Us Department Of Veterans Affairs Jobs overseas

About 6755 results in (3) seconds Clear Filters

Jobs Search

About 6755 results in (3) seconds
Executive Coordinator – Legal Affairs at Pomerleau
Montréal, QC H2Y 1S1, Canada - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Director, Medical Affairs, Tozorakimab at AstraZeneca
Wilmington, DE 19850, USA - Full Time
Skills Needed
Medicine, Management Skills, Communication Skills, Pipeline Management, Project Management Skills, Biologics, Pharmacology, Clinical Development
Qualification
Graduate
Experience Required
Minimum 2 year(s)
Associate Director, Regulatory Affairs at Piper Companies
Minneapolis, Minnesota, USA - Full Time
Skills Needed
Biologics, Strategy Execution, Pharmaceuticals, Regulatory Requirements, Communication Skills, Regulatory Affairs, Writing
Qualification
Phd
Experience Required
Minimum 7 year(s)
Regulatory Affairs CMC Senior Officer at Demo S.A.
Athens, Attica, Greece - Full Time
Skills Needed
Regulatory Strategy, Documentation Requirements, Cmc Documentation, Regulatory Submissions, Gmp Compliance, Ich Guidelines, Deficiency Letters, Cross Functional Collaboration, Communication Skills, Relationship Management, Organizational Skills, Multi Tasking, Deadline Management, Resilience, Ms Office Skills, Pharmaceutical Knowledge
Specialization
Candidates must have a BSc Degree in Chemistry, Pharmacy, Biology, or a relevant field, along with more than 3 years of experience in Regulatory Affairs/CMC. Knowledge of global regulatory guidelines and fluency in English are also required.
Experience Required
Minimum 5 year(s)
Principle Regulatory Affairs Associate at Apple
Beijing, Beijing, China - Full Time
Skills Needed
Regulatory Affairs, Medical Device, Communication Skills, Problem Solving, Team Collaboration, Autonomy, Influencing Decisions, Wearable Technology, Samd Product, Judgment, Engagement Strategy, Health Space, Innovation, Relationship Building, Quality Assurance, Chinese Language
Specialization
A Bachelor's degree in science or engineering is required along with 7+ years of experience in regulatory affairs. Fluency in both English and Chinese is essential.
Experience Required
Minimum 10 year(s)
Country Head, Medical Affairs - Canada at Seqirus Canada
Quebec City, QC, Canada - Full Time
Skills Needed
Design, Clinical Development, Pharmacovigilance, Regulatory Affairs, Strategy, Publication Planning, Research, Vaccines, Strategic Initiatives, Collaboration, Scientific Communications, Regulatory Agencies, Publications, Timelines, Oversight
Qualification
Graduate
Experience Required
Minimum 10 year(s)
Regularoty Affairs & Quality Executive at Ascensia Diabetes Care
Singapore, , Singapore - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Corporate Director, Regulatory Affairs at Emory Healthcare
Tucker, Georgia, United States - Full Time
Skills Needed
Regulatory Affairs, Healthcare Quality, Leadership, Communication, Collaboration, Compliance, Patient Safety, Quality Improvement, Survey Management, Policy Development, Training, Data Analysis, Crisis Management, Accreditation Standards, Operational Strategies, Mentorship
Specialization
Candidates must have a Master's Degree in a relevant field and at least 10 years of experience in regulatory affairs or healthcare quality, with 5 years in a leadership role. A deep understanding of healthcare regulations and exceptional leadership skills are essential.
Experience Required
Minimum 10 year(s)
Public Affairs Manager, North America at ARRIVE
Atlanta, GA 30309, USA - Full Time
Skills Needed
Good Communication Skills
Specialization
Political science public policy business or a related field
Qualification
Graduate
Senior Specialist, Regulatory Affairs at West Pharmaceutical Services
Dublin, County Dublin, Ireland - Full Time
Skills Needed
Combination Products, Iso, Powerpoint, Dmf, Deliverables, Design, Specifications, Decision Making, Technical Reports, Preparation, Technical Standards, Regulations, Excel, Adobe Acrobat, Documentation, Confidentiality, Color, Medical Devices, Product Requirements
Specialization
Science math engineering or related discipline required or
Qualification
Graduate
Experience Required
Minimum 3 year(s)
Manager, Rates and Regulatory Affairs at Liberty
Fall River, MA 02720, USA - Full Time
Skills Needed
Availability, Completion
Qualification
Graduate
Experience Required
Minimum 10 year(s)
Regulatory Affairs Specialist (m/w/d) at ARC Laser GmbH
90411 Nürnberg, , Germany - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Director of Global Regulatory Affairs at Danaher - Canada
Munsons Corners, Maryland, United States - Full Time
Skills Needed
Regulatory Compliance, Quality Assurance, Iso 9001, As9100, Gmp, Fda Knowledge, Product Compliance, Environmental Compliance, Airworthiness, Engineering, Product Lifecycle, Continuous Improvement, Auditing, Documentation, Problem Solving, Collaboration, Negotiation
Specialization
A BS/BA is required, preferably in engineering or a related field, along with 15 years of progressive experience in regulatory compliance or quality assurance. Candidates should have a thorough understanding of relevant standards and regulatory requirements.
Experience Required
Minimum 10 year(s)
Quality and Regulatory Affairs Manager at medmix
Kiel, Schleswig-Holstein, Germany - Full Time
Skills Needed
Qualitätsmanagement, Regulatory Affairs, Iso 13485, Mdr, Fda, Projektmanagement, Technische Dokumentation, Qm Systeme, Schulung, Lieferantenmanagement, Ms Office, Sap, Deutsch, Englisch
Specialization
A successfully completed technical or scientific degree, preferably in medical technology or a comparable field is required. Extensive professional experience in quality management in the regulated manufacturing industry, particularly in medical technology or pharmaceuticals, is essential.
Experience Required
Minimum 10 year(s)
ANZ Regulatory Affairs Lead Specialist at GE HealthCare Technologies
Mascot NSW 2020, , Australia - Full Time
Skills Needed
Project Management Skills, Communication Skills, Regulatory Affairs
Qualification
Diploma
Regulatory Affairs Specialist (m/w/d) at ABAX Personaldienstleistungen GmbH
LAR, , Germany - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Senior Manager, CMC Regulatory Affairs at Spyre Therapeutics
Remote, Oregon, USA - Full Time
Skills Needed
Good Communication Skills
Specialization
Cmc regulatory affairs including experience with clinical biologics programs or equivalent related experience
Qualification
Graduate
Senior Manager, Global Medical Affairs at Theramex
London SW1H, , United Kingdom - Full Time
Skills Needed
Pharmaceutical Industry, Materials, Strategic Thinking, Clinical Research, Pharmacovigilance, Leadership Skills
Qualification
Graduate
Praktikant (m/f/x) Regulatory Affairs at HYDROGENIOUS LOHC TECHNOLOGIES GmbH
91058 Erlangen, , Germany - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Regulatory Affairs in Clinical Trials at PSI CRO
Ciudad de México, , Mexico - Full Time
Skills Needed
Regulatory Affairs, Clinical Trials, Communication, Collaboration, Problem Solving, Detail Oriented, Ms Office, Safety Reporting, Training, Project Management, Research, Documentation, Ethics Submissions, Feasibility Research, Teamwork, English Proficiency
Specialization
A college/university degree in Pharmacy, Medicine, Life Sciences, or equivalent is required along with prior experience in clinical trial submissions. Full working proficiency in English and proficiency in MS Office applications are also necessary.
Experience Required
Minimum 2 year(s)
Executive Coordinator – Legal Affairs at Pomerleau
Montréal, QC H2Y 1S1, Canada -
Full Time


