Luxembourg offers a central location within Europe, making it an ideal hub for multinational pharmaceutical and scientific companies. Its proximity to major European markets supports international collaboration and business growth.
The Luxembourg government actively supports the science and pharmaceutical sectors through funding, research grants, and tax incentives. Public-private partnerships help foster innovation and technological advancement.
Luxembourg has been investing heavily in biotechnology, health sciences, and pharmaceutical research. The presence of research centers like the Luxembourg Institute of Health and the University of Luxembourg strengthens the sector's foundation.
Professionals working in Luxembourg benefit from excellent healthcare, education, and safety. The high standard of living attracts top talent from around the world.
Luxembourg is a multilingual country with English widely used in business and research. Its international environment makes it easier for professionals to integrate and collaborate across cultures.
The country offers competitive compensation packages in the science and pharmaceuticals industry. Employees often receive comprehensive benefits, including health insurance and generous leave policies.
Luxembourg encourages sustainable and innovative research in pharmaceuticals and life sciences. This forward-thinking approach helps attract researchers and companies committed to impactful work.
Luxembourg’s science and pharmaceutical sectors emphasize cutting-edge research in areas like precision medicine, biotechnology, and digital health. International candidates can contribute to pioneering projects supported by advanced technology and interdisciplinary collaboration.
The country fosters strong ties between academia and industry. Institutions such as the University of Luxembourg and the Luxembourg Institute of Health collaborate with global pharmaceutical companies, offering international talent access to both academic research and industrial application.
Luxembourg's workforce is highly international, creating an inclusive environment for scientists from around the world. English is widely spoken in professional settings, making it easier for international candidates to adapt and contribute effectively.
International researchers and professionals benefit from national funding schemes and innovation programs aimed at attracting global talent. These initiatives support scientific exploration and career development.
With its strategic location in the heart of Europe, Luxembourg provides a gateway to European Union markets. International professionals in science and pharmaceuticals have the opportunity to work on projects with continental and global impact.
Luxembourg encourages skill development through training programs, conferences, and innovation hubs. International professionals can build long-term careers with potential for mobility across the EU.
The country offers streamlined visa processes and attractive residency options for qualified professionals in science and pharmaceuticals. This makes relocation smoother and more appealing for international candidates seeking long-term opportunities.
Professionals in this role conduct laboratory and clinical research in areas such as biotechnology, molecular biology, immunology, and pharmacology. They are often employed by research institutes, universities, and pharmaceutical companies.
These experts ensure that pharmaceutical products comply with local and international regulations. They play a critical role in preparing documentation for clinical trials and product approvals.
CRAs manage and monitor clinical trials to ensure compliance with regulatory standards and scientific protocols. They are essential for bringing new treatments from development to market.
These professionals maintain high product standards by overseeing testing processes, inspecting manufacturing practices, and ensuring compliance with Good Manufacturing Practices (GMP).
These roles involve analyzing complex biological and clinical data to support research outcomes, drug development, and public health decisions. Data scientists are increasingly vital in health tech and digital pharma.
Experts in this area promote pharmaceutical products to healthcare professionals, develop marketing strategies, and conduct market analysis to drive product adoption.
Medical writers create scientific documents such as clinical study reports, regulatory submissions, and research publications. Their work supports drug development and communication with regulatory bodies.
These professionals design and improve processes for manufacturing pharmaceutical and biotech products. Their role includes scaling up lab-based procedures to industrial production levels.
These roles involve monitoring and assessing the safety of pharmaceutical products once they are on the market, ensuring adverse effects are identified and managed appropriately.
Lab technicians perform routine tests, maintain lab equipment, and support research activities in both public research institutions and private companies.
They serve as the link between pharmaceutical companies and the medical community, providing scientific support and ensuring ethical communication of product information.
These professionals coordinate cross-functional teams and manage timelines, budgets, and resources for research or product development projects. They are key to successful project delivery in science-based industries.
