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Join our team as an Analytical Excellence & Quotation Officer! About the role: The Analytical Excellence Lead is responsible of the implementation of state-of-art science and practice in analytical development, method validations and transfers. Key contributor of CDMO quotations’ analytical part. Main responsibilities: Analytical excellence Proposes and leads transversal strategic initiatives for analytical development allowing to build and maintain state-of-the-art competencies and techniques in analytical sciences. Supports local teams with scientific expertise to prevent problems and recommends solutions in analytical development Provides technical guidence, leadership and decision-making as appropriate in analytical development, method validations and transfers. Provides regular performance feedback, development and coaching to the network Defines report writing and storage policy for Analytical Development Supports teams related to Scientific Information retrieval projects Contributes to the transversal global network of analytical development experts within EUROAPI R&D Establishes and fosters relationships to academic partners, monitors and ensures progress of academic collaboration programs. Facilitates analytical transfer between organizations and sites to meet required project goals. CDMO quotations’ analytical part Contribute to CDMO opportunity screening, technical assessments, and cost estimates. Interact closely with project teams and customers across regions to support development choices and industrial feasibility. Participate to the work of the quotation team, makes technical evaluation of offers, participate to customer call to define offer details and customer visit management Write technical part of proposals, compile costing file and time schedule Align quotations with Business Development and Industrial Operations Requirements: Education in Biology, Biotechnology, Chemical Engineering, Chemistry, or equivalent education. Ph.D. being a plus At least 10 years of experience in analytical development related to developing and filing APIs. Experience in GMP practice of analytical development, transfers and quality control. Highly skilled expert with proven track record in analytical development CMC for Active Pharmaceutical Ingredients including GMP knowledge Experience with document management systems Good knowledge of MS Office tools (Outlook, PowerPoint, Excel, Windows) Languages: Strong verbal and written communication skills in English French is a plus Major competences and skills: Ability to effectively communicate across the organization at all levels. Strong organizational, inetrpersonal and decision-making skills Strong personal initiative, global team leadership, managing across cultures, participation and change management, working through others, multitasking in complex environment, and risk taking Why join us? According to the company's Cafeteria policy, gross 636,000 HUF/year (also during the probationary period) Free outpatient healthcare services and specialist consultations at Buda Health Center, plus the opportunity to participate in an annual preventive health screening, with a paid day off granted for the appointment Discounted sports and wellness opportunities: AYCM membership, on-site fitness center and sauna, as well as discounted access to sports facilities Collective life and accident insurance Voluntary pension fund membership (supplemented with employer contribution) Free parking Commuting and weekend travel reimbursement For employees based in Budapest, a fixed monthly commuting allowance Annual performance bonus, referral bonus, and service anniversary bonus 14 weeks of paid parental leave for new parents Free online language learning through the goFLUENT platform Company events and community programs, such as Family Day and seasonal celebrations including St. Nicholas Day and Christmas events Coffee and snack card, redeemable at on-site vending machines A variety of one-time employee support benefits, including contributions toward prescription glasses and home office equipment. EUROAPI is a leading supplier of active pharmaceutical ingredients (APIs), spun out from Sanofi on May 6, 2022 and listed on EURONEXT, with the aim of becoming a global champion in API solutions and CDMO. The company has a diversified portfolio of approximately 200 APIs for its API Solutions business and its CDMO (Contract Development and Manufacturing Organization) activities. With more than 150 years of experience in the API market, around 3,350 employees and a consolidated turnover of approximately €1 billion in 2023, EUROAPI has six production sites and development centers equipped with state-of-the-art technology, all located in Europe (France, Germany, Hungary, Italy and the UK). Euroapi is focused on reinventing active pharmaceutical ingredients to sustainably meet customers’ and patients’ needs around the world. We are a leading player with approximately 200 products in our portfolio, offering a large span of technologies while also developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities. With strong R&D capabilities and five manufacturing sites located in Europe, Euroapi provides its clients with high-quality API solutions in more than 80 countries. Our 3000+ people are committed to building together the future of public health by advancing and securing access to essential active ingredients, at the core of the healthcare value chain. Find out more at www.euroapi.com 
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euroapi
Budapest
Analytical Excellence & Quotation Officer.
more at euroapi.
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