7 Quality Assurance And Engineering jobs in Buenos Aires.

Hiring now: Sr Regulatory Affairs Ass @ Parexel, Regulatory Reporting Spec @ Iqvia, Sr Quality Auditor @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (3) Project Management (2) Quality Management (2) compliance (2) Health Care (2) Site Activation (2) Regulatory Affairs (1) Consulting (1) Biologics (1) Publishing (1)

đź“Ť Locations

Buenos Aires (7)
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Parexel

Senior Regulatory Affairs Associate, Labelling Buenos Aires
Skills & Focus: Regulatory Affairs, Consulting, Clinical Trials, Biologics, Project Management, Publishing, Submissions, Labeling, CMC, Quality Management
About the Company: Parexel is a global biopharmaceutical services provider with a comprehensive portfolio of solutions to help clients navigate the clinical development process.
Type: Remote

Iqvia

Regulatory Reporting Specialist Buenos Aires
Skills & Focus: pharmacovigilance, regulatory reporting, safety data, compliance, quality, team, medical terminology, project requirements, organizational skills, attention to detail
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Up to 3 years of experience in pharmacovigilance activities
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Syneos Health

Senior Quality Auditor Buenos Aires
Skills & Focus: Quality Auditor, Clinical Trials, GCP Audits, Vendor Audits, Audit Reports, Documentation, Health Care, Clinical Quality Assurance, Communication Skills, Regulatory Violations
About the Company: Syneos Health is a fully integrated biopharmaceutical solutions organization, designed to address new market realities, where clinical and commercial expertise…
Experience: Extensive experience in clinical quality assurance auditing and conduct of vendor audits.
Benefits: Competitive compensation package, Health benefits including Medical, Dental and Vision, flexible paid time off (PTO).
Associate Director, Engineering Buenos Aires
Skills & Focus: line management, technical expertise, SDLC, data management, project management, leadership, biopharmaceutical, compliance, cloud, team development
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: significant information systems/technology experience in a data intensive operational and compliance environment

Iqvia

FSP - Sr. Regulatory & Start Up Specialist Buenos Aires
Skills & Focus: Regulatory, Site Activation, Clinical Research, SOPs, Quality Control, Document Management, Compliance, Project Management, International Regulations, Health Care
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: +3 years of clinical research experience within regulatory area in Argentina
Type: Full time
FSP Regulatory and Start Up Specialist Buenos Aires
Skills & Focus: Site Activation, regulations, standard operating procedures, feasibility, site ID, start up, site activation activities, quality control, project planning, Informed Consent Form
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: +1 years’ of relevant experience working in the regulatory department in Argentina
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Quality Manager, cFSP Buenos Aires
Skills & Focus: Quality Management, Clinical Trials, Inspection Readiness, Risk Management, Regulatory Compliance, GCP, Process Improvement, Stakeholder Engagement, Continuous Improvement, Cross-functional Collaboration
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Minimum of 5 years’ experience in a pharmaceutical, bio-pharmaceutical, or Contract Research Organization company, or equivalent. Minimum of 3 years’ experience in quality role.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.