Position: GMP Analyst Responsibilities: Conduct GMP analysis. Manage a designated area in the QC department, ensuring adherence to procedures related to Quality, Environment, and Safety. Raise and investigate deviations and out-of-specifications within QC. Promote and develop continuous process improvements, including method development and process evolution. Write protocols, reports, and SOPs. Learn and understand the management system of Quality. Learn tools and procedures applied within the site. Support laboratory activities related to the development and validation of analytical processes. Requirements: Experience in Quality Control within the Chemical-Pharma industry. Knowledge and proper use of QC devices: GC (Injection and Head-space), HPLC, spectrophotometers, atomic absorption/ICP-MS. Ability to manage data flow, deviations, and OOX. Good knowledge of GMP and ISO standards. Familiarity with AIFA and FDA audits. Proficiency in English (reading and speaking). Availability to work in shifts. What We Offer: Temporary contract with an external agency until December 2025. Free access to the company canteen. Benefits supporting physical, financial, social, and mental wellbeing, including gym access, psychologist, volunteering, parental benefits, and more. Opportunities for professional and personal development through various programs, including language learning and professional courses. At Boehringer Ingelheim, we are committed to equal opportunities, fostering a work environment based on respect, trust, and empathy, free from discrimination. We value diversity and inclusion, believing our differences are our strengths. #J-18808-Ljbffr