Quality Systems Analyst 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:
Site liaising.
Document lifecycle management.
SOP updates.
Project leadership.
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.
Risk identification in a regulated pharmaceutical or biotech manufacturing environment.
Work setup Based in Raritan, NJ, with flexibility for occasional off-hours support.
