About this role
Quality Assurance Supervisor - Validação processo at Grupo Medinfar. Location: Coimbra, Coimbra, Portugal. Role: Developing protocols, Reviewing reports, Managing documentation Requirements: 3+ years in pharmaceutical manufacturing; MSc in Pharmaceutical Sciences or Chemical Engineering; GMP/SOP knowledge; Excel proficiency; fluent in English; strong problem-solving and teamwork. Category: Quality Assurance Seniority: Mid Level Tools: Microsoft Excel Commitment: Full Time Workplace: Onsite Languages: English, Portuguese