L

Lonza

Global life sciences contract manufacturer

QC Analyst 2 - Cell Therapy

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timePortsmouth, NH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in biology, microbiology, biochemistry, or another relevant scientific discipline, or a comparable combination of an associate degree and experience.
  • Two or more years of relevant laboratory or Quality Control experience.
  • Experience working in a regulated laboratory or cGMP environment.
  • Experience with biological materials, cell-based assays, or related analytical testing.
  • Ability to interpret laboratory data and recognize unexpected results.
  • Strong attention to detail, organization, and documentation skills.
  • Effective communication and collaboration skills.
  • Ability to work Sunday through Wednesday from 11:00 AM to 9:30 PM in an environment requiring appropriate gowning.

Responsibilities

  • Perform in-process and release testing on patient-specific material.
  • Conduct cell count, viability, endotoxin, and other applicable Quality Control testing.
  • Deliver accurate and timely laboratory results to support manufacturing and product release.
  • Review analytical data and identify unexpected results or issues requiring escalation.
  • Document laboratory activities and test results in accordance with cGMP requirements.
  • Support environmental monitoring activities, including plating and incubations.
  • Maintain laboratory materials, equipment, supplies, and work areas.
  • Collaborate with Quality Control, Environmental Monitoring, Cell Therapy, and Manufacturing teams.
  • Contribute to laboratory problem-solving and continuous improvement.

Desired Qualifications

  • Flow cytometry experience.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

Recently Posted Jobs

Explore more opportunities at Lonza

See more jobs