QA Analyst - Torrance CA

$52,000 - $60,320/Yr

Kelly Services - Torrance, CA

posted 3 months ago

Full-time - Entry Level
Torrance, CA
Administrative and Support Services

About the position

The Quality Assurance Analyst position in Torrance, CA, is a critical role within the laboratory environment, focusing on ensuring the highest standards of quality assurance and quality control. This position is temp to hire, offering a competitive hourly wage of $25-29. The QA Analyst will work closely with the QA Director to implement and maintain quality programs that comply with corporate standards and laboratory accreditation requirements. The role requires a proactive approach to quality management, ensuring that all laboratory processes meet regulatory and internal standards. In this position, the QA Analyst will be responsible for reviewing raw data and analytical reports to ensure accuracy and compliance with established protocols. Daily verification of Chemistry and Microbiology balances is a key responsibility, as is overseeing the receipt of DEA samples from clients and managing the Controlled Substance program. The QA Analyst will also coordinate the disposal process for controlled substances, ensuring that all actions are compliant with regulatory requirements. The role involves reviewing and approving deviations, Out of Specification (OOS) investigations, and proposals for Corrective and Preventive Actions (CAPA). The QA Analyst will be expected to revise procedures relevant to their expertise and participate in training sessions for quality, laboratory, and administrative staff as needed. Adherence to current Standard Operating Procedures (SOPs) and practicing proper current Good Documentation Practices (cGDP) are essential components of this role. The QA Analyst will also be expected to perform other duties as required, contributing to the overall success of the laboratory's quality assurance efforts.

Responsibilities

  • Review raw data and associated analytical reports for accuracy and compliance.
  • Perform daily verification of Chemistry and Microbiology balances.
  • Oversight of DEA sample receipt from Clients, Controlled Substance program management, and coordination of disposal process.
  • Perform review/approval of Deviations, OOS Investigations, Corrective/Preventive Action (CAPA) proposals, and other requests as assigned.
  • Revise procedures relevant to job description and expertise.
  • Participate in training of quality, laboratory, and administrative staff as needed.
  • Perform all duties following current SOPs.
  • Practice proper cGDP.
  • Other duties as required.

Requirements

  • Bachelor's degree in life sciences with 0-2 years of relevant laboratory/pharmaceutical industry experience.
  • Familiarity with electronic Document Control system (e.g., CompliantPro) preferred.
  • Knowledge of documentation functions within a cGMP or ISO regulated environment.
  • Good communication and organizational skills.
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