40 English-speaking jobs in Hillerød

QC Chemist to perform cGMP-compliant analytical testing, method development, and laboratory operations. Requires 4+ years of pharmaceutical industry experience, strong GMP knowledge, and proficiency in various chemistry methods.

Senior Electronics Engineer will own electronics design from concept to production for next-generation analytical instruments. Responsibilities include defining design requirements, leading development across analog and digital domains, and ensuring EMC compliance. Requires solid electronics development experience, a bachelor's or master's degree in electronics engineering, and 5-10 years of experience developing electronic products.

QC Chemist needed for a 12-month maternity cover. The role involves reviewing analytical results, contributing to routine testing, and maintaining equipment. The ideal candidate has a degree in a relevant science discipline and knowledge of analytical chemistry.

Senior Construction Manager to drive delivery of a major infrastructure project. Responsibilities include schedule and cost control, contractor management, risk and change management, and stakeholder coordination. Requires 10+ years experience in complex construction projects.

QA Specialist to review and approve CMMS work orders for maintenance and calibration activities in a GMP regulated biotech environment.

QA Specialist to support deviation management in a regulated biotech environment. Reviews and approves deviations related to testing activities, ensuring compliance with GMP standards.

QA Specialist to support quality oversight of materials and supply chain operations. Reviews and approves deviations, supplier complaints, and ensures compliance with GMP standards. Requires 5+ years of QA experience in a GMP regulated environment.

Hardware Engineer will design and develop production-ready electronics for regulated environments. Experience with low-power design, EMC, and design for manufacturing is required.

Ensures equipment and systems are qualified, compliant, and ready to support operations. Drives qualification activities, supports equipment lifecycle management, and contributes to reliable GMP operations. Focus on qualification of equipment supporting cell bank activities. Collaborates with stakeholders across Production, Quality Assurance, Maintenance, Engineering, IT, and other support functions.

Senior Packaging Design Engineer will lead the design, development, and optimization of carton-based and other paper-based secondary packaging solutions. Responsibilities include leading design, optimizing marketed packaging, creating technical documentation, and collaborating with stakeholders. Requires a Master's degree in Design Engineering or a related field and experience in secondary packaging design and development.

Senior Packaging Design Engineer will lead the design, development, and optimization of carton-based and paper-based secondary packaging solutions. Responsibilities include improving marketed packaging, creating production-ready documentation, and collaborating with global stakeholders.

API Professional will ensure daily support to production within cleaning, sterilization, environmental monitoring, and more. Responsibilities include supporting clean and sterile equipment, ensuring a controlled production environment, and ensuring compliance with regulatory requirements.

Senior Construction Manager to drive delivery of a major infrastructure project. Responsibilities include schedule and cost control, contractor management, risk and change management, and stakeholder coordination. Requires 10+ years experience in construction management on complex projects.

Leads a team of experienced technology transfer leads, overseeing strategy, planning, and execution of tech transfer projects. Ensures robust, compliant, and on-time delivery while collaborating with stakeholders across manufacturing, development, and quality assurance.

As a Quality Assurance, Pharmaceutical Quality System (PQS) Senior Associate, you will lead and support preparations for customer audits and regulatory inspections, ensuring compliance with quality standards. You will collaborate with various departments to strengthen compliance processes and implement improvements.

API Professional supports production within cleaning, sterilization, environmental monitoring, and more. Ensures compliance with regulatory requirements and drives optimization projects. Requires a Master's degree in a related field and at least 2 years of GxP pharmaceutical production experience.

QC Chemist needed for 12-month maternity cover. Responsibilities include reviewing analytical results, contributing to routine testing, and maintaining equipment. Must have a degree in a relevant science discipline and fluency in English. Experience with ICP techniques or GMP environments is advantageous.

Lead the end-to-end transfer, optimization, and implementation of downstream processes into a manufacturing facility. Translate process knowledge into scalable, compliant, and efficient operations, steering activities from new product introduction to validation and continuous improvement.

Leads scientific direction for internal and external communications, bridging innovation with business strategy. Manages a team of scientific professionals and collaborates cross-functionally to support research, regulatory, medical affairs, product development, and commercial teams.

Automation Engineer needed for a pharmaceutical project in Copenhagen. Design, configure, and implement automation systems with a focus on Emerson DeltaV. Troubleshoot, provide support, and collaborate with teams. Bachelor's degree in Automation Engineering, Electrical Engineering, or related field required. Experience with DeltaV and GMP is advantageous.