Descripción de la oferta
Department and Location:Quality Control; Intas B2B DivisionOn-site, Barcelona Metropolitan AreaOverall objectiveSince its inception in March 2005, Intas B2B has established itself as a trusted pharmaceutical licensor, delivering over 150 finished products to more than 100 partners across EMEA, APAC, Canada, and LATAM. To support this strategic initiative, we are seeking a Senior QC Analyst to perform quality control testing activities in compliance with company SOPs, internal policies, and applicable regulatory requirements, in alignment with approved Marketing Authorization dossiers. This role will contribute to ensuring the quality, safety, and compliance of pharmaceutical products by executing analytical testing, documenting results, and supporting routine quality control operations.Key ResponsibilitiesPerform routine and non-routine analytical testing in accordance with approved methods, specifications, and GMP requirements.Review and verify analytical data, ensuring accuracy, completeness, and compliance with data integrity principles.Prepare and review analytical documentation, including Certificates of Analysis (CoAs), test records, SOPs and laboratory worksheets.Ensure compliance with internal SOPs, work instructions, and applicable regulatory requirements during all laboratory activities.Support the investigation of deviations, Out of Specification (OOS) and Out of Trend (OOT) results, contributing to root cause analysis and implementation of CAPAs.Support Change Control activities related to laboratory processes, methods, equipment, and materials.Organize and maintain laboratory operations, including management of laboratory supplies and purchasing, coordination of workflows, equipment oversight, and control of samples and reference standards.Identify, evaluate, and select suppliers for laboratory consumables and reagents, ensuring cost-effectiveness, quality, and compliance with company standards.Core CompetenciesStrong attention to detail and commitment to quality.Analytical and critical thinking skills.Problem-solving and decision-making abilities.Effective communication and collaboration skills.Strong organizational and time management skills with the ability to handle multiple priorities.Proactive mindset with a continuous improvement approachRelevant Functional/ Technical Skills or Industry ExperienceHigher Vocational Training (Ciclo Formativo de Grado Superior) in Analytical Laboratory, Chemistry, or a related field.Minimum of 4–5 years of experience in a Quality Control laboratory or Analytical Development within the pharmaceutical industry.Hands-on experience in analytical techniques (HPCL, GC, TD, KF.. etc) and laboratory testing under GMP conditions.Solid understanding of EU GMP and regulatory requirements applicable to Quality Control.Experience working with solid oral dosage forms is highly desirable.Experience in data review, data integrity principles, and laboratory documentation.Good level of English, particularly in reading and writing.What We OfferOpportunity to be part of a strategic expansion project with high visibility.Dynamic and collaborative work environment.Competitive salary and benefits package.Professional development and training opportunities.A chance to shape the future of Intas B2B’s operations.
