The Position For our site in Fornovo San Giovanni (BG) we are looking for a CMC Scientific Writer to join our Drug Regulatory Affairs team responsible for the preparation of CMC (Chemistry, Manufacturing and Control) documentation Tasks & Responsibilities Tasks & Responsibilities: • In-time preparation, compilation and maintenance of CMC documentation for global submissions based on international pharmaceutical requirements, aligned with the corresponding GxP relevant documentation • Writing the required CMC documentation in close collaboration with co-authors or subject matter experts at the respective manufacturing sites • Coordinating the review and approval cycles for all relevant CMC submission documents among the relevant interfaces within the BI system to ensure regulatory compliance as well as legal and internal requirements • Providing further submission documentation including scientific documents (e.g. statements, justifications, etc.), DMF/CEP documentation for the drug substance in scope and contributes to responses to Health Authority questions on request • In addition, he/she supports the manager in assessing and defining the regulatory impact of internal change requests, manufacturing deviations and risk assessments Requirements • At least 2-3 years experienced in Regulatory Affairs or Quality Assurance; skill/experience gained in a similar position • Bachelor’s degree in Chemistry, Pharmaceutic or Biochemistry • Experience of working in a GMP environment • Native level of Italian language and B2 level of English • Ability to achieve and maintain high standards with meticulous attention to detail • Ability to work accurately in a busy and demanding environment, adhering to strict deadlines/timescales • Teamwork, problem solving and ability to work under pressure What we offer • For this position we offer a temporary, 1 year contract with an external agency • Free access to the company canteen and ticket restaurants when working remotely according to BI policy • A range of benefits for your physical, financial, social and mental wellbeing (access to gyms, psychologist, volunteering, parental support, company welfare and more) • A support to develop your own professional and personal path that will guide you through our full range of development programs including platforms to learn foreign languages and attend professional courses In Boehringer Ingelheim we are committed to guarantee equal opportunities; we believe in respect, trust and empathy, in a work environment without discrimination. We are powered by our people as we know that our differences are our strengths. We value everyone and each of us feels included, important and at ease. This job requisition is addressed also for candidates with disabilities and belonging to protect categories following articles 1 and 18, Law 68/99. All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.