Corporate Quality Assurance Technician 1 | Di-921

Detalles de la oferta

Mission: Collaborate in the implementation of the Quality Manual in the affiliates and collaborate in the audit plan for manufacturers, subsidiaries, distributors, licensees, CROs, and logistics operators.Functions Quality system management: claims, change control, deviations, and CAPAs.Review and approval of Corporate Areas documentation: Pharmacovigilance, Clinical, Toxicology, Regulatory, HR, IT, Purchasing, Supply & Operations, Marketing, R&D, Laboratory (SOPs, validations, transfers, specifications, analytical methods, change control, manufacturing methods, deviations, CAPAs).External audits: of GMPs (Good Manufacturing Practices) services of finished product manufacturers, packaging material, external microbiological and analytical labs, licensees and distributors, GLP (Good Laboratory Practices) of CROs for safety and efficacy in-vitro studies, GCP (Good Clinical Practices) of CROs for in vivo and clinical studies, GDP (Good Distribution Practices) for storage and transport and GVP (Good Pharmacovigilance Practices) of CROs for pharmacovigilance services.Internal Audits: to Corporate Areas and subsidiaries.Collaborate in the implementation of the Quality System of the subsidiaries (review of procedures).Writing/Reviewing Quality Agreements.Review of manufacturing documentation and batch control of subcontracted manufacturers for release to the market.Computerized Systems Validation.Requirements Education: University degree in Pharmacy, Biology, Chemistry, Engineering or Health Sciences.Experience: At least 5 years in Production or Quality of active ingredients or pharmaceutical products, in development or industrial scale. GMPs domain.Languages: English and Spanish proficiency (read, spoken and written).IT: Office programs.Desired Education: Training in Quality Systems. Knowledge in ISO 9001, ISO 13485 (Medical Device), ISO 22716 (Cosmetics). Knowledge in GDPs, GLPs, GCPs, GVP.Experience: in Audits, cosmetics, food supplements, pesticides, microbiology, injectables, and medical devices. Experience in corporate/international Quality organizations.Languages: Other languages (e.G. French, German, Italian, Portuguese, Chinese).IT: ERP (e.G. SAP), Documental Systems (e.G. Documentum, Qumas), Quality Systems (e.G. Trackwise).Others: Decision-making capability, autonomy, team-working, orientation to detail.#J-18808-Ljbffr


Salario Nominal: A convenir

Fuente: Jobtome_Ppc

Requisitos

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