31 Quality Engineering jobs in Toronto.

Hiring now: Rd Engr I @ Boston Sci, Sr Dir Regulatory Affairs @ Novo Nordi, Quality Assurance Mgr @ Alphora, Mgr Mktg Global Infusion @ Baxter, Associate Dir Regulatory @ Astrazenec, Proj Mgr @ Eurofins C, Associate Dir Regulatory @ Alexion, Quality System Spec Clini @ Profound M, Formulation Chemist @ Eurofins A, Sr Mgr Medical Writing @ Jazz Pharm.Explore more at jobswithgpt.com.

🔥 Skills

Compliance (8) Regulatory Affairs (6) Regulatory Compliance (4) compliance (4) pharmaceutical (4) project management (4) Project Management (3) Regulatory (3) SOPs (3) risk management (3)

📍 Locations

Mississauga (22) Toronto (6) Oakville (3)

Boston Scientific

R&D Engineer I Mississauga
Skills & Focus: medical devices, design, prototyping, validation, manufacturing, regulatory approval, intellectual property, design requirements, communication skills, engineering
About the Company: At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling so…
Experience: 1-2 years
Salary: $49,700 - $98,900
Type: Contract

Novo Nordisk

Skills & Focus: Regulatory Affairs, Patient Safety, Pharmacovigilance, Health Canada, Compliance, Budgets, Team Development, Project Management, Health Authority Audits, Regulatory Compliance
About the Company: Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat serious chronic dis…
Experience: At least 5 years of experience working in Pharmacovigilance/Patient Safety, including a minimum of five years as a People Manager.

Boston Scientific

Skills & Focus: R&D, Labeling, Medical Device, Technical Leadership, Compliance, Regulatory, Cross-Functional, Sustainability, Team Leadership, Innovation
About the Company: At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling so…
Experience: 5-7 years in the medical device industry, minimum 3 years of people management and technical leadership experience
Salary: $79,700 - $158,200
Type: Hybrid
Benefits: Core and optional employee benefits including variable compensation.

Novo Nordisk

Skills & Focus: Regulatory Affairs, Patient Safety, Pharmacovigilance, Health Canada, compliance, strategic initiatives, budget management, team development, health authority audits, innovation
About the Company: Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Its purpose is to drive change to defeat serious chronic dis…
Experience: At least 5 years in Pharmacovigilance/Patient Safety, including a minimum of five years as a People Manager.

Alphora

Skills & Focus: Quality Management Systems, GMP, Batch Manufacturing, SOPs, Deviation Management, Root Cause Analysis, CAPA, Regulatory Compliance, Audit Support, Analytical Data Review
Experience: 5+ years in Quality Assurance, specifically in Biologics or Pharmaceuticals
Type: Full-time

Baxter

Skills & Focus: Marketing, Global, Infusion, Systems, Manager, Compliance, Healthcare, Innovation, Therapies, Products
About the Company: Baxter International Inc. is a global healthcare company that provides a broad portfolio of essential renal and hospital products and services.
Type: Full time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.

Boston Scientific

R&D Engineer III Mississauga
Skills & Focus: R&D, Biomedical Engineering, product life cycle, mechanical designs, risk management, ISO 13485, design control, complaint analysis, cross-functional teams, project planning
About the Company: At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling so…
Experience: 4+ years of related working experience
Salary: $66,500 - $131,800
Type: Hybrid
Benefits: Core and optional employee benefits offered, including compensation variability.