Job Profile |
EUR (€) |
USD ($) |
INR (₹) |
|---|---|---|---|
|
Research Scientist |
€75,000 |
$82,500 |
₹6,900,000 |
|
Clinical Research Associate (CRA) |
€65,000 |
$71,500 |
₹5,980,000 |
|
Regulatory Affairs Specialist |
€72,000 |
$79,200 |
₹6,624,000 |
|
Quality Assurance Analyst |
€68,000 |
$74,800 |
₹6,256,000 |
|
Quality Control Analyst |
€62,000 |
$68,200 |
₹5,704,000 |
|
Biostatistician |
€70,000 |
$77,000 |
₹6,440,000 |
|
Data Scientist (Life Sciences) |
€78,000 |
$85,800 |
₹7,176,000 |
|
Medical Science Liaison |
€80,000 |
$88,000 |
₹7,360,000 |
|
Pharmacovigilance Officer |
€66,000 |
$72,600 |
₹6,072,000 |
|
Drug Safety Specialist |
€64,000 |
$70,400 |
₹5,888,000 |
|
Regulatory/Medical Writer |
€60,000 |
$66,000 |
₹5,520,000 |
|
Pharmaceutical Sales Representative |
€55,000 |
$60,500 |
₹5,060,000 |
|
Marketing Manager (Pharma) |
€85,000 |
$93,500 |
₹7,820,000 |
|
Project Manager (Life Sciences) |
€82,000 |
$90,200 |
₹7,544,000 |
|
Process Development Scientist |
€74,000 |
$81,400 |
₹6,808,000 |
|
Biotech Engineer |
€70,000 |
$77,000 |
₹6,440,000 |
|
Laboratory Technician |
€50,000 |
$55,000 |
₹4,600,000 |
|
Microbiologist |
€62,000 |
$68,200 |
₹5,704,000 |
|
Biomedical Engineer |
€68,000 |
$74,800 |
₹6,256,000 |
|
Medical Affairs Manager |
€90,000 |
$99,000 |
₹8,280,000 |
Eligibility Criteria |
Details |
|---|---|
|
Educational Qualifications |
Bachelor’s, Master’s, or PhD in relevant fields (e.g., biology, chemistry, pharmacy, biotech, biomedical sciences) |
|
Work Experience |
1–5 years for junior to mid-level roles; 5–10+ years for senior or specialized positions |
|
Language Requirements |
English is widely accepted; knowledge of French, German, or Luxembourgish is a plus |
|
Work Visa / Residence Permit |
Required for non-EU/EEA applicants; employer usually sponsors a work visa |
|
Recognition of Qualifications |
Non-EU degrees may need validation through Luxembourg’s Ministry of Higher Education |
|
Professional Licensure |
Required for regulated professions (e.g., pharmacists); may require EU equivalence |
|
Technical Skills |
Laboratory techniques, GMP compliance, clinical research, data analysis, bioinformatics, etc. |
|
Soft Skills |
Communication, teamwork, critical thinking, attention to detail |
|
Job Offer from Luxembourg Employer |
Mandatory to apply for a work visa |
|
Health Insurance |
Must be covered under Luxembourg’s national health insurance once employed |
|
Background Check / References |
Common requirement, especially in clinical and regulatory roles |
|
Language Certification (if applicable) |
May be required if French or German is a job requirement |
Job Profile |
General Roles and Responsibilities |
|---|---|
|
Research Scientist |
Design and conduct experiments, publish findings, collaborate on research projects |
|
Clinical Research Associate (CRA) |
Monitor clinical trials, ensure regulatory compliance, manage trial documentation |
|
Regulatory Affairs Specialist |
Prepare and submit regulatory documents, ensure product compliance with local and EU regulations |
|
Quality Assurance (QA) Analyst |
Implement quality systems, conduct audits, ensure GMP and SOP compliance |
|
Quality Control (QC) Analyst |
Perform laboratory tests, validate processes, maintain product quality records |
|
Biostatistician |
Analyze clinical data, design statistical models, support trial planning and reporting |
|
Data Scientist (Life Sciences) |
Extract and analyze biomedical data, develop predictive models, support digital health initiatives |
|
