Requirements: English
Company: Recordati Group
Region: Correggio , Emilia-Romagna
Join to apply for the Quality Assurance Specialist role at Recordati.With 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.We 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.At Recordati, our mantra is simple. Weve 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.Job PurposeWe 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.Key ResponsibilitiesBatch record reviewProduct quality reviewSupplier qualificationsProcess validationsSOPs revisionMonitoring and tracking closure and timelines of quality system KPIs (including deviation, change control and CAPA)Other quality system related tasksRequired EducationBachelor''s degree in a scientific discipline.Required Skills And ExperienceExperience of 2+ years working as a Quality Assurance Specialist or other similar position in a GMP regulated pharmaceutical environment or equivalent.Significant experience using quality assurance methodologies and standards and managing GMP documents and version control.Significant experience in data analysis and statistical methods.Good hands-on experience with MS Office and databases.Strong numerical skills, great attention to detail, and a results-oriented approach.Strong communication, organizational and leadership skills.Strong ability to work on own initiative or in a cross-functional team.Quality control certification, such as ISO 9000, will be a bonus.Required LanguagesEnglish fluent.At 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.We 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.If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.Seniority levelEntry levelEmployment typeFull-timeJob functionQuality AssurancePharmaceutical Manufacturing#J-18808-Ljbffr