Manufacturing Quality & Sensory Lead

Ecolab; Quilmes; On-site; ARS 900,000 - 1,300,000; Full time

Job summary

IQVIA Laboratories in Buenos Aires, Argentina is seeking an Operational Quality Specialist to join our team. You will establish, review, and update global acceptance criteria for harmonized assay quality control materials and collaborate across regional labs.

The role requires a Bachelor's in medical technology, 3 years in a research or clinical lab, and advanced Excel skills. You will monitor investigations, manage the scientific database, inventory levels, and deliver training while supporting

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.

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

Laboratory knowledge

Quality control procedures

Safety procedures

Education

Bachelor's Degree in Medical Technology

Tools

Excel

Job description

Buenos Aires, Argentina
Full time
R

Job Summary

We are seeking Operational Quality Specialist to join IQVIA Laboratories at Buenos Aires, Argentina.

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

What You'll Be Doing

• 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

What We Are Looking For

• 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

The Knowledge, Skills and Abilities Needed for This Role

• Knowledge of clinical and/or research laboratory environments, including safety and infection control procedures
• Ability to balance multiple priorities while maintaining quality and accuracy
• Ability to establish and maintain effective working relationships with coworkers, managers, clients, and cross-functional stakeholders

What We Offer You

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

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