Start Date

Immediate

Expiry Date

13 Dec, 25

Salary

0.0

Posted On

16 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Human Resources/HR

Description

GENERAL INFORMATION

Job Location
Montreal, QC
Date Published
11-Sep-2025
Department
Compliance & Legal
Employment Type
Permanent
Working Arrangement
Hybrid
Role Type
Full-Time

JOB DESCRIPTION

Ready to build your career? We want to hear from you.
Reporting to the Executive Vice President and Chief Legal Officer, you will have the opportunity to take on significant and diverse responsibilities that will allow you to fully leverage your potential.

What you will do

  • Organize and plan the agenda for the project approval committee.
  • Ensure the execution of various mandates across different departments.
  • Draft various types of documents (agendas, email messages, meeting minutes, etc.).
  • Act as the main point of contact for the Executive Vice President, delegate requests, and facilitate the execution of her responsibilities.
  • Schedule various meetings, including preparing necessary documents and/or PowerPoint presentations.
  • Organize and structure documents intended for board members, ensuring their quality, compliance, and secure distribution.
  • Collaborate in coordinating and tracking the steps of the gating process, ensuring liaison with decision-making bodies and internal stakeholders.
  • Contribute to the structuring of required documents, planning of meetings, and tracking of associated deliverables.
  • Ensure proactive management of the calendar and travel arrangements.
  • Responsible for managing emails by establishing an efficient and organized filing system.
  • Ensure task follow-up and prioritization, as well as the quality of existing processes.
  • Translate various departmental communications.
  • Present information in a structured manner as shared by various stakeholders and/or members of the leadership team, notably through PowerPoint presentations.
  • Ensure smooth logistical operations, when applicable: making sure any logistical issues (IT, equipment, etc.) are resolved.
  • Provide high-quality customer service, both verbally and in writing.

This role could be for you if you have

  • 5 years of relevant experience in administrative support within corporate governance and/or internal committee management.
  • Advanced knowledge of Microsoft Office Suite (Word, Excel, Visio, PowerPoint, and Outlook).
  • Knowledge of Diligent Board (an asset).
  • Demonstrates discretion and confidentiality.
  • Anticipate needs and/or requirements.

Benefits

  • RRSP with up to 5% employer matching
  • Hybrid work model for corporate roles
  • Employee stock ownership program
  • Career growth through real development opportunities
  • Transit pass reimbursement — get to work for free
  • Minimum 4 weeks of vacation from day one

For the past four years, we’ve proudly held the distinction of being one of Canada’s Top 100 Employers.
Pomerleau is a national leader in construction, delivering major projects across Canada. We believe in creating a workplace where people feel respected, supported, and empowered to grow. Our culture is built on collaboration, trust, and a shared