5 Quality Engineering jobs in Québec.

Hiring now: Regulatory Affairs Consul @ Parexel, Sr Auditor Qa Temporary @ Syneos Hea, Gestionnaire Système Qual @ Bd.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Affairs (3) Medical Device (3) Consulting (2) Labeling Operations (2) Drug & Device (2) Long term temp (2) Audits (2) Biologics (2) Remote (2) Clinical (1)

📍 Locations

Québec (5)
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Parexel

Regulatory Affairs Consultant Québec
Skills & Focus: Regulatory Affairs, Consulting, Medical Device, Clinical, Labeling Operations, Home Based, East Coast, Drug & Device, Long term temp, Functional Service Provider

Syneos Health

Sr. Auditor QA (Temporary) Québec
Skills & Focus: Quality Assurance, Audits, Regulatory Authority Inspections, GxP, Audit Reports, Training, Vendor Audits, Communication, Problem Solving, Documentation
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Requires a Bachelor’s degree in the science/health care field or equivalent with extensive experience in GxP quality assurance auditing.
Type: Temporary
Benefits: Career development and progression; supportive management; training; peer recognition; total rewards program.

Parexel

Regulatory Affairs Consultant, Biologics Québec
Skills & Focus: Regulatory Affairs, Biologics, Consulting, Clinical Trials, Remote, Medical Device, Publishing, Senior Associate, Technical, Drug & Device
About the Company: Parexel is a global clinical research organization that provides expertise in regulatory affairs, medical writing, and clinical trials management.
Type: Remote
Various Regulatory Operations Positions Québec
Skills & Focus: Regulatory Affairs, Consultant, Project Management, Submissions, CMC, Medical Device, Long term temp, Labeling Operations, Biologics, Remote
About the Company: Parexel is a global biopharmaceutical services organization that helps companies bring new therapies to market while optimizing the development process.
Type: Full-time

Bd

Gestionnaire Système Qualité Québec
Skills & Focus: Quality Management, Regulatory Compliance, Quality Systems, Non-conformities, Audits, Document Control, Corrective Actions, Training Management, Biotechnology, Medical Devices
About the Company: BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and…
Experience: 5-7 years in the medical devices industry or related biotechnology fields
Salary: Competitive
Type: Full-Time
Benefits: Healthcare, 401(k)/ Retirement Plans, Professional Development, Paid Time Off, Awards & Recognition