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Lonza

Global life sciences contract manufacturer

Biotechnologist 1

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timePortsmouth, NH, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or equivalent experience is required.
  • Confirmed working experience in manufacturing is required; experience in a current good manufacturing practice (cGMP) setting or as a BioPharma Associate Level I is preferred.
  • Demonstrated logical decision-making abilities and critical-thinking skills are required.
  • Strong written and verbal communication skills are required.
  • Flexibility to adapt to changing business priorities is required.
  • Associates must actively seek and implement feedback to improve performance.

Responsibilities

  • Operate and maintain equipment, supervise production processes, and report production in written and electronic formats.
  • Follow good manufacturing practices (GMPs) and good documentation practices (GDPs), troubleshoot issues, and review documentation to ensure compliance.
  • Perform suite-specific production activities and laboratory tasks, including bioreactor inoculation and chromatography column operation, and apply the scientific theories behind these processes.
  • Train other associates on assigned tasks and related theories as needed.
  • Attend shift exchanges and meetings, send and receive emails, and engage in projects.
  • Complete technical writing, including documenting deviations and completing document change forms.
  • Attain and maintain qualification for assigned tasks and adhere to an individual training plan.
  • Transfer raw materials and chemicals into, out of, and across production areas.
  • Perform other duties as assigned.

Desired Qualifications

  • An Associate or Bachelor's degree in a scientific field is preferred.
  • Experience in a cGMP setting or as a BioPharma Associate Level I is preferred.

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

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