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Senior Analytical QC Chemist - 0QK3880289
Senior Analytical QC Chemist - 0QK3880289-March 2024
Fishers
Mar 31, 2026
About Senior Analytical QC Chemist - 0QK3880289

  Who We Are

  Ott Scientific

  The Ott Scientific family of companies comprises Polysciences, Bangs Laboratories, and Ethos Biosciences. Together, we bring the whole of our experience with best-in-class facilities and scientific, technical, analytical, and manufacturing capabilities to serve customers around the globe. We deliver highly specialized products and services that support scientific discovery and innovations.

  Bangs Laboratories

  Bangs Laboratories experience in microsphere synthesis and fine particle analysis have established us as a leading manufacturer of polymer, silica and magnetic microspheres for diagnostic, research, and flow cytometry applications. We also manufacture many specialty products to support validation and QC programs for analytical instruments, including a broad portfolio of fluorescent, count, size, and cell viability standards

  Bangs Laboratories is looking for a Senior Analytical QC Chemist. This role will conduct routine analyses independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. Must have the ability to work collaboratively, multitask and adapt to changing priorities and timelines.

  Demonstrate ability to qualify on basic QC instrumentation, skills related to general laboratory techniques, and GMP-related documentation.Perform wet chemical and instrumental analyses of raw materials, intermediates, and final product.Help with maintaining and troubleshooting analytical instrumentation. Order spare parts and essential items in a timely manner. Manage instrument contracts and annual calibration.On a regular basis perform calibration and validation of instruments.Prepare method validation and/or method transfer documentation.Contribute to a cohesive team environment and maintain a positive attitude.Understand data generated, and history of methods.Identifies problems, determine appropriate actions, and implement solutions with support or independently as appropriate.Applies GMP/ISO13485:2016 in all areas, as appropriate.Able to adapt to new procedures or needs as directed.Able to identify critical steps in an assay.Lead detailed investigations, product impact assessments, root cause determinations and implementation of corrective action.Perform stability testing and manage overall program.Maintain master equipment list and determine all PMs and calibrations.Supervise the work of QC Scientists/TechsEqual Opportunity Employer - minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity

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