Night-Shift QC Analyst II – Analytical

Lonza; Portsmouth (NH); On-site; Confidential; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Professional growth opportunities

Collaborative cross-team environment

Job summary

Lonza in Portsmouth, NH is seeking a QC Analyst II for the night shift to support testing of materials, in-process samples, and finished products. You will deliver timely results to enable product release and maintain quality records in a regulated lab.

Applicants should have an associate degree in Life Sciences and experience in a cGMP setting, with strong data analysis, communication, and collaboration skills. This role emphasizes teamwork and continuous improvement.

Qualifications

• Experience in a regulated laboratory or cGMP environment.
• Ability to analyze data and identify trends or issues.
• Strong organizational and multi-tasking abilities.
• Effective written and verbal communication in a team setting.

Responsibilities

• Perform testing of raw materials, in-process samples, finished products, and stability samples to support product quality.
• Deliver accurate and timely laboratory results to support manufacturing operations and product release.
• Review analytical data and documentation to ensure compliance with quality standards.
• Document laboratory activities, investigations, and quality records in accordance with established procedures.
• Maintain laboratory materials, supplies, and organization to support efficient operations.
• Develop knowledge in environmental monitoring, biochemistry, and microbiology testing methods.
• Collaborate with Quality, Manufacturing, and technical teams to support continuous improvement and operational excellence.

Skills

Data analysis

Organizational skills

Communication

Collaboration

Quality mindset

Education

Associate's degree in Life Sciences

Job description

Lonza in Portsmouth, NH is seeking a QC Analyst II for the night shift to support testing of materials, in-process samples, and finished products. You will deliver timely results to enable product release and maintain quality records in a regulated lab.

Applicants should have an associate degree in Life Sciences and experience in a cGMP setting, with strong data analysis, communication, and collaboration skills. This role emphasizes teamwork and continuous improvement.