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Posted: Thursday, June 22, 2017 7:25 AM

Beauty Manufacturing Solutions Corp. (BSMC) is a high:growth US contract manufacturer of beauty, baby care, and personal care products for top brands worldwide. The BMSC QC Analytical Chemist will be part of a team that is responsible for the successful production of materials and products that meet the high: quality standards set by management and clients. The Chemist will be responsible for conducting tests and evaluations of raw materials, bulk, and finished products by using organoleptic and instrumentation based test methods. This position is responsible for the operation and maintenance of method development for analytical instruments, including ICP:OES, HPLC and Mercury Analyzer. This position will work as part of a team that includes Quality Control, Quality Assurance and Regulatory. They will also work cross:functionally with Research and Innovation, Production and Manufacturing to ensure that specifications are being met. Additional duties include analyzing data, identification of unknown substances, trouble:shooting out of specification situations and assuring all customer and regulatory requirements are met. The position will report to the Quality Supervisor. BS/BA degree in Chemistry required5:10 years of experience in a GMP laboratory environment (cosmetic, OTC/personal care, food or pharmaceutical) requiredHPLC experience required. ICP:OES experience required, Heavy Metal analysis experience preferredCapability to develop HPLC and ICP analytical methods requiredStrong verbal and written communication skills expectedExperience troubleshooting, investigating and resolving analytical and inspection anomaliesFamiliarity with Corrective Action/Preventive Action strategies to drive continuous quality improvementDemonstrated knowledge of quality systemsExperience with internal and external audits a plusOrganized, analytical, self:directed, and motivatedCollaborative and team orientedMust be able to work flexible schedules including overtime and weekend shiftsShift assignment may change based on company needsMaintain and support Quality Standards : Ensure SOPs are followed to meet and exceed Quality Standards set forth in specifications and the requirements of FDA 21 CFR 21, Sections 210: 211, Good Manufacturing Practices.Maintain and support Safety : Ensure the team maintains the highest levels of safety and build an environment where the teamA?s wellbeing is top priorityPerform in:process and final inspections, measurements and analysis of bulk batches, finished goods, incoming components and/or raw materials in compliance with GMPs and all applicable regulations, standards and client requirements.Review data for compliance to specifications, reports and troubleshoots all non:conformances to specification or standardEnsure equipment is in calibration and performing as required; supplies and tools are available and in good conditionGenerate GMP compliant records as required SOP, method or regulationActively engage in continuous improvement of processes and proceduresProven ability to exercise judgment and appropriately escalate issues to Quality ManagementPerform all other duties as required by Quality managementRoles and Responsibilities will change to meet the growing needs of the company


• Location: North DFW

• Post ID: 57047353 northdfw is an interactive computer service that enables access by multiple users and should not be treated as the publisher or speaker of any information provided by another information content provider. © 2017