Químicos farmacéuticos

About the role

Laboratorio LIBRA is seeking qualified Pharmaceutical Chemists to join its Production and Quality Assurance teams. The positions involve ensuring compliance with Good Manufacturing Practices (GMP) and supporting the manufacturing of solid dosage forms in a leading Uruguayan pharmaceutical company.

Key responsibilities

• Execute manufacturing operations for solid pharmaceutical products following GMP standards.
• Maintain and update ERP system data related to production batches.
• Prepare and review technical documentation, including WHO guidelines, ICH, and PICs.
• Support quality assurance activities, including documentation control and basic statistical analysis.
• Collaborate with cross‑functional teams to ensure product quality and regulatory compliance.

Required profile

• Degree in Pharmaceutical Chemistry or related field.
• Minimum two years of experience in solid dosage manufacturing or pharmaceutical industry.
• Strong knowledge of GMP and ERP systems.
• Advanced proficiency in English.

Required skills

• Good Manufacturing Practices (GMP)
• ERP system usage
• Advanced English language skills
• Technical documentation handling (WHO, ICH, PICs)
• Basic statistical methods

What we offer

• Opportunity to work in a reputable, 60‑year‑old national pharmaceutical leader.
• Professional development within a dynamic, team‑oriented environment.