Astrazeneca

Skills & Focus: regulatory processes, compliance, drug development, collaboration, process improvement, technology, standard operating procedures, Veeva Vault, quality system, Key Performance Indicators
About the Company: A global biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines, particularly for areas such as Oncol…
Experience: At least 10 years relevant experience
Type: Full-time

Eurofins Cdmo Alphora

Project Manager Mississauga
Skills & Focus: Project Manager, pharmaceutical sector, planning, execution, project delivery, cross-functional teams, budgets, quality compliance, client communication, project evaluation

Boston Scientific

Skills & Focus: R&D Engineer, Biomedical Engineering, Electrophysiology, Design Control, ISO 13485, ISO 14971, People Management, Technical Leadership, Cross-Functional Collaboration, Project Management
About the Company: A global leader in medical science committed to advancing science for life, transforming lives through innovative medical solutions that improve patient lives.
Experience: 6+ years of relevant work experience
Salary: $79,700 - $158,200
Type: Hybrid
Benefits: Employee benefits include variable compensation, annual bonus target, and core employee benefits; see company benefits …

Astrazeneca

Skills & Focus: clinical, regulatory, writing, communications, leadership, medical, pharmaceutical, documents, strategic, quality
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: Experience in medical communications.
Type: Full-time
Benefits: AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion.

Alexion

Skills & Focus: Regulatory Affairs, Compliance, Quality System, Performance Indicator, Regulatory Processes, Collaboration, Veeva Vault, Drug Development, Standard Operating Procedures, Change Management
About the Company: AstraZeneca Rare Disease is committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible,…
Experience: At least 10 years relevant experience
Type: Full-time

Profound Medical

Skills & Focus: Quality Management System, Quality Assurance, Regulatory Compliance, Training, Document Control, Design History Files, Quality Control, Supplier Management, Internal Quality Audits, Medical Device Regulations
About the Company: A company focused on innovating medical device solutions for precision ablation of tissue, aiming to change the standard of care for conditions such as prostat…
Experience: Minimum 3 years medical device experience
Type: Full-Time

Astrazeneca

Skills & Focus: GCP, Quality Management, Clinical Research, Regulatory Compliance, Risk Assessments, Mentoring, Stakeholder Engagement, Continuous Improvement, GxP Inspections, Team Leadership
About the Company: AstraZeneca is one of the world's most forward-thinking and connected BioPharmaceutical companies, focused on delivering life-changing medicines.
Experience: 15+ years
Type: Full-time

Alexion

Skills & Focus: medical writing, regulatory compliance, clinical development, vendor management, project management, operational strategy, ICH/GCP guidelines, document development, team player, agile learner
About the Company: Alexion is a part of AstraZeneca and focuses on transforming the lives of people affected by rare diseases.
Experience: At least 5 -10 years of regulatory medical writing management and operational experience.
Type: Full-time

Eurofins Alphora

Skills & Focus: formulation development, process development, GMP production, oral dosage technologies, scale up, SOPs, batch records, troubleshoot, cGMP, project updates
About the Company: Eurofins Alphora is a global leader in pharmaceutical services and is known for its commitment to quality and compliance within drug development.

Profound Medical

Skills & Focus: assembly, testing, documentation, manufacturing, medical devices, quality compliance, cleanliness, inspection, ISO 9001, ISO 13485
About the Company: We are a group of energetic, problem-solvers focused on innovation and looking to change the world. We are changing the paradigm for treating diseases such as …
Experience: 1+ year of manufacturing experience in a regulated environment
Type: Full-Time

Astrazeneca

Skills & Focus: Regulatory Affairs, project management, drug development, biopharmaceutical, cross functional teams, risk management, submission strategy, process improvement, mentoring, compliance
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies dedicated to delivering life-changing medicines.
Experience: Extensive Regulatory experience (3+ years) within the biopharmaceutical industry, or at a Health Authority, or other proven experience.

Alexion

Skills & Focus: Quality Culture, Clinical Quality, GCP, Compliance, Regulatory, Mentoring, Coaching, Continuous Improvement, Risk Assessments, GxP Inspections
About the Company: At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the o…
Experience: 15+ years of experience in clinical research area inclusive of, but not limited to, Good Clinical Practice or Good Clinical Practice quality assurance and compliance.
Type: Full-time
Skills & Focus: Quality Culture, Stakeholder Management, GCP, Risk Management, Quality Management, Clinical Trials, Data Analysis, Inspection Readiness, Continuous Improvement, Compliance
About the Company: At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the o…
Experience: Minimum of 8+ years of experience in clinical research area inclusive of, but not limited to, Good Clinical Practice or Good Clinical Practice quality assurance and compliance.

