R&D Quality & Compliance Specialist – Hybrid (NJ)

Kenvue Inc.; Summit (NJ); Hybrid; USD 82,000 - 116,000; Full time

Benefits offered by this job

Competitive benefits package

Paid holidays and vacation

Volunteer time off

Learning & development opportunities

Kenvuer Impact Networks

Job summary

Kenvue Inc. is seeking a Specialist, R&D Quality & Compliance in Summit, NJ with a hybrid work setup. You will administer integrated quality systems to ensure R&D activities meet cGMP standards and company procedures, including documentation reviews and audits.

Responsibilities include inspection readiness, cross-functional collaboration on GMP documentation, training, and quality metrics reporting across NA sites. A strong emphasis on regulatory guidance and process improvements is required.

Qualifications

• Bachelor's degree or equivalent experience in a relevant field.
• 2–4 years in pharmaceutical, cosmetics, consumer products, or FDA-regulated environment.
• Proven ability to work effectively in a team-based environment.
• Strong organizational and communication skills; ability to handle multiple priorities.
• Proficiency with Word, Excel, PowerPoint.

Responsibilities

• Review and approve GMP documentation and batch records.
• Conduct quality inspections of supplies for R&D studies.
• Serve as Quality representative on R&D project teams.
• Provide GMP regulatory guidance and training.
• Maintain GMP documentation, storage and archival processes.
• Support GMP/Q&C procedure development and process improvements.
• Perform internal assessments and support inspection readiness.
• Collect and report NA R&D Quality metrics monthly and semiannually.
• Coordinate documentation for pre-audit requests and audit readiness.

Skills

Teamwork

Organizational skills

Communication

Multi-tasking

MS Office

Education

Bachelor's degree or equivalent experience

Tools

Microsoft Office Suite

Job description

Kenvue Inc. is seeking a Specialist, R&D Quality & Compliance in Summit, NJ with a hybrid work setup. You will administer integrated quality systems to ensure R&D activities meet cGMP standards and company procedures, including documentation reviews and audits.

Responsibilities include inspection readiness, cross-functional collaboration on GMP documentation, training, and quality metrics reporting across NA sites. A strong emphasis on regulatory guidance and process improvements is required.