Insud Pharma is a recognised and respected company in the pharmaceutical and healthcare sector with more than 40 years of history and more than 7,000 employees in 50 countries specialising in the research, development, manufacture and marketing of active pharmaceutical ingredients and medicines for human and veterinary use.
Chemo, industrial area of the Insud Pharma group, is a world leader in R&D; and manufacturing of more than 100 value‑added active pharmaceutical ingredients and more than 122 medicines with more than 200 different product presentations. Chemo produces its own active pharmaceutical ingredients (API) as well as finished pharmaceutical products (FDF) covering the main therapeutic groups (Cardiology, Gastroenterology, Central Nervous System, Anti‑infectives, Respiratory, Women's Health, Endocrinology, Dermatology and Urology).
We are looking for a QA TECHNICIAN for our plant, LICONSA
Overview
Assure compliance of GMP, regulatory and internal standards according to quality policies and applicable requirements within the organization. Actively participate in the CAPAs, CCs and complaints management, preparation of PQRs, supplier homologation and update in accordance to internal procedures, GMPs rules, Authorities and customers requirements. EU & US GMP compliance.
General Responsibility
- Raw material suppliers homologation and system maintenance, risk assessment performance. Audits annual plan preparation and support regarding the audit performance. The role is a contact person of the company regarding quality queries to be managed with raw material suppliers or external services.
- Quality complaints from customers: register, investigation and response. Recurrence and tendency identification.
- PQR preparation according to timelines included in the annual plan, internal procedures and TA in force.
- CAPA and CC system: register, evaluation and follow up. Performance of the specific task assigned to.
- Training: GMP basic training to new staff. Register and follow up.
- SOPs: to prepare or update specific SOP related to the activities in charge of.
- Collaborate in external audits from customers and Authorities and conduct shelf‑inspections according to the annual plan.
- Support to Customers and Authorities request for quality and technical issues.
Education
Degree in Pharmacy or Chemistry or Sciences.
Languages
Intermediate or high level of English required and bilingual in Spanish.
Experience (years / area): A minimum of 3 years’ experience in similar position.
Specific Knowledge
Knowledge of EU & US GMPs, quality systems (CAPAs, PQRs, audits support, supplier management, change controls, etc.) in pharmaceutical companies. SAP and Trackwise knowledge is valuable.
COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES
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