Recipharm in Queluz

Located in Lisbon, Portugal, Recipharm’s Queluz facility is a flexible, multi‑purpose development and manufacturing site supporting human and veterinary pharmaceutical products. With capabilities spanning liquid, semi‑solid and solid dosage forms, and high-potency handling capabilities, the Queluz site plays an important role in Recipharm’s European manufacturing network.

Site Capabilities

Development & manufacturing expertise

• Production of liquid, semi‑solid and solid dosage forms
• Specialist capabilities for effervescent tablet manufacturing
• Flexible operations supporting both human and veterinary medicines

High‑potency handling

• OEB4 capability (1–10 µg/m³) for safe handling of potent compounds
• Suitable for a broad range of high‑potency pharmaceutical applications

Integrated services across Recipharm’s global network

The Queluz site connects customers to Recipharm’s wider service offering, including:

• High‑potency manufacturing
• Semi‑solid manufacturing
• Liquid formulation and manufacturing
• Solid dose manufacturing services

Quality, compliance & regulatory readiness

Global regulatory approvals

The Queluz site is inspected and approved by leading regulatory authorities, including:

• Approved by Infarmed in line with EU‑GMP
• ANVISA (Brazil)
• SFDA (Saudi)
• U.S. FDA
• Licensed for human and veterinary drug manufacturing and controlled drug handling

Certified Management Systems

The site operates in line with the following ISO aligned quality systems:

• ISO 14001 – Environmental Management
• ISO 45001 – Occupational Health & Safety

Sustainability Commitment

• EcoVadis Gold rating, demonstrating Recipharm’s strong ESG and sustainability commitment

Careers at Recipharm Queluz

Explore opportunities at Recipharm’s Queluz facility and join a global CDMO network committed to high‑quality pharmaceutical development and manufacturing.

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