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, while providing a particularly strong expertise in Liquids, Ointments and Creams.
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 of the Chemical Laboratory area 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 AuditsEducation: Degree in Chemistry, Pharmacy or Related SciencesProfessional Experience: Minimum experience of 3 years in Pharmaceutical IndustryExcellent organizational and planning skillsOrder and precision in the execution of activitiesRespect, transparency and good communication skillsAbility to work in a teamSeniority levelAssociate
Employment typeFull-time
Job functionQuality Assurance
IndustriesPharmaceutical Manufacturing
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