Pharma Manufacturing QA

1,567 open positions

QA Manager PeopleservicesID Jakarta 2y Managing product quality, compliance, and regulatory reporting for pharmaceutical products.
Senior Business Consultant - Life Sciences Quality VeevaRemote $80k2y Lead consulting programs to transform Life Sciences operating models, driving organizational change and delivering safe, effective products via Quality, Manufacturing, and Supply Chain improvements.
Associate Manager/ Manager, Quality Assurance PeopleservicesSG Singapore 3y Establishing, implementing, and maintaining a Quality Management System for pharmaceutical products in compliance with GxP (GDP, GMP) and regulatory standards.
Lead Auditor- Healthcare EurofinsGujrat, PB, in 3y Conduct supplier audits for pharmaceutical, medical device, and cosmetic companies to ensure compliance with regulatory standards and quality management systems.
Standortleiter Quality / Compliance Marburg (m/w/d) PPT Pharma Process Technology GmbHMarburg, HESSEN 4y Leading Quality and Compliance operations for pharmaceutical clients, ensuring adherence to GMP, FDA, and ICH standards across project lifecycles.
Sachkundige Person / Qualified Person (m/w/d) Pharma Rottendorf Pharma GmbHRemote 4y Responsible for releasing manufactured pharmaceutical products in compliance with legal requirements (§ 14 AMG, Annex 16) and managing GMP documentation.
Technical Consultant - Quality Systems VeevaRemote 12000k–23000k4y Technical consultant implementing and configuring Veeva Quality applications for life sciences companies to ensure regulatory compliance and operational efficiency.
Senior Technical Consultant - Quality Systems VeevaRemote 18000k–33000k4y Implement and support Veeva Quality suite solutions for life sciences companies to enhance quality, compliance, and audit readiness.
QA/QC Manager (m/w/d) Cannamedical Pharma GmbHKöln 5y Quality Manager responsible for optimizing systems, managing deviations, complaints, change control, SOPs, and management reviews in a highly regulated pharmaceutical environment.
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Job QA Operations Scientist ensuring GMP compliance, operational readiness, and quality standards in pharmaceutical manufacturing.
About the job SK Group경상북도 안동시 Operate QA systems for deviation and change control, ensure data integrity, and manage GMP upgrade projects in a pharmaceutical manufacturing environment.
About the job SK Group인천 송도 Ensuring GLP/GCLP/GMP compliance for R&D data, experiment records, and reports; managing SOPs and data integrity.
About the job SK Group및 기타사항 Support GMP raw material supplier qualification, change control, quality audits, risk assessments, and compliance reviews for a pharmaceutical contract manufacturing organization (CMO).
About the job SK Group경기도 판교 Establishing and operating a Quality Assurance (QA) system to ensure data integrity, compliance with GxP regulations, and product quality throughout drug development and commercialization.
About the job SK Group경북 안동 Operating GMP quality systems, managing quality documents, reviewing manufacturing/testing records, and handling deviations, change controls, CAPA, validation, and qualification activities.
About the job SK GroupSK플라즈마 안동분획센터 Operating Quality Management Systems (Change Control, Lab Investigation) and Document Management Systems (Batch Record, Master Formula) at a plasma fractionation center.
Director/Senior Director of Asset Quality Assurance TrialSparkBoston / New York $178k–$307k Designing quality frameworks and embedding Quality by Design (QbD) principles into drug development programs to accelerate assets from preclinical to commercial phases.

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