Quality Control Jobs at Lonza, US
Lonza is hiring a QC Analyst Level 1 – Environmental Monitoring to support high-quality pharmaceutical manufacturing at its Portsmouth, New Hampshire facility. The Quality Control Jobs at Lonza are ideal for entry-level to early-career quality control professionals looking to build hands-on experience in GMP testing, environmental monitoring, and quality systems within a global life sciences organization. The candidate getting selected for the QC Analyst job will play a critical role in ensuring safe, compliant, and timely production of drug products.
Job Details:
- Job Title: QC Analyst Level 1 – Environmental Monitoring
- Reference ID: R70850
- Location: Portsmouth, New Hampshire, United States
- Job Type: Full-Time
- Work Schedule: 10-hour Day Shifts
- Department: Quality Control
- Industry: Life Sciences / Pharmaceutical Manufacturing
About the Company:
Lonza is a global leader in life sciences, operating across three continents and serving customers worldwide. The company enables pharmaceutical, biotech, and specialty ingredient industries to bring innovative products to market. At Lonza, employees are empowered to own their careers while contributing to work that improves lives globally. Ethical practices, environmental responsibility, and people-focused values are at the core of Lonza’s success.
Educational Requirements for the QC Analyst Role:
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Bachelor’s or Associate’s degree (preferred) in:
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Microbiology
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Biochemistry
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Life Sciences or a related scientific discipline
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Key Responsibilities of the QC Analyst:
- Perform environmental monitoring and quality control testing for in-process, lot release, and stability studies
- Run and review test samples in accordance with approved GMP procedures
- Review assays and analytical test results for accuracy and compliance
- Prepare and maintain quality documentation including Deviations, CAPA, Change Controls, and test methods
- Support QC activities to meet manufacturing and customer timelines
- Use laboratory computer systems and GMP quality platforms for data recording
- Perform additional quality-related duties as assigned
Skills Required for the QC Analyst Role:
- Working knowledge of GMP laboratory operations
- Familiarity with environmental monitoring and microbiological testing
- Experience with LIMS, TrackWise, or similar quality systems (preferred)
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong attention to detail and ability to recognize deviations
- Analytical thinking and problem-solving skills
- Ability to work independently on semi-routine laboratory tasks
Benefits of the Quality Control Jobs:
- Opportunity to work with a global life sciences leader
- Hands-on experience in GMP Quality Control and Environmental Monitoring
- Career growth and development in pharmaceutical manufacturing
- Inclusive and ethical workplace culture
- Meaningful work contributing to products that impact millions of lives
- Equal opportunity employer with a strong commitment to diversity and safety