Medical Science Liaison (MSL) |
Act as a scientific advisor, engage with healthcare professionals, support medical education |
|
Pharmacovigilance Officer |
Monitor drug safety, manage adverse event reports, ensure regulatory reporting |
|
Drug Safety Specialist |
Assess drug risks, prepare safety reports, support risk management strategies |
|
Medical Writer |
Create scientific documents (clinical reports, regulatory submissions), simplify complex information |
|
Regulatory Writer |
Write regulatory documentation, ensure alignment with EU guidelines and submission standards |
|
Pharmaceutical Sales Representative |
Promote pharmaceutical products, meet healthcare providers, drive product sales |
|
Marketing Manager (Pharma) |
Develop marketing strategies, analyze market trends, manage product launch campaigns |
|
Project Manager (Life Sciences) |
Coordinate cross-functional teams, manage budgets, timelines, and deliverables |
|
Process Development Scientist |
Optimize manufacturing processes, scale lab protocols, ensure product consistency |
|
Biotech Engineer |
Design biotechnological processes and equipment, support production and R&D |
|
Laboratory Technician |
Perform lab tests, maintain equipment, record results for analysis and research |
|
Microbiologist |
Study microorganisms, conduct contamination tests, ensure biological safety in products |
|
Biomedical Engineer |
Design medical devices, support diagnostics, collaborate with clinicians on technical solutions |
Job Profile |
Educational Qualification |
Experience (Years) |
Key Skills Required |
|---|---|---|---|
|
Research Scientist |
Master’s/PhD in Biology, Chemistry, Biotech |
2–5+ |
Experimental design, data analysis, scientific writing |
|
Clinical Research Associate (CRA) |
Bachelor’s/Master’s in Life Sciences, Pharmacy |
1–4 |
GCP compliance, clinical trial monitoring, documentation |
|
Regulatory Affairs Specialist |
Bachelor’s/Master’s in Pharmacy, Regulatory Affairs |
2–5 |
EU regulations, dossier preparation, communication |
|
Quality Assurance Analyst |
Bachelor’s in Life Sciences, Pharmacy, QA certification |
2–4 |
GMP, SOPs, audits, compliance |
|
Quality Control Analyst |
Bachelor’s in Chemistry, Biotech, or Microbiology |
1–3 |
Lab testing, instrumentation, data integrity |
|
Biostatistician |
Master’s/PhD in Biostatistics, Mathematics |
2–5 |
Statistical modeling, SAS/R, clinical data analysis |
|
Data Scientist (Life Sciences) |
Master’s in Bioinformatics, Data Science, or similar |
2–6 |
Python, R, machine learning, biomedical data handling |
|
Medical Science Liaison (MSL) |
PharmD/PhD in Medicine or Life Sciences |
3–6 |
KOL engagement, scientific communication, medical education |
|
Pharmacovigilance Officer |
Bachelor’s/Master’s in Pharmacy or Medicine |
1–4 |
Drug safety monitoring, case processing, risk management |
|
Drug Safety Specialist |
Bachelor’s/Master’s in Pharmacy, Medicine, Life Sciences |
2–5 |
Adverse event reporting, MedDRA, safety databases |
|
Medical Writer |
Master’s/PhD in Life Sciences |
2–6 |
Scientific writing, clinical documentation, regulatory knowledge |
|
Regulatory Writer |
Bachelor’s/Master’s in Life Sciences or Journalism |
2–5 |
Technical writing, EMA/FDA guidelines, document formatting |
|
Pharmaceutical Sales Representative |
Bachelor’s in Pharmacy, Life Sciences, Business |
1–3 |
Product knowledge, sales tactics, communication |
|
Marketing Manager (Pharma) |
MBA + Science Degree (preferred) |
4–8 |
Market analysis, branding, campaign development |
|
