Quality Control Specialist

LonzaPortsmouth, NH
Onsite

About The Position

At Lonza, a leading contract development and manufacturing organization (CDMO), our people are our greatest strength. As a global leader in life sciences, we work together to develop innovative solutions that help improve lives around the world. Through collaboration, expertise, and a commitment to quality, our teams play a critical role in bringing life-changing therapies to patients. As a QC Specialist, you will play a key role in supporting Quality Control activities within a cGMP-regulated environment. You will perform laboratory testing on in-process materials, raw materials, environmental monitoring samples, stability studies, and finished products while analyzing data and supporting investigations. This hands-on role requires strong technical skills, attention to detail, and the ability to work effectively in a fast-paced manufacturing environment. You will also contribute to continuous improvement initiatives, support quality systems, and help ensure products meet regulatory and quality requirements.

Requirements

  • Minimum of 3+ years of experience in a GMP, pharmaceutical, biotechnology, environmental, microbiology, or quality control laboratory environment
  • Experience performing laboratory testing and working with analytical or microbiological methods
  • Strong ability to analyze data, recognize trends, and investigate potential issues
  • Knowledge of cGMP regulations, data integrity principles, and documentation practices
  • Strong communication, collaboration, and problem-solving skills

Nice To Haves

  • Associate's or Bachelor's degree in a life science or related field
  • Experience using laboratory systems such as LIMS, TrackWise, DMS, or similar electronic systems

Responsibilities

  • Perform quality control testing to support manufacturing, stability programs, environmental monitoring, and product release activities
  • Execute laboratory assays and analytical techniques in accordance with approved procedures and cGMP requirements
  • Analyze and interpret data, ensuring accurate and timely reporting of results
  • Troubleshoot laboratory equipment, test methods, and system-related issues
  • Support investigations, deviations, CAPAs, and other quality system activities
  • Utilize laboratory systems such as LIMS, TrackWise, DMS, or similar electronic quality systems
  • Support training, mentoring, and knowledge sharing across the laboratory while contributing to continuous improvement initiatives

Benefits

  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Compensation programs that recognize high performance
  • Medical, dental, and vision insurance
  • Opportunities to grow and develop your career
  • A collaborative and team-focused laboratory environment
  • The opportunity to contribute to life-changing therapies
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