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Senior Quality Control Analyst
FAMAR
Milano
In loco
EUR 30.000 - 45.000
Tempo pieno
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Descrizione del lavoro
Une entreprise de fabrication et de développement dans l'industrie pharmaceutique recherche un Scientifique en Contrôle de Qualité pour son laboratoire à Milano. Le candidat jouera un rôle essentiel dans les analyses, la validation des méthodes, et veillera à la conformité avec les normes de qualité. Ce poste est idéal pour un professionnel ayant au moins 5 ans d'expérience dans l'industrie et un diplôme pertinent.
Competenze
- Minimum 5 ans d'expérience dans l'industrie pharmaceutique.
- Expérience en validation des méthodes analytiques.
- Capacité à travailler en équipe et excellente organisation.
Mansioni
- Effectuer des analyses en conformité avec les SOPs et les normes cGMP.
- Optimiser les méthodes analytiques et préparer les rapports.
- Collaborer avec des équipes pluridisciplinaires pour atteindre les objectifs de l'entreprise.
Conoscenze
Formazione
Strumenti
Descrizione del lavoro
FAMAR is a European contract manufacturing and development partner for the pharmaceutical and health & beauty industry. Building on our 70 years’ expertise, we deliver flexible solutions, from development to production and distribution. Driven by our customer-care mindset, we offer services covering the majority of pharmaceutical forms. Through the outstanding knowledge and commitment of our 1850 employees and with a network of 6 production sites, we supply a wide range of 1800 products in 125 international markets. For the Italian plant in Baranzate specialising in the production of oral solids, we are currently looking for a Quality Control Scientist to join the Quality Control Laboratory. In this role, you will play a crucial role in carrying out the analytical activities in full compliance with the company's times, procedures and standards of production efficiency and quality.Skills & Responsibilities : High proficiency in analytical instrumentation for the analysis of small and large molecules, particularly with the use of HPLC, GC, IR, UV-SpectrophotometerExtensive experience in a cGMP environment in reviewing analytical documentation and knowledge of related issues concerning DIGood understanding of regulatory practices and standardsResponsible for testing raw materials, in-process products, and finished products according to Standard Operating Procedures (SOPs)Optimization of analytical methods; Transfer and validation of methods.Preparation of protocols and reports concerning transfer and analytical validation activities in accordance with Company and International standardsEnsure that all activities conducted comply with SOPs and cGMP regulatory standardsStability testing on finished products and intermediatesReview of analytical data in accordance with proceduresKnowledge of company procedures and GMPFamiliarity with laboratory computerized programs and management softwareCollaborate with cross-functional teams to achieve company goalsMaintain accurate and complete records of activities performedStrictly follow protocols and procedures to ensure compliance with regulatory and company standardsDetermine and implement improvements to optimize workflows and processesParticipate in calls with clients for updates on activities and project statusCollaborate in conducting Internal and External AuditsBackground & Soft Skills : Education : Degree in Pharmaceutical Sciences, Chemistry, Pharmacy or Related SciencesProfessional Experience : Minimum experience of 5 years in Pharmaceutical IndustryStrong experience in analytical validation activities and methodsExcellent organizational and planning skills Order and precision in the execution of activitiesRespect, transparency and good communication skillsAbility to work in a team
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