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Nutrix · 23 hours ago

Quality Assistant Manager

Salt Lake City, UT

Full-time

Onsite

Entry, Mid Level

2+ years exp

Nutrix is a solutions-driven company specializing in contract manufacturing, private labeling, and product design. The Quality Assistant Manager is responsible for ensuring accuracy, compliance, and effective control of all quality-related documentation and processes within the organization.

CosmeticsManufacturingProduct Design

Responsibilities

Initiate, track, and close CAPAs; ensure root cause analysis, effectiveness checks, and timely resolution

Review and approve product and raw material specifications for accuracy, compliance, and alignment with customer requirements

Investigate, document, and complete complaint reports in accordance with internal procedures and regulatory guidelines

Review and approve or reject COAs to ensure accuracy, completeness, and compliance with specifications

Evaluate and approve deviations; ensure investigations, justifications, and corrective actions are properly documented

Review and approve change control requests, ensuring appropriate impact assessments, risk evaluations, and compliance with applicable regulations

Review, revise, and create SOPs in alignment with regulatory requirements and best practices; ensure proper formatting, control, and implementation

Assist with training activities related to SOPs, quality systems, and regulatory compliance; maintain training records and help drive training effectiveness

Qualification

Quality AssuranceRegulatory StandardsDocument ControlElectronic Document Management SystemsContinuous ImprovementAnalytical SkillsAttention to DetailOrganizational SkillsCommunication SkillsProblem-SolvingCollaborationIntegrity

Required

Bachelor's degree in Life Sciences, Quality, Regulatory, or a related field (or equivalent experience)

2+ years of experience in Quality Assurance, Quality Systems, or Document Control within regulated industries (cosmetics, pharmaceuticals, medical devices, or similar)

Strong understanding of regulatory standards (FDA, ISO 9001, ISO 22716, GMP)

Excellent attention to detail, organizational, and communication skills

Ability to manage multiple priorities and meet deadlines