Hybrid R&D Quality & Compliance Specialist

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

Benefits offered by this job

Competitive Benefits Package

Holidays and vacation

Volunteer Time & More

Learning & Development

Kenvuer Impact Networks

Job summary

Kenvue is hiring a Specialist, R&D Quality & Compliance in Summit, New Jersey. Hybrid work location with a focus on administering integrated quality systems to ensure R&D functions meet cGMP and company procedures.

Responsibilities include documentation review, audits, study releases support, and regulatory guidance, with QA representation on project teams and ongoing training for personnel in Quality processes.

Qualifications

• Bachelor's degree or equivalent experience required.
• 2–4 years in pharmaceutical, cosmetics, consumer products, or FDA-regulated environment.
• Ability to work effectively in a team-based environment and manage multiple priorities.
• Strong communication, interpersonal and facilitation skills.

Responsibilities

• Review and approve GMP documentation and batch records for R&D studies.
• Conduct quality inspections of supplies used in R&D studies.
• Serve as Quality representative on R&D project teams and provide GMP regulatory guidance.
• Maintain GMP documentation, storage and archival processes and support audits.

Skills

Team-based environment

Organizational skills

Communication skills

MS Office proficiency

Education

Bachelor's degree in a relevant field

Tools

Microsoft Office (Word, Excel, PowerPoint)

Job description

Kenvue is hiring a Specialist, R&D Quality & Compliance in Summit, New Jersey. Hybrid work location with a focus on administering integrated quality systems to ensure R&D functions meet cGMP and company procedures.

Responsibilities include documentation review, audits, study releases support, and regulatory guidance, with QA representation on project teams and ongoing training for personnel in Quality processes.