Quality Systems Analyst: Elevate Data Integrity & Compliance

Regulatory Jobs; Raritan (NJ); On-site; USD 65,000 - 105,000; Full time

Job summary

Johnson & Johnson in Raritan, New Jersey, is seeking two Analyst Quality Systems to strengthen our quality governance across site activities. You will execute quality system processes, manage documents, and support data integrity within cGMP frameworks.

Join a fast-paced manufacturing environment where you collaborate across functions, drive improvements, and lead selected projects through to closure while maintaining compliance and quality standards.

Qualifications

• Minimum 2 years in Quality Assurance/Quality Systems/Quality Control or related activities.
• Knowledge of cGMP regulations.
• Degree in engineering, science or a related technical field.

Responsibilities

• Complete quality system execution activities, including document/records management and data integrity.
• Act as a liaison between site and above-site activities.
• Support document lifecycle and perform site superuser activities.
• Identify improvement opportunities and elevate potential risks to management.
• Actively assist in Audit, Investigation and Change Control related activities.
• Participate in department optimization efforts.
• Take the lead on selected projects assignments following them through closure.
• Update Standard Operating Procedures and related documents.
• Drive alignment and efficiencies between local and global processes.
• Perform tasks in a manner consistent with the safety policies, quality systems and cGxP requirements.
• Provide occasional support at off-shift hours with little or no prior notice.
• Other duties can be assigned to support business continuity.

Skills

English skills

Collaboration

Time management

Education

Bachelor's degree in engineering, science, or equivalent

Job description

Johnson & Johnson in Raritan, New Jersey, is seeking two Analyst Quality Systems to strengthen our quality governance across site activities. You will execute quality system processes, manage documents, and support data integrity within cGMP frameworks.

Join a fast-paced manufacturing environment where you collaborate across functions, drive improvements, and lead selected projects through to closure while maintaining compliance and quality standards.