Quality Compliance & Regulatory Affairs Lead
JAK Diversified II INC
Truvant Health and Beauty seeks a QA Compliance & Regulatory Affairs Manager to lead the QMS and ensure FDA/cGMP and customer standards compliance. Responsibilities include deviations, CAPAs, change controls, audits, document control, training, supplier qualification, and continuous improvement initiatives. The role oversees QA systems and QA training to ensure documentation practices, training programs, and compliance records are maintained, supporting new client onboarding, product launches, #J-18808-Ljbffr JAK Diversified II INC
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...yourself and have never been afraid of putting in the hard work it takes to achieve them; Confidence and Presence: You enjoy taking the lead and inspiring others with your passion and commitment; Passion for Content: You relish literature, science, history, and/or math...SuggestedFull timeTemporary workSummer holidayWork at officeVisa sponsorship- ...Corporate & External Affairs Analyst Lead About the role: As an Corporate & External Affairs... ...support for governance and entity compliance matters across all regulated corporate... ...Liaise with corporate governance, regulatory legal, risk, compliance, internal audit...RegulatoryWork experience placementWork at officeFlexible hours
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...Description Visa is seeking a lawyer to join its growing Global Regulatory Affairs team. The position will report to the Vice President, Global... ...priorities, consistently deliver exceptionally high-quality work product, and meet tight deadlines. Work Hours: Varies...RegulatoryFull timeWork experience placementWork at officeLocal areaWork visa$114.1k - $268.18k
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$105k - $115k
External Affairs Lead Remote About AiEDU The AI Education Project (aiEDU) is a growing 501(c)(3) non-profit that creates equitable educational... ..., compensation, eligibility for benefits and termination. In compliance with federal law, all persons hired will be required to...Full timeTemporary workLive inLocal areaImmediate startRemote workHome officeFlexible hours- ...job poster from Medasource Regulatory Compliance Specialist - EU Clinical Trials... ...) Overview Our client, a leading pharmaceutical company, is seeking... ...to support a high-impact Quality Management System (QMS)... ...compliance—not just regulatory affairs—and be ready to make an immediate...RegulatoryFull timeContract workImmediate startRemote work
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