QA Specialist II - 2nd Shift: Quality & Compliance

Kenvue; Lititz (Lancaster County); On-site; USD 73,000 - 103,000; Full time

Benefits offered by this job

Competitive Benefit Package

Paid Company Holidays

Paid Vacation

Volunteer Time & More!

Learning & Development Opportunities

Job summary

Kenvue in Lititz, PA is seeking a QA Specialist II (2nd Shift) to perform product releases and ensure compliance with GMP, GLP and local regulations. You will review records, investigate non-conformances, and provide QA support to manufacturing and packaging operations.

This onsite role requires a Bachelor’s degree and GMP experience; strong communication, analytical skills, and the ability to influence cross‑functional teams.

Qualifications

• Ability to communicate thoughts and ideas effectively—verbal and written.
• Strong analytical skills to develop quality strategies and ensure regulatory compliance.
• Demonstrated ability to accomplish work goals.

Responsibilities

• Review production records for manufacturing, packaging, and lab documents.
• Release finished products based on conformance to established standards.
• Apply QA processes, procedures, and activities.
• Conduct GMP area walkthroughs and assessments.
• Collaborate with Operations to address quality issues and improvements.
• Review batch records for investigations and non-conformances.
• Generate certificates of compliance for foreign affiliates.
• Lead process improvement teams as appropriate.
• Maintain ownership of SOPs and assist in updates.
• Support regulatory audits and agency visits.

Skills

Communication skills

Analytical skills

Goal‑oriented

Problem solving

Education

Bachelor's Degree

Tools

Word

Excel

Job description

Kenvue in Lititz, PA is seeking a QA Specialist II (2nd Shift) to perform product releases and ensure compliance with GMP, GLP and local regulations. You will review records, investigate non-conformances, and provide QA support to manufacturing and packaging operations.

This onsite role requires a Bachelor’s degree and GMP experience; strong communication, analytical skills, and the ability to influence cross‑functional teams.