Project Manager (Life Sciences) |
Master’s in Science/Engineering + PMP (optional) |
3–7 |
Project planning, team coordination, budget tracking |
|
Process Development Scientist |
Master’s in Biotech, Biochem, Chemical Engineering |
3–6 |
Process optimization, scaling, lab-to-production transfer |
|
Biotech Engineer |
Bachelor’s/Master’s in Biotech or Biomedical Engineering |
2–5 |
Bioprocessing, automation, equipment design |
|
Laboratory Technician |
Bachelor’s/Diploma in Lab Technology or Sciences |
0–3 |
Sample preparation, lab maintenance, basic testing |
|
Microbiologist |
Bachelor’s/Master’s in Microbiology |
1–4 |
Sterility testing, contamination control, pathogen ID |
|
Biomedical Engineer |
Bachelor’s/Master’s in Biomedical Engineering |
2–5 |
Medical device design, clinical interface, compliance |
Job Profile |
Entry-Level Experience |
Mid-Level Experience |
Senior-Level Experience |
|---|---|---|---|
|
Research Scientist |
0–2 years |
3–6 years |
7+ years |
|
Clinical Research Associate (CRA) |
1–2 years |
3–5 years |
6+ years |
|
Regulatory Affairs Specialist |
1–3 years |
4–6 years |
7+ years |
|
Quality Assurance Analyst |
1–2 years |
3–5 years |
6+ years |
|
Quality Control Analyst |
0–2 years |
3–4 years |
5+ years |
|
Biostatistician |
1–2 years |
3–6 years |
7+ years |
|
Data Scientist (Life Sciences) |
1–3 years |
4–6 years |
7+ years |
|
Medical Science Liaison (MSL) |
2–3 years |
4–6 years |
7+ years |
|
Pharmacovigilance Officer |
1–2 years |
3–5 years |
6+ years |
|
Drug Safety Specialist |
1–2 years |
3–5 years |
6+ years |
|
Medical Writer |
1–3 years |
4–6 years |
7+ years |
|
Regulatory Writer |
1–3 years |
4–6 years |
7+ years |
|
Pharmaceutical Sales Representative |
0–2 years |
3–5 years |
6+ years |
|
Marketing Manager (Pharma) |
3–5 years |
6–8 years |
9+ years |
|
Project Manager (Life Sciences) |
2–4 years |
5–7 years |
8+ years |
|
Process Development Scientist |
2–4 years |
5–7 years |
8+ years |
|
Biotech Engineer |
1–3 years |
4–6 years |
7+ years |
|
Laboratory Technician |
0–2 years |
3–4 years |
5+ years |
|
Microbiologist |
1–2 years |
3–5 years |
6+ years |
|
Biomedical Engineer |
1–3 years |
4–6 years |
7+ years |
Company Name |
Industry Focus |
International Hiring Notes |
|---|---|---|
|
Hôpitaux Robert Schuman |
Clinical Research, Public Health |
Hires researchers, lab staff, and clinicians; English often accepted |
|
Luxembourg Institute of Health (LIH) |
Biomedical Research, Epidemiology |
Actively recruits international PhD/postdocs; English-speaking |
|
University of Luxembourg |
Academic Research, Life Sciences |
Offers positions for researchers, lecturers, and postdocs globally |
|
Paul Wurth (SMS Group) |
Biotech Engineering, Process Tech |
Hires engineers and scientists; focuses on innovation and R&D |
|
Aposave (part of Bionical Emas) |
Clinical Trials, Pharma Services |
International talent welcome; English is main language |
|
Sanofi |
Pharmaceuticals, Drug Development |
Global company with local presence; hires for regulatory and R&D roles |
|
B Medical Systems |
Biomedical Devices, Cold Chain |
Recruits international engineers and researchers |
|
Laboratoires Réunis |
Diagnostics, Pathology, Genomics |
Open to international lab staff and researchers |
|
Eurofins Scientific |
Testing, Genomics, Bioanalytics |
Luxembourg HQ; hires international candidates in lab and IT functions |
|
HITEC Luxembourg S.A. |
Health Tech, Engineering |
Multidisciplinary; open to international applicants |
|
DSM-Firmenich |
