9 publicaciones de empleo destacadas de people program specialist en buenos aires, b (¡Están contratando!)

Lab Technical Specialist
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
13h
Safety Specialist I - Mexico and Argentina - Hybrid
サイネオス・ヘルス —Buenos Aires, Buenos Aires
6d
Senior Quant Developer
SimCorp A/S —Buenos Aires, Buenos Aires
- Tiempo completo
Técnico de Ascensores
Otis —Capital Federal, Buenos Aires
- Tiempo completo
Tax Advisory Specialist
ExxonMobil —Capital Federal, Buenos Aires
Senior Business Analyst
EY —Capital Federal, Buenos Aires
Sr. Safety Specialist
サイネオス・ヘルス —Buenos Aires, Buenos Aires
7d
Field Specialist - Mechanical Gas / Steam Turbine / Compressors
Baker Hughes —Buenos Aires, Buenos Aires
Associate Study Start Up Manager
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
7h

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Lab Technical Specialist

IQVIA -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo
Hace 13 horas

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Hybrid | R1563354

We are seeking Lab Technical 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.

Job Summary:

The Lab Technical Specialist monitors the performance and reporting of laboratory assays by supporting quality control, validation, proficiency testing, regulatory schedules and technical documentation. This role provides technical expertise to strengthen laboratory quality, operational efficiency and compliance with applicable standards.

What You'll Be Doing:

Develop and maintain the local laboratory Quality Control Program and database, including statistical analysis and quality control performance data reviews in accordance with policy and regulatory guidelines
Validate assays through statistical analysis of local laboratory data, troubleshooting analytical methods and providing technical information to relevant parties
Manage proficiency testing and accreditation program activities, including enrollment, submission, review and investigations
Develop yearly schedules for regulatory functions and perform data analysis for linearity, comparison or other required studies
Act as a technical subject matter expert and liaise with IT and systems teams to support appropriate functionality
Draft new standard operating procedures and maintain existing SOPs related to departmental activities on a regional or global basis
Support audits, inspections, process improvements, troubleshooting, safety requirements and 6S initiatives

What We Are Looking For:

Bachelor’s Degree in life sciences or another relevant field is required
1 year of experience in a clinical, research, academic or commercial/production laboratory environment
Knowledge of relevant regulatory agency standards
Knowledge of laboratory equipment, clinical laboratory assays, quality control and validation procedures
Strong technical knowledge of complex testing procedures and the science supporting the analysis
Proficiency with complex laboratory calculations, including averages, means, standard deviations and various quality control metrics
Other Equivalent combination of education, training, and experience may be accepted in lieu of degree

The Knowledge, Skills and Abilities Needed for This Role:

Good computer skills, including proficiency with Microsoft Excel, PowerPoint and Word
Effective organizational, interpersonal, communication and presentation skills
Strong attention to detail and accuracy
Ability to work independently as well as in a team environment
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Applicable certifications and licenses as required by local regulations

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.

To learn more about our benefits, visit IQVIA benefits.

If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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