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Document Control Specialist

USA - New York - Oak Hill💼 Full-time🗓 2026-09-28

Core

Manage document control applications and quality system activities to ensure product and process compliance with regulatory agencies and company standards.

Role type

Document Control Specialist (Quality Systems)

Builds

Quality systems, controlled documentation, and electronic tracking systems for consumer health products.

Domain

Consumer health / Pharmaceuticals / GMP

Required skills

Document control application administration, GMP compliance, quality review and approval, document lifecycle management, contingency planning, audit support, continuous improvement, cGMP knowledge

Preferred skills

None stated

Technologies

Document Control Application, electronic tracking systems

Responsibilities

Act as Local Business Administrator for the Document Control Application; deploy or enhance the network application; participate in DCA network meetings; review and approve GMP documents; support document authors and approvers; manage contingency plans; support audit and inspection processes; implement continuous improvement opportunities.

Seniority

Mid-level, hands-on IC

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