This position would provide support and remediation for all chemistry-related projects for the products on the market. In addition, the position would also provide assistance in the validation of new manufacturing processes and conduct stability testing analysis required for approval of these processes What is expected of you for success in your role o Demonstrates developed knowledge of respective scientific discipline and standard scientific method and techniques o Understanding of GMP documentation requirements o Excellent scientific writing skills o Ability to multi-task various activities. o Ability to work in a team and dynamic environment. o Troubleshoot issues that arise and solve problems o Ability to discuss scientific strategies/results and interact with other functional areas, including Regulatory, Manufacturing, and Quality. Qualifications o Education: BS in Chemistry / Pharmaceutics with related science experience o Experience: 2-4 years experience in pharmaceutical analytical chemistry is essential o Work within an FDA regulated environment o Experience with GMP documentation requirements o Hands-on experience with wet-chemistry testing techniques (i.e. pH, GC, HPLC) o Previous experience with writing scientific protocols and reports o Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
Associated topics: biochemistry, ceramic, chemistry, coating, formulation, glass, latex, material, material science, rubber
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