About this role
QA Corporate_Documentation Specialist (0, 0, 0) at HIPRA | Building Immunity for a Healthier World. Location: Amer, Catalonia, Spain. Role: drafting documents, maintaining documents, validating systems Requirements: Bachelor's in engineering/pharmacy/chemistry/biology, GMP training, 3+ years in similar regulated roles, technical English, experience with regulatory documentation, inspections, and audited environments. Category: Quality Assurance Seniority: Mid Level Tools: SmartPlant, QDOC Certifications: gmp Commitment: Full Time Workplace: Onsite Languages: English, Spanish