Baxter

Skills & Focus: clinical knowledge, risk management, medical device, stakeholder collaboration, literature searches, training documents, evidence generation plan, safety documentation, ISO 14971, cross-functional partners
About the Company: At Baxter, we are deeply connected by our mission to save and sustain lives through medical innovations and products found in hospitals and homes globally.
Experience: At least 2 years of acute adult primary care, medical surgical, or related clinical experience work is required.
Benefits: Comprehensive benefits options reflecting the value placed in employees.

Jazz Pharmaceuticals

Skills & Focus: medical writing, regulatory documents, clinical trials, cross-functional teams, authoring, submission ready documents, ICH guidelines, Good Clinical Practices, document timelines, clinical development
About the Company: Jazz Pharmaceuticals is a global biopharma company dedicated to innovating and transforming the lives of patients with serious diseases. It has a diverse portf…
Experience: BA/BS with at least 6 years or advanced degree with at least 4 years writing experience in the pharmaceutical industry
Salary: $137,600.00 - $206,400.00
Type: Remote
Benefits: Discretionary annual cash bonus, equity grants, various benefits offerings

Eurofins Cdmo Alphora

Skills & Focus: Technology Transfer, cGMP, Manufacturing, Process Specialists, Master Batch Records, Compliance, Performance Management, Continuous Process Improvements, Clients Interaction, Training
Type: Full-time

Dana Incorporated

Skills & Focus: quality management, manufacturing environment, customer quality, corrective actions, quality systems, continuous improvement, leadership, regulatory compliance, statistical process control, project management
About the Company: Dana is a global leader in the supply of highly engineered driveline, sealing, and thermal-management technologies that improve the efficiency and performance …
Experience: Proven experience in quality management within a manufacturing environment.
Benefits: Competitive salary & benefits package, career growth opportunities in a dynamic manufacturing environment.

Eurofins Cdmo Alphora Inc.

Skills & Focus: Quality Assurance, cGMP, pharmaceutical, APIs, regulatory standards, SOPs, CAPAs, audits, quality control, continuous improvement
About the Company: Eurofins CDMO Alphora Inc. specializes in pharmaceutical contract development and manufacturing services.
Type: Full-time

Johnson & Johnson

Skills & Focus: Global Labeling, Regulatory Affairs, Labeling content, Pharmaceutical products, Compliance, Project management, Scientific communication, Continuous improvement, Healthcare innovation, Team leadership
About the Company: Johnson & Johnson is a global healthcare company, focused on innovating and improving health through their products and solutions.
Experience: A minimum of 8 years of professional work experience
Type: Hybrid

Universityhealthnetwork

Skills & Focus: quality assurance, dosimetry, treatment plans, linear accelerators, CT simulators, gamma knife, orthovoltage, radiation physics, QA procedures, research and development
Salary: $42.46 per hour - $53.08 per hour
Type: Permanent Full-Time

Johnson & Johnson

Skills & Focus: regulatory, medical writing, clinical documents, team environment, pharmaceutical, organization skills, problem-solving, scientific data, attention to detail, Microsoft Office
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Type: Remote
Benefits: We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority,…

Alimentiv-2

Skills & Focus: quality, compliance, auditor, regulatory, GxP, clinical research, risk-based auditing, adherence, standards, protocols

Johnson & Johnson

Skills & Focus: labeling, Regulatory Affairs, pharmaceutical, leading teams, scientific concepts, project management, document management systems, continuous improvement, communication skills, regulatory guidelines
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: A minimum of 8 years of professional work experience; A minimum of 6 years of direct regulatory labeling content experience.
Type: Hybrid
Skills & Focus: Regulatory, Medical Writing, Clinical Documents, Pharmaceutical, Protocols, Clinical Study Reports, Document QC, Scientific Discipline, Communication Skills, Project Management
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 2 years of relevant pharmaceutical/scientific experience
Type: Fully Remote
Benefits: We offer a competitive salary and extensive benefits package, a flexible working environment, and career development op…