PpWith its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. /ppWe are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries. /ppAt Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves. /ppThis drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases. /ppRecordati. Unlocking the full potential of life. /ph3Job Purpose /h3pWe are seeking a Quality Assurance Specialist to work together to ensure the high quality of our operations and services, with the goal of ensuring the long-term success of our business. Your duties include inspecting procedures and products, identifying errors or nonconformity issues in products and related manufacturing processes and analysis. /ppEstablish quality and safety standards and criteria to be met. /ppEstablish procedures for monitoring achievement of standards. /ppAnalyze and supervise business processes from production to marketing of products and draft related documentation. /ph3Key Responsibilities /h3ulliBatch record review /liliProduct quality review /liliSupplier qualifications /liliProcess validations /liliSOPs revision /liliMonitoring and tracking closure and timelines of quality system KPI’s (including deviation, change control and CAPA) /liliOther quality system related tasks /li /ulh3Required Education /h3pBachelor's degree in a scientific discipline /ph3Required Skills And Experience /h3ulliExperience of 2+ years working as a Quality Assurance Specialist or other similar position in a GMP regulated pharmaceutical environment or equivalent. /liliSignificant experience using quality assurance methodologies and standards and managing GMP documents and version control. /liliSignificant experience in data analysis and statistical methods /liliGood hands-on experience with MS Office and databases /liliStrong numerical skills, great attention to detail, and a results-oriented approach /liliStrong communication, organizational and leadership skills /liliStrong ability to work on own initiative or in a cross-functional team. /liliQuality control certification, such as ISO 9000, will be a bonus. /li /ulh3Required Languages /h3pEnglish fluent /ppAt Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential. /ppWe are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief. /ppIf you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today. /p /p #J-18808-Ljbffr