Nutrition, Biotech, Life Sciences |
Recruits globally for R&D and production roles |
|
Ketterthill Laboratories |
Medical Diagnostics |
Hires lab technicians, analysts, and biomedical scientists |
|
Pfizer (Regional Roles) |
Pharmaceuticals, Clinical Research |
Open to international scientists and regulatory experts |
|
Amplexor Life Sciences (now part of IQVIA) |
Regulatory Services, Pharma IT |
Recruits globally for regulatory and documentation roles |
|
Arendt Regulatory & Consulting |
Pharma Compliance, Regulatory Affairs |
Hires international legal-scientific profiles |
|
ExcellGene (partner site roles) |
Bioprocessing, Cell Line Development |
Collaborative projects in Luxembourg, hires globally |
|
Fast Track Diagnostics (Siemens Healthineers) |
Infectious Disease Diagnostics |
Multinational team; open to international lab and R&D roles |
|
Clearstream (Deutsche Börse Group) |
Pharma Data & Compliance |
Hires data scientists and analysts in regulated pharma environments |
|
NBE-Therapeutics (Boehringer Ingelheim) |
Antibody-Drug Conjugates, Oncology |
Luxembourg-based research roles for international scientists |
|
Charles River Laboratories |
Preclinical and Clinical Testing |
International roles in toxicology, pathology, and lab sciences |
Job Profile |
Avg. Salary (€/Year) |
Job Requirements |
Roles & Responsibilities |
Top Hiring Companies |
|---|---|---|---|---|
|
Research Scientist |
€75,000 |
PhD or Master’s in Life Sciences, research experience |
Conduct lab research, analyze data, publish findings |
LIH, University of Luxembourg, Eurofins |
|
Clinical Research Associate (CRA) |
€65,000 |
Bachelor’s/Master’s in Life Sciences, GCP knowledge |
Monitor clinical trials, ensure regulatory compliance |
Aposave, IQVIA, Sanofi |
|
Regulatory Affairs Specialist |
€72,000 |
Bachelor’s/Master’s in Pharmacy or Regulatory Affairs |
Prepare and submit regulatory filings, ensure product compliance |
Amplexor (IQVIA), Arendt, Sanofi |
|
Quality Assurance Analyst |
€68,000 |
Bachelor’s in Life Sciences, knowledge of GMP/SOPs |
Ensure product quality, conduct internal audits, maintain documentation |
Laboratoires Réunis, Eurofins, DSM-Firmenich |
|
Quality Control Analyst |
€62,000 |
Bachelor’s in Chemistry/Microbiology, lab experience |
Perform routine testing, calibrate equipment, validate methods |
Ketterthill, B Medical Systems, Fast Track Diagnostics |
|
Biostatistician |
€70,000 |
Master’s/PhD in Biostatistics or Mathematics |
Analyze clinical data, design trial protocols, support publications |
LIH, University of Luxembourg, IQVIA |
|
Data Scientist (Life Sciences) |
€78,000 |
Master’s in Data Science/Bioinformatics |
Analyze complex biological data, develop predictive models |
Clearstream, Eurofins, DSM-Firmenich |
|
Medical Science Liaison (MSL) |
€80,000 |
PharmD/PhD, strong medical communication skills |
Liaise with healthcare professionals, present clinical data |
Pfizer, Sanofi, Boehringer Ingelheim |
|
Pharmacovigilance Officer |
€66,000 |
Bachelor’s/Master’s in Pharmacy or Medicine |
Monitor drug safety, manage adverse event reports |
IQVIA, Aposave, LIH |
|
Drug Safety Specialist |
€64,000 |
Bachelor’s in Life Sciences, MedDRA knowledge |
Safety reporting, signal detection, regulatory communication |
Charles River Labs, Aposave |
|
Medical Writer |
€60,000 |
Master’s/PhD in Life Sciences, writing proficiency |
Draft clinical trial reports, regulatory documents, and publications |
IQVIA, Amplexor, University of Luxembourg |
|
Regulatory Writer |
€60,000 |
