Quality Control Specialist I – NGS & GMP (Contract)

Freenome; California; Híbrido; USD 48 000 - 83 000; Tempo integral

Resumo da oferta

Freenome in Brisbane, California is seeking a Quality Control Specialist I (Contractor) to perform reagent QC testing per SOPs, author and maintain regulatory documentation, and support method transfer and QC data trending in a CLIA-regulated lab. This onsite role reports to the Quality Control Supervisor.

Candidates should have a Bachelors degree in a life science, strong attention to detail, excellent documentation skills, and the ability to work in a cross-functional, regulated environment.

Qualificações

• Bachelors degree in a life sciences field.
• Ability to follow written procedures in regulated environments.
• Accurate and timely documentation for regulatory compliance.
• Strong attention to detail and time management.
• Excellent interpersonal and communication skills in cross-functional settings.

Responsabilidades

• Perform reagent quality control testing per Standard Operating Procedures.
• Author, review, and maintain documentation such as SOPs, Work Instructions, QC Records and Forms for regulatory compliance.
• Initiate non-conformances for any process deviations or QC failures.
• Participate in investigations of reagent and consumable quality issues.
• Record, analyze, and trend QC data using good documentation practices.
• Support tech transfer and validation of QC test methods to GMP standards.
• Build and maintain knowledge of regulatory requirements for lab operations and QC.

Conhecimentos

Attention to detail

Regulated environment

Documentation

Cross-functional collaboration

Time management

Formação académica

Bachelors degree in Chemistry, Biochemistry, Biology, Bioengineering or similar

Ferramentas

Excel

Word

PowerPoint

Hamilton

Bravo

Descrição da oferta de emprego

Freenome in Brisbane, California is seeking a Quality Control Specialist I (Contractor) to perform reagent QC testing per SOPs, author and maintain regulatory documentation, and support method transfer and QC data trending in a CLIA-regulated lab. This onsite role reports to the Quality Control Supervisor.

Candidates should have a Bachelors degree in a life science, strong attention to detail, excellent documentation skills, and the ability to work in a cross-functional, regulated environment.