Quality Control Specialist — On-Site Lab Innovator

Lonza Group Ltd.; Portsmouth (NH); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Insurance

Career development

Team environment

Impactful therapies

Job summary

Lonza Group Ltd. is seeking a Quality Control Specialist to join our on-site laboratory in Portsmouth, NH. You will perform QC testing on in-process materials, raw materials, environmental monitoring samples, stability studies, and finished products in a fast-paced, cGMP setting.

The role requires strong technical skills, attention to detail, and collaboration with a cross-disciplinary team. You will contribute to investigations, data analysis, and continuous improvement initiatives while

Qualifications

• Associate's or Bachelor's degree in life science or related field preferred.
• Minimum 3+ years in GMP/pharma/biotech QA or QC lab.
• Experience with laboratory testing and analytical methods.
• Experience with LIMS/TrackWise/DMS or similar systems preferred.
• Strong data analysis and trend investigation skills.
• Knowledge of cGMP regulations and documentation practices.

Responsibilities

• Perform QC testing to support manufacturing, stability programs, environmental monitoring, and product release activities.
• Execute laboratory assays and analytical techniques per approved SOPs in a cGMP environment.
• Analyze data and report results accurately and timely.
• Troubleshoot laboratory equipment, methods, and system-related issues.
• Support investigations, deviations, CAPAs, and other quality system activities.
• Utilize laboratory information systems (LIMS, TrackWise, DMS) and contribute to continuous improvement.

Skills

Quality control

GMP experience

Data analysis

Troubleshooting

Communication

Education

Associate/Bachelor in life science

Tools

LIMS

TrackWise

DMS

Job description

Lonza Group Ltd. is seeking a Quality Control Specialist to join our on-site laboratory in Portsmouth, NH. You will perform QC testing on in-process materials, raw materials, environmental monitoring samples, stability studies, and finished products in a fast-paced, cGMP setting.

The role requires strong technical skills, attention to detail, and collaboration with a cross-disciplinary team. You will contribute to investigations, data analysis, and continuous improvement initiatives while