Senior QC Analyst - Method Development & Validation

There couldn't be a better time to join EUROAPI UK, a Sanofi company. Our vision is to reinvent active ingredient solutions to sustainably meet customers and patients' needs around the world. The Opportunity QC at EUROAPI UK manages commercial testing, UK importation testing and release, method validation and verification, analytical transfers and microbiological testing . You will join a team of QC Analysts, Micro QC Analysts and Senior Analysts led by a QC Team Lead to work on some exciting projects as we develop our Contract Manufacturing and Development business. Your role will be pivotal to how we develop our existing service offering - your purpose will be to strengthen our technical expertise in method development and validation. You will: Lead on analytical method development and validation projects for QC Manage multiple method validation projects to completion Perform analytical work in support of method development and validation projects that cover product process improvements, new products and equipment introductions Develop expertise within the team in the analytical method validation process The Company EUROAPI is a new player in Active Pharmaceutical Ingredients (API) created within Sanofi with the purpose of becoming an autonomous company in 2022. EUROAPI will combine Sanofi's API commercial and development activities with six of its European API production sites located in Brindisi (Italy), Frankfurt Chemistry (Germany), Haverhill (UK), St Aubin les Elbeuf (France), Újpest (Hungary) and Vertolaye (France). By operating autonomously, EUROAPI will have a broad portfolio of volume and niche products and will leverage an extensive commercial network covering more than 80 countries. With approximately 3200 employees and €1 billion in expected sales by 2022, EUROAPI plans to become the leading European Active Pharmaceutical Ingredients company. We are looking for A chemistry degree Analytical validation, analytical development and method development expertise gained on projects in a GMP setting Proven experience writing method validation protocols and using analytical equipment: HPLC, GC, KF, PXRD, DSC Experience in a regulatory enviroment working to tight timelines, experience in a CMO or CDMO would be preferred What we can offer you An excellent benefits package: we include an annual bonus, we pay 10% of your base salary into your pension annually with no contribution from you. We will give you free private medical insurance, personal dental cover, life assurance and income protection. You will also get access to our Boost rewards and discount scheme provided by Reward Gateway offering the best options to make savings on everyday purchases. We can offer a great site with unlimited hot drinks via our coffee machines and a subsidized canteen offering fresh sandwiches and cooked food for as little as £2.00. You can learn beekeeping with our beekeepers onsite, join one of our employee-led groups for animal lovers, wellbeing, exercise classes and much more. Commuting to Haverhill is easy, we offer onsite parking and a location free from inner city traffic. We occupy an advantageous position on the borders of Cambridgeshire, Essex and Suffolk, right at the heart of the East of England. Visas for those who do not already have the right to work in the UK will be considered on a case-by-case basis according to business needs and resources.

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