Analyst, Quality Systems (Two Openings)

Role: Quality Systems Analyst responsible for executing and supporting quality system activities within Johnson & Johnson's manufacturing environment. Objectives include managing document and data integrity, supporting audit and investigation processes, and driving process improvements. Responsibilities encompass site liaising, document lifecycle management, SOP updates, and project leadership, with occasional off-shift support. Requirements: bachelor’s degree in engineering, Science, or related field; minimum 2 years in QA/QC or quality systems; knowledge of cGMP regulations; strong communication, collaboration, and time management skills. Preferred: experience in a fast-paced manufacturing setting. High-value specifics: focus on cGxP compliance, document management, audit support, and risk identification in a regulated pharmaceutical or biotech manufacturing environment. Work setup: based in Raritan, NJ, with flexibility for occasional off-hours support.