Hire Pharmaceutical Experts Across Europe | Moving2Europe.eu

Global Recruitment for Pharmacologists, Regulatory Specialists, QC Analysts & GMP Technicians

With Europe’s pharmaceutical industry leading global innovation in drug development, manufacturing, and clinical research, demand for skilled professionals continues to grow. From API production in Poland to clinical trials in Germany and regulatory support in the Netherlands, qualified pharmaceutical talent is essential for operational success and compliance.

At Moving2Europe.eu, we specialise in sourcing and placing certified pharmaceutical professionals with strong scientific backgrounds, GMP training, and global experience across the entire pharma lifecycle—from R&D to distribution.

Why Choose Moving2Europe.eu for Pharmaceutical Recruitment?

• 16+ years of expertise in pharma and life sciences recruitment
• Access to a vetted global pool of pharmacists, QA/QC professionals, and formulation experts
• Talent with EU pharmaceutical compliance experience (EMA, GMP, GDP, ISO 9001)
• Professionals trained in laboratory analysis, batch release, regulatory documentation, and pharmacovigilance
• End-to-end visa, relocation, and onboarding support for EU and non-EU hires

Pharmaceutical Roles We Recruit

We help employers fill positions such as:

• Formulation Scientists
• Pharmaceutical Production Operators
• Quality Control Analysts
• Pharmacovigilance Specialists
• Regulatory Affairs Experts
• Clinical Trial Assistants
• GMP Manufacturing Technicians
• Pharmacists & Pharmacy Assistants
• Validation Engineers
• QA/QC Managers

Organisations We Support

We supply pharmaceutical talent for:

• API and Drug Manufacturers
• Contract Research Organisations (CROs)
• Contract Manufacturing Organisations (CMOs)
• Clinical Trial Units
• Pharmaceutical Packaging Firms
• Hospital and Retail Pharmacies
• Biopharmaceutical Companies
• Regulatory and Compliance Consultancies

Global Talent Sourcing with EU Pharmaceutical Compliance

Our recruitment pipeline spans across regions with deep scientific and pharma training:

• EU Nationals –
  • Germany, Portugal, Czech Republic – Experienced in EU pharma regulations and GMP procedures
• South Asia:
  • India, Nepal, Sri Lanka – Highly qualified formulation scientists, production staff, and pharmacovigilance analysts
• Southeast Asia:
  • Philippines, Vietnam, Indonesia – Skilled lab technologists, quality assurance testers, and pharma logistics professionals
• Sub-Saharan Africa:
  • Ghana, Kenya, Nigeria – QA/QC staff and pharmacists with multilingual capabilities
• North Africa:
  • Egypt, Tunisia, Morocco – Trained GMP technicians and validation engineers with EU migration readiness
• Eastern Europe & Balkans:
  • Ukraine, Moldova, Georgia – Research chemists and regulatory documentation experts
• Gulf Region & Third-Country Nationals –
  •  Licensed pharmacists and pharmaceutical engineers working in Gulf-based multinationals
• Latin America:
  • Brazil, Colombia, Cuba, Dominican Republic – Clinical support staff and pharmaceutical researchers

What Sets Our Pharmaceutical Candidates Apart?

• Technical Expertise: Solid knowledge of GMP, GDP, GLP, and ISO standards
• Hands-on Skills: Equipment calibration, documentation, quality audits, batch release, and lab analytics
• Certifications: Trained in EMA and FDA-compliant processes, pharmacovigilance systems, and validation protocols
• Language & Communication: Fluent in English and often additional EU languages for multinational collaboration
• Industry Versatility: Competent in generics, OTC, biosimilars, and speciality pharma

Our Pharmaceutical Hiring Process

1. Define your project scope, skill requirements, and regulatory needs
2. Identify and screen qualified candidates through technical interviews and compliance verification
3. Support all visa, relocation, and onboarding documentation
4. Ensure EU-compliant placement, cultural alignment, and job-readiness
5. Provide integration support for lab and production environments

Build Reliable Pharmaceutical Teams with Global Talent

At Moving2Europe.eu, we help pharmaceutical manufacturers, CROs, and research hubs build world-class teams to ensure regulatory success and product excellence. Whether it’s drug discovery, clinical support, or QA audits—our candidates are trained, certified, and ready to deliver.

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Frequently Asked Questions (FAQs)

1. What types of pharmaceutical roles do you recruit for?

We recruit across manufacturing, QA/QC, R&D, regulatory, packaging, and clinical operations.

2. Are your candidates trained in GMP and pharmaceutical compliance?

Yes. Our talent pool includes GMP-certified professionals and compliance-focused staff.

3. Do you supply regulatory affairs specialists?

Absolutely. We provide professionals with experience in EMA submissions and EU compliance.

4. Can you help staff clinical trial support teams?

Yes. We recruit clinical trial assistants, pharmacovigilance officers, and documentation specialists.

5. Do your candidates have experience with international pharma firms?

Many have worked for global manufacturers and follow EMA and FDA guidelines.

6. Are multilingual professionals available?

Yes. We offer candidates fluent in English, German, French, Polish, Dutch, and more.

7. Can I hire temporary staff for audits or short-term projects?

Yes. We offer flexible recruitment for full-time, contract, and interim staffing.

8. How quickly can candidates be mobilised?

Typically, within 3–5 weeks, depending on role complexity and visa requirements.

9. What locations do you support within Europe?

We recruit for pharmaceutical projects across Germany, France, Austria, Poland, the Netherlands, and other EU countries.

10. How do I begin hiring pharmaceutical professionals?

Just Register Now, and we’ll match you with certified pharma experts.