Jobs · Quality Assurance · California

Quality Control Analyst II

Genentech · South San Francisco, CA · 2 wk ago
Quality AssuranceFull-time

About the role

A healthier future drives us to innovate, continuously advance science, and ensure everyone has access to the healthcare they need. In Pharma Technical Development, you will collaborate and develop creative technical solutions to efficiently transform scientific ideas into products that reliably deliver our biologics pipeline to patients.

As a Lab Analyst on our Global Analytical Development and Quality Control team, you will contribute through innovation, teamwork, and continuous improvement in a dynamic environment.

Responsibilities

  • Perform a broad variety of basic and moderately complex physico-chemical tests for biologics and other pharmaceutical compounds according to GMP.
  • Maintain accountability for deliverables affecting department goals and maintain a state of inspection readiness.
  • Identify discrepancies and support the resolution of technical problems to assist the department in meeting corporate objectives.
  • Schedule and execute routine and semi-routine assignments while supporting general lab maintenance operations.
  • Ensure the integration of environmental health, safety, and security into business processes; report any safety and environmental incidents within your functional area.
  • Adhere to cGMP policies and procedures, ensuring accurate documentation of activities and transactions in applicable systems.
  • Coordinate with customers to support operational activities and actively participate in group and project teamwork.

Requirements

  • Bachelor’s degree, preferably in a scientific discipline, or an Associate’s degree with 5 years of related experience in a lab environment.
  • Clear and effective communication, both verbally and in writing.
  • Sound judgment, reasoning, and problem-solving capabilities.
  • Attention to detail with strong organization and prioritization skills.
  • Accountability and ability to work effectively as part of a collaborative team.

Preferred Qualifications

  • Previous GMP experience in a biopharmaceutics environment.
  • QC / cGMP experience working in a lab environment in an industry or academic setting.

Relocation benefits are not available for this posting.

Pay

The expected salary range for this position based on the primary location of South San Francisco, CA is $78,500 – $145,900 USD annually. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

Benefits

This position qualifies for the benefits detailed at the provided link.

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