma/biotech, deep knowledge of GMP, and expertise in IQ/OQ and risk management.

Doctoral Candidate position to evaluate enterovirus surveillance, conduct seroprevalence studies on biobank samples, and build data-driven models of population susceptibility. Requires a Master's in biomedical sciences or related fields.

Doctoral candidate vacancy to evaluate multicenter surveillance of enterovirus infections. The role involves building data-driven models and conducting seroprevalence studies using biobank samples. A Master's degree in a relevant field is required.

Architect the digital backbone for GxP Manufacturing, translating complex needs into scalable IT/OT solutions. Ensure security and compliance across MES, DCS/SCADA, and cloud systems. Requires 8+ years in relevant architecture.

Seeking an experienced Validation Engineer/SME for Controlled Temperature Units (CTUs). Drive validation strategy, own lifecycle, and ensure compliance with global regulatory requirements.