Product Development Scientist (12 month contract)

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2019, Eurofins generated total revenues of EUR 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years. We are currently recruiting for an enthusiastic and innovative Product Devlelopment Scientist for a 12 month full time temporary position to be based at our client's facility, a world class Pharmaceutical company based in Macclesfield. We have opportunities for experienced Analytical Scientists with at least 2 years' experience of product development in the pharmaceutical industry. The purpose of this job is to provide analytical support on drug product development projects. The role will involve liaising with both internal clients and external collaborators and duties may include providing direct analytical support, developing and validating analytical methods and working on tech transfers. The ideal candidate will have strong technical skills, report writing skills, problem solving skills, to be able to think logically and have the ability to effectively collaborate with and communicate scientific ideas to both internal and external partners is a requirement. There are excellent career progression paths and opportunities to expand knowledge and expertise within the role. Job Description At least 2 years' experience in the analytical pharmaceutical industry. Technical Transfer experience is essential Knowledge and experience within a pharmaceutical product development environment and an understanding of the drug development process would be desirable. Method Development and Method Validation experience. Knowledge and experience in the use of techniques such as HPLC and GC within a development environment is essential. At least 2 years' relevant experience of pharmaceutical analysis in a development laboratory. Stability experience would be an advantage. Good understanding of requirements for working in a GMP environment. Ability to quickly learn new processes. Ability to work using fully electronic media, including MS Office. Ability to communicate clearly and to form strong working relationships with colleagues. Ability to work on own initiative and be capable of developing solutions to problems as part of a team. Willing to operate in a flexible manner and be able to switch priorities at short notice. Good team player, organised, accurate, have strong documentation skills. Passionate about quality and customer service. Enjoys the challenges of working in a fast paced and changing environment. Ability to prioritise, manage time and handle a diverse workload. Qualifications BSc in science and/or masters in a relevant field with a strong emphasis on analytical science Additional Information * Method Validation experience required. * A sound, fundamental knowledge of Chemistry is essential. * Good foundation and experience with traditional analytical techniques as well as modern instrumental equipment (HPLC, UPLC, MS, vibrational spectroscopy, dissolution, Karl Fischer, and UV spectroscopy). * Ideally experience in the use of Empower CDS and operating with fully electronic media. * Must possess strong knowledge of analysis methods and tools. * Appropriate relevant experience of pharmaceutical analysis in a development laboratory within a group organization. * Good Team player. * Collaborative communication skills. Additional Information Initial contract term 12 months with a view to extension beyond. Qualifications: BSc in science and/or masters in a relevant field with a strong emphasis on analytical science Additional Information Method Validation experience required