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-Spectrophotometer Extensive experience in a cGMP environment in reviewing analytical documentation and knowledge of related issues concerning DI Good understanding of regulatory practices and standards Responsible 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 standards Ensure that all activities conducted comply with SOPs and cGMP regulatory standards Stability testing on finished products and intermediates Review of analytical data in accordance with procedures Knowledge of company procedures and GMP Familiarity with laboratory computerized programs and management software Collaborate with cross-functional teams to achieve company goals Maintain accurate and complete records of activities performed Strictly follow protocols and procedures to ensure compliance with regulatory and company standards Determine and implement improvements to optimize workflows and processes Participate in calls with clients for updates on activities and project status Collaborate in conducting Internal and External Audits Education: Degree in Chemistry, Pharmacy or Related Sciences Professional Experience: Minimum experience of 3 years in Pharmaceutical Industry Excellent organizational and planning skills Order and precision in the execution of activities Respect, transparency and good communication skills Ability to work in a team Seniority level Associate Employment type Full-time Job function Quality Assurance Industries Pharmaceutical Manufacturing J-18808-Ljbffr