Quality Systems Analyst: Drive Compliance & Process

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

Job summary

Johnson & Johnson is seeking an Analyst, Quality Systems to join our quality organization in Raritan, NJ. The role will support quality system execution, document lifecycle, and site-wide compliance within a fast-paced manufacturing environment.

The ideal candidate will have at least 2 years of QA/Quality Systems experience, knowledge of cGMP regulations, and excellent written and verbal communication skills to collaborate across functions and sites.

Qualifications

• Bachelor's degree in engineering, science or equivalent.
• Minimum 2 years of work experience in Quality Assurance/Quality Systems/Quality Control/Quality related activities.
• Knowledge of cGMP regulations.
• Experience in a highly paced manufacturing environment (preferred).

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 safety policies, quality systems and cGxP requirements.

Skills

Strong written & verbal English

Collaboration & time management

Education

Bachelor's degree in engineering, science or equivalent

Job description

Johnson & Johnson is seeking an Analyst, Quality Systems to join our quality organization in Raritan, NJ. The role will support quality system execution, document lifecycle, and site-wide compliance within a fast-paced manufacturing environment.

The ideal candidate will have at least 2 years of QA/Quality Systems experience, knowledge of cGMP regulations, and excellent written and verbal communication skills to collaborate across functions and sites.