Jobs at Genovice INC

Leads quality-system development and computerized system validation governance for a regulated technology company. Responsibilities include building the QMS, authoring SOPs, overseeing document and change controls, CAPA, deviations, training, supplier quality, audits, validation reviews, data-integrity controls, inspection readiness, and regulated product-release approvals. The role provides independent Quality oversight rather than executing routine testing and requires approximately 20 hours per week.

Develops, revises, formats, and reviews GMP master batch records and manufacturing documentation. Collaborates with Quality, Manufacturing, and technical experts to gather information, ensure compliance with GMP and site procedures, manage document revisions and approvals, maintain version control, identify documentation gaps, and support corrections. Requires pharmaceutical or life-sciences batch-record experience, technical writing and editing skills, and familiarity with document-control or electronic quality-management systems.