Aviva Natural Supplements is a GMP & USDA Organic turnkey contract manufacturer located in New Brunswick, NJ. Specializing in custom formulation, blending, encapsulations, compression and high-speed packaging lines,
Role Description
This is a full-time on-site role for a SOP Document Control Specialist at Aviva Natural Supplements in New Brunswick, NJ. The Document Control Specialist will be responsible for managing, reviewing, and organizing various SOP documents and associated Forms, ensuring quality control, and overseeing document-related processes on a regular basis. The Specialist will report to the Senior Manager - Quality Assurance.
Qualifications
Documentation and Records Management skills
Document Review and Quality Control expertise
Experience in Document Management
Attention to detail and organizational skills
Knowledge of GMP and regulatory requirements
Strong communication and interpersonal abilities
Proficiency in MS Office and document control software
Previous experience in a manufacturing or pharmaceutical setting is a plus