QC Analyst Trainee - Biologics & GMP Testing

WuXi Biologics

Cranbury Township (NJ)

On-site

USD 28,000 - 39,000

Full time

26 hours ago
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Job summary

WuXi Biologics invites applications for its QC Analyst Training Program in Cranbury, NJ. The program develops early-career scientists into QC analysts, spanning physicochemical testing, bioassay and impurity analysis for biologics.

Trainees complete theory and supervised lab practice, qualification, and lifecycle activities under cGMP and ALCOA+ data integrity principles. Participants advance through structured modules, including GMP compliance, documentation practices, and method transfer, with

Qualifications

  • Hands-on laboratory experience through coursework, internships, or work in biotech/pharma.
  • Understanding of GMP, data integrity, and Good Documentation Practices.
  • Ability to follow controlled procedures and organize scientific data.
  • Effective written and verbal communication and ability to work independently in a fast-paced lab environment.

Responsibilities

  • Complete training curriculum, laboratory rotations, and method qualifications.
  • Perform physicochemical, biochemical, bioassay, and residual-impurity testing per approved methods and cGMPs.
  • Support in-process, release, stability, characterization, and comparability testing; organize and trend results for assigned procedures.
  • Review test records, calculations, chromatograms, and supporting documentation for accuracy and data integrity.

Skills

Laboratory skills
Data integrity
Documentation
Communication

Education

Associate or bachelor’s degree in Chemistry/Biochemistry/Biology/Biotech/Pharma/Engineering

Tools

Empower
SoftMax
LIMS

Job description

WuXi Biologics invites applications for its QC Analyst Training Program in Cranbury, NJ. The program develops early-career scientists into QC analysts, spanning physicochemical testing, bioassay and impurity analysis for biologics.

Trainees complete theory and supervised lab practice, qualification, and lifecycle activities under cGMP and ALCOA+ data integrity principles. Participants advance through structured modules, including GMP compliance, documentation practices, and method transfer, with

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