Global Laboratory Quality & Data Systems Specialist

Outlier; Quilmes; On-site; ARS 92,241,000 - 138,361,000; Full time

Job summary

IQVIA Laboratories in Buenos Aires, Argentina is seeking an Operational Quality Specialist to support global laboratory quality systems, oversee assay QC processes and proficiency testing, and coordinate across labs, data management, and vendors.

You will review acceptance criteria, manage the scientific database, monitor inventory of reagents/controls, and deliver trainings while collaborating with assay development and management teams to ensure quality and operational excellence.

Qualifications

• Bachelor's Degree in medical technology or equivalent required.
• 3 years experience in a research laboratory/clinical laboratory environment required.
• Knowledge of laboratory equipment, clinical laboratory assays, quality control, and validation procedures.
• Advanced Excel spreadsheet skills.
• Other Equivalent combination of education, training, and experience may be accepted in lieu of degree.

Responsibilities

• Establish, review, and update global acceptance criteria for harmonized assay quality control materials.
• Monitor and review regional laboratory investigations related to proficiency testing failures.
• Maintain and update the Scientific Database, including test code system administration.
• Monitor global inventory levels of harmonized reagents, calibrators, and quality control materials.
• Deliver training to Global Harmonization and regional laboratory teams as needed.
• Facilitate and document global technical meetings.
• Collaborate with assay development, scientific review, data management, vendor, and laboratory management teams.

Skills

Advanced Excel

Laboratory experience

Education

Bachelor's Degree in medical technology

Job description

IQVIA Laboratories in Buenos Aires, Argentina is seeking an Operational Quality Specialist to support global laboratory quality systems, oversee assay QC processes and proficiency testing, and coordinate across labs, data management, and vendors.

You will review acceptance criteria, manage the scientific database, monitor inventory of reagents/controls, and deliver trainings while collaborating with assay development and management teams to ensure quality and operational excellence.