Director, Quality AssuranceLocation: Greater Greenville, SC Area
Some relocation support offeredLead enterprise-wide quality operations for my client in a highly regulated cGMP manufacturing environment. This is a high-impact leadership role driving compliance, continuous improvement, and product quality while building a culture of excellence.Why You Should ApplyLead Quality Assurance, QC Inspection, and Document ControlInfluence company-wide quality strategy and complianceDrive modernization of electronic Quality Management SystemsBuild and mentor a high-performing quality teamWhat You’ll Be DoingLead QA/QC operations, document control, CAPA, deviations, audits, and change controlOversee material and finished goods release and batch certificationEnsure compliance with cGMP, FDA, OSHA, and regulatory requirementsDirect internal/external audits, supplier quality, investigations, and trainingChampion continuous improvement and cross-functional quality initiativesAbout YouBachelor's degree in a related fieldExperience leading QA within a cGMP manufacturing environmentStrong knowledge of CAPA, change control, document control, audits, and quality systemsProven leadership, coaching, and talent development skillsExcellent problem-solving, regulatory, and cross-functional communication abilitiesHow To ApplyWe’d love to see your resume, but we don’t need it to have a conversation. Send us an email to and tell me why you’re interested. Or, feel free to email your resume. Please include Job#20006.#LI-MP1Type: ContractCategory: Pharmaceutical ManufacturingDate Posted:
Some relocation support offeredLead enterprise-wide quality operations for my client in a highly regulated cGMP manufacturing environment. This is a high-impact leadership role driving compliance, continuous improvement, and product quality while building a culture of excellence.Why You Should ApplyLead Quality Assurance, QC Inspection, and Document ControlInfluence company-wide quality strategy and complianceDrive modernization of electronic Quality Management SystemsBuild and mentor a high-performing quality teamWhat You’ll Be DoingLead QA/QC operations, document control, CAPA, deviations, audits, and change controlOversee material and finished goods release and batch certificationEnsure compliance with cGMP, FDA, OSHA, and regulatory requirementsDirect internal/external audits, supplier quality, investigations, and trainingChampion continuous improvement and cross-functional quality initiativesAbout YouBachelor's degree in a related fieldExperience leading QA within a cGMP manufacturing environmentStrong knowledge of CAPA, change control, document control, audits, and quality systemsProven leadership, coaching, and talent development skillsExcellent problem-solving, regulatory, and cross-functional communication abilitiesHow To ApplyWe’d love to see your resume, but we don’t need it to have a conversation. Send us an email to and tell me why you’re interested. Or, feel free to email your resume. Please include Job#20006.#LI-MP1Type: ContractCategory: Pharmaceutical ManufacturingDate Posted:
Director Quality in greenville at Unknown Company
This position is listed as contract and onsite.