Life Sciences or Journalism degree, regulatory knowledge |
Write documentation for submissions (EMA/FDA), format per guidelines |
Arendt, Amplexor, Charles River Labs |
|
Pharma Sales Representative |
€55,000 |
Bachelor’s in Pharmacy or Life Sciences, sales skills |
Promote products to doctors/pharmacists, meet sales targets |
Sanofi, Pfizer, B Medical Systems |
|
Marketing Manager (Pharma) |
€85,000 |
MBA or equivalent + Science background |
Develop strategies, manage campaigns, analyze product performance |
DSM-Firmenich, Sanofi, Pfizer |
|
Project Manager (Life Sciences) |
€82,000 |
Master’s in Science or Engineering, PMP preferred |
Coordinate teams, manage budgets/timelines, risk management |
Paul Wurth, Eurofins, IQVIA |
|
Process Development Scientist |
€74,000 |
Master’s in Biotech, Biochem, or Chemical Engineering |
Scale lab processes, optimize production workflows |
DSM-Firmenich, B Medical Systems, Eurofins |
|
Biotech Engineer |
€70,000 |
Bachelor’s/Master’s in Biotech or Biomedical Engineering |
Design biotechnological systems, optimize equipment and production processes |
Paul Wurth, DSM-Firmenich, B Medical Systems |
|
Laboratory Technician |
€50,000 |
Bachelor’s/Diploma in Lab Technology or Sciences |
Perform lab tests, maintain instruments, prepare samples |
Laboratoires Réunis, Ketterthill, Fast Track Diagnostics |
|
Microbiologist |
€62,000 |
Bachelor’s/Master’s in Microbiology |
Test for microbial contamination, ensure lab hygiene and safety |
LIH, Eurofins, Ketterthill |
|
Biomedical Engineer |
€68,000 |
Bachelor’s/Master’s in Biomedical Engineering |
Develop medical devices, work with clinical teams, ensure technical compliance |
B Medical Systems, Siemens Healthineers, Paul Wurth |
Visa Type |
Eligibility |
Key Features |
Suitable For |
|---|---|---|---|
|
EU Blue Card |
Non-EU nationals with a job offer & higher education degree |
Fast-track residence permit, high salary threshold, renewable, EU mobility |
Highly qualified professionals (scientists, engineers, etc.) |
|
Salaried Worker Permit |
Non-EU nationals with a valid job contract from a Luxembourg employer |
Standard work visa, renewable, linked to employer |
General science, pharma, lab tech roles |
|
Researchers Permit |
Non-EU researchers with a hosting agreement from a public research institution |
Designed for academic/research professionals, allows research-specific residence |
Postdocs, PhD researchers, institutional scientists |
|
Intra-Company Transfer (ICT) Permit |
Employees transferred from a non-EU branch of a multinational company |
Short/long-term stays, applicable for managers/specialists |
Senior pharma or biotech professionals in global companies |
|
Short-Term Work Visa |
Job duration under 90 days (contract, conference, trial project, etc.) |
Valid for short-term assignments or research collaborations |
Guest researchers, consultants, trainers |
|
Self-Employed Permit (Limited Use) |
Business founders or freelance consultants in scientific or technical services |
Requires business plan and approval from the Ministry of Economy |
Consultants, freelance researchers (less common) |
|
Student to Work Transition |
Non-EU students graduating from a Luxembourg university |
Can apply to stay after graduation for job search (up to 9 months) |
Recent graduates in life sciences or biotech fields |
|
Family Reunification Visa |
Family members of a foreign worker or researcher in Luxembourg |
Allows spouse and children to reside and potentially work |
Spouses of professionals with valid work permits |