Planet Technology

Lab Empower Quality Control & Validation Specialist – (Onsite) – Contract – Northeastern Ohio. Biotechnology Research organization seeks a Lab Empower QC & Validation Specialist for an onsite 7-month contract.. This requires 4+ years method development and validation expertise with HPLC/UPLC, and GC. Ideal candidate will also have 4+ years in analytical chemistry, with method validation and Waters HPLC expertise, having utilized Empower specifically.. + years of method development, validation expertise with HPLC/UPLC, and GC.. years analytical chemistry method validation, ideally having utilized Waters HPLC.

validation specialist

Lab Empower Quality Control & Validation Specialist – (Onsite) – Contract – Northeastern OhioBiotechnology Research organization seeks a Lab Empower QC & Validation Specialist for an onsite 7-month contract. This requires 4+ years method development and validation expertise with HPLC/UPLC, and GC. Ideal candidate will also have 4+ years in analytical chemistry, with method validation and Waters HPLC expertise, having utilized Empower specifically. Prior Training within ISO 9001 and cGMP is also required. This opportunity requires proficiency in chromatography techniques to include gas chromatography and high-performance liquid chromatography. No 3rd parties please, and please ensure you possess all requirements if you are to apply for this position. Opportunity offers somewhat long-term contract with possible extensions. Requirements: <ul><li>bachelor’s degree in Chemistry, Biology or Biochemistry.</li><li>or Green Card holder local to northeastern Ohio.</li><li>+ years of method development, validation expertise with HPLC/UPLC, and GC.</li><li>years analytical chemistry method validation, ideally having utilized Waters HPLC.</li><li>with Empower and Microsoft Office Suite (Word, Excel and Access).</li><li>and cGMP training and experience.</li><li>with chromatography techniques to include both gas and liquid.</li><li>in deviation and complaint investigations to include root cause analysis and technical writing.</li></ul> Responsibilities: <ul><li>method development, verification, and validation through the utilization of advanced analytical instruments to include UHPLC (RI, CAD, PDA); GC (FID/TCD).</li><li>of all regulatory standards within a Quality Control Laboratory to include cGMPs, cGLPs, ISO 9001 and other safety regulatory standards.</li><li>with internal departments to achieve project and organizational goals.</li><li>in handling projects within scientific and ethical quality standards.</li><li>laboratories are safely and securely operating regarding personnel, equipment and site protection.</li><li>deviation and complaint investigations to include root cause analysis and technical writing.</li></ul> Benefits: A 7-month contract within a stable and successful organization with the potential to extend.

START NEW SEARCH