QUALITY ASSURANCE SUPERVISOR FOR SOFTGELATIN CAPSULES

About us: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).COMMITMENT TO EQUAL OPPORTUNITIESInsud Pharma is aware that business management has to be in line with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current legislation on the subject - Organic Law 3/2007, and we do not discriminate against any person on grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.OverviewEnsure the quality of processes and take the necessary measures to ensure that products manufactured in Liconsa meet the meet the Good Manufacturing Practices for Food Supplements. Investigate deviations, complaints and OOS in order to propose corrective actions and improvements. Research and ensure corrective and preventive as a result of claims, customer audits. Ensure continuous improvement and maintenance of quality of equipment, systems and processes. Comply with the guidelines defined in the Quality Policy, Objectives of the company and with regulations and quality standards of organisms.ResponsabilitiesPResponsible of Quality System Food Supplement management.Coordinate and manage of the specifications of bulk product.Review and approve all master batch records and computer maintenance (validation) in SAP in order to be able to manufacture.Create and maintain Hazard Analysis Critical Control Point (HACCP) documentationCollaborate where necessary that all requirements / requests made by the client are solved.Coordination of the Quality System and customer contact for food supplements products.Elaboration of procedures and bulk product analytical specifications Revision of raw material, bulk and finish product documentation.Change Control management for food supplements productsComplaints management for food supplements products Deviations management for food supplements productsSupplier management: approval and evaluation of suppliers, review and approve all supplier documentationCollaborate in the performance of audits to contract manufacturing Collaborate in the performance of supplier quality audits.Part of shelf inspections audit team.Collaborate in the management of Customer Quality Audits performed on site. CAPA management from Customer Quality Audits, Complaints, Deviation and OOS. QualificationsEducation: Bachelor Degree in Sciences. Languages: High level of English and Spanish. Experience (years/area): A minimum of 5 years’ experience in similar positions. Essential minimum 5 years’ experience in related to manage Quality Assurance systems in production plants pharmaceuticals.Specific Knowledge: Quality Assurance experience. SAP Management, MS Office system.Travels: Willing to travel occasionally. Personal skills: Good communication skills, proactivity, good working under pressure, problem-solving, good organizational skills and persistent.