Analista del controllo qualità senior

Varese 18-09-2025

Analista del controllo qualità senior

JR Italy Varese 18-09-2025
Riassunto

Località

Varese

Divisione Aziendale

Tipo di contratto

Data di pubblicazione

18-09-2025

Descrizione Lavoro

Social network you want to login/join with:col-narrow-leftClient:FAMARLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:356155221660925952033712Job Views:3Posted:27.08.2025Expiry Date:11.10.2025col-wideJob Description: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 toStandard Operating Procedures (SOPs)Optimization of analytical methods; Transfer and validation of methods.Preparation of protocols and reports concerning transfer and analytical validation activities inaccordance 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 optimise workflows and processesParticipate in calls with clients for updates on activities and project statusCollaborate in conducting Internal and External AuditsEducation: Degree in Chemistry, Pharmacy or Related SciencesProfessional Experience: Minimum experience of 3 years in the Pharmaceutical IndustryExcellent organizational and planning skillsOrder and precision in the execution of activitiesRespect, transparency and good communication skills
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