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Detalii loc de munca - Anglia

Descrierea jobului - Anglia

Req ID: R0011049 Novex Pharma Limited is the leading global pharmaceuticals company focused on serving people with rare diseases and other highly specialized conditions. We strive to develop best-in-class products, many of which are available in more than 100 countries, across core therapeutic areas including Hematology, Immunology, Neuroscience, Ophthalmic, Lysosomal Storage Disorders, Gastrointestinal/Internal Medicine/Endocrine and Hereditary Angioedema; and a growing franchise in Oncology. Our employees come to work every day with a shared mission: to develop and deliver breakthrough therapies for the hundreds of millions of people in the world affected by rare diseases and other high-need conditions, and who lack effective therapies to live their lives to the fullest.

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Primary Duties The primary role is to support the analytical sample testing and documentation of results for process development. He/She will be responsible for preparing buffers, managing reagent inventory, maintaining instrumentation and executing experimental procedures and reporting data in a timely manner. He/She will be a contributor in the method qualification and transfer as needed, reviewing protocols, reports as needed. Responsibilities 80%: Execution of existing Test Methods 10%: Documentation of results 10%: Troubleshooting, control trending, assay transfer and qualification support as needed Education and Experience Requirements BS with 2-4 years or MS with 1-2 years’ experience in Analytical, Chemistry, Biochemistry or other biological discipline. Experience in biotechnology, pharmaceutical, or related environment. Skilled in the application of one or more technical skills. Experience in method transfers, assay qualification is a plus Key Skills, Abilities, and Competencies Proficiency in diverse analytical techniques like HPLC, DNA, Electrophoresis is required along with basic biochemistry laboratory techniques Computer competency is essential with emphasis on spreadsheet-based software. Accurate documentation and communication skills Ability to adhere to strict cnGMP procedures when applicable is required Strong analytical and problem solving skills Ability to report issues as needed Ability to work in a team Complexity and Problem Solving Solves routine problems of limited scope and complexity. Operates under compliance requirements and systematically seeks guidance on policies and practices Documents data accurately and completely as per established company guidelines and SOPs. Will be able to work independently with some supervision.

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