QC Analyst Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards. You will achieve, together with your colleagues in Quality Assurance, Quality Control, Regulatory and Quality Systems, the delivery of a resilient supply of quality products to our clients. This opportunity is for a QC Analyst to join the QC Team for a 6 months contract with an immediate start, Your Responsibilities You will:

• Sample, analyze and release drug products and raw materials according to cGMP
• Work on the development and validation of analytical methods
• Calibration and qualification of laboratory equipment as stipulated in the appropriate procedures and recording of data.
• Drive compliance working with QA and promote quality standards.
• Archive internal laboratory documentation according to cGMP requirements related to laboratory analyses.

Our Company EUROAPI is focused on reinventing active ingredient solutions to sustainably meet customers’ and patients’ needs around the world. We are a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio, offering a large span of technologies, while developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities. Taking action for health by enabling access to essential therapies inspires our 3,450 people every day. With strong research and development capabilities and six manufacturing sites all located in Europe (Saint-Aubin-lès-Elbeuf and Vertolaye in France, Brindisi in Italy, Frankfurt in Germany, Budapest in Hungary and Haverhill in the UK), EUROAPI ensures API manufacturing of the highest quality to supply customers in more than 80 countries. EUROAPI is listed on Euronext Paris. The EUROAPI Italy facility is a vast production site with over 240 workers located in the industrial area of Brindisi with a history dating back to 1966. EUROAPI Italy is specialized in the development and manufacturing of Active Pharmaceutical Ingredients (APIs), including antibiotics, corticosteroids and other intermediates by large scale fermentation under GMP conditions. The Brindisi site is approved by the main health authorities and owns environment and workplace safety certifications. Our Requirements High school diploma as chemical/ Sciences degree Experiences in same fields Analytical chemistry methods GMP knowledge coupled with proven understanding of analytical method validation & transfer principles. Your Benefits

• Competitive Salary
• Annual Bonus
• Training & Development
• Shift work
• Company canteen

Culture & Values at EUROAPI We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognize that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right". Diversity & Inclusion EUROAPI is committed to nurturing a culture of diversity and inclusion that contributes to improving innovation, performance, and engagement. We value transparency, mutual respect, and equal treatment of people. For this reason, we are firm in protecting our employees against any forms of discrimination. Environment, Social and Governance We strongly believe that the success of our company lies in its capacity to adapt to tomorrow’s challenges. Our responsibility as a company is to provide sustainability and resilience to the pharmaceutical value chain. Apply Today! Find out more about this exciting opportunity, apply today!