2464 English-speaking jobs in Copenhagen

Safety Surveillance Specialist to lead analytical and medical evaluation of aggregate safety data in CVD clinical development. This role shapes safety profiles and drives benefit-risk assessments. Requires a Master's in Medicine or Natural Sciences and experience in drug development.

Associate Director in RA CMC Semaglutide (maternity cover) leads teams, ensures compliance, and drives regulatory strategies for Semaglutide products. Requires 8+ years in drug development with 3+ in leadership.

Area Training Partner strengthens operational performance and compliance through training. Requires 2+ years in learning/training, stakeholder management, and data analysis. Partners with teams to guide GxP-compliant training setups.

Define and lead the strategic effectiveness framework for paid media investment globally. Own MMM and econometric analysis to translate complex data into actionable investment decisions.

Define and drive the AI strategy for Product & Portfolio Strategy, translating priorities into a focused AI agenda. Shape the AI operating model, govern the portfolio, and ensure value realization across global operations.

Drive sales growth by developing territory and account plans across drug modalities like Biologics and API. Requires 5-8 years of quota-carrying sales experience and strong scientific and commercial acumen.

Guide a team of application scientists supporting proteomics advances. Provide pre- and post-sales technical support, training, and consultative services. Manage complex scientific workflows and collaborate with sales teams.

Prepare, review, and coordinate local regulatory submissions for clinical trials, aligning with global strategy. This role requires a Bachelor's degree and relevant experience, focusing on regulatory compliance and coordination.

The (Associate) Medical Director provides medical support and advice for clinical trials and safety evaluation within Pharmacovigilance. Requires MD, MB/BS, clinical experience in Neurology, and pharmaceutical industry experience.

Senior Director of Qualitative Data Collection and Analysis leads QDA projects, managing data collection, vendor relations, and qualitative research technologies. This role develops QDA business plans and builds a research center of excellence.

Senior Technical Sales Specialist for Single-Use Technologies drives revenue and pipeline growth. Requires 7+ years in bioproduction sales, a life-science degree, and strong technical sales skills.

(Senior) Medical Director for Nephrology, EMEA. Provides medical support and advice for clinical trials and safety evaluation. Requires MD with Nephrology specialty and industry experience in clinical development.

Field Service Engineer performs on-site installation, alignment, and repair of sophisticated equipment. Responsibilities include system validation, customer advising, and conducting maintenance for analytical instruments. Travel up to 75% is required.

Lead the EMEA Human Identification (HID) sales organization to drive growth. This role requires an experienced commercial leader with a strong understanding of forensics and genomics to develop regional sales strategies and build high-performing teams.

(Senior) Medical Director for Rheumatology, EMEA, provides medical support and advice for clinical trials and safety evaluation within Pharmacovigilance. Requires an MD specializing in Rheumatology with clinical experience.

Develop the Cell Culture, Cell Therapy & Supplements business in the Nordics. Focus on upstream bioprocesses, developing business for the Gibco portfolio. Requires life science degree and sales experience in biotechnology.

Act as the bridge between business and technology, guiding AI use cases from discovery to value realization. Partner with leaders to translate business challenges into scalable AI solutions.

Lead the people side of AI transformation, driving behavioral change and business value across a global organization. Own upskilling programs, drive tool adoption, and build an AI adoption ecosystem.

Coordinate production planning across multiple lines and stakeholders, ensuring material and capacity availability. Support daily execution, manage changes, and improve planning processes in a complex manufacturing environment.

Laboratory Technician in Peptide Research synthesizes and purifies modified peptides. Requires knowledge of organic synthesis, peptide chemistry, HPLC, and LC-MS for analysis and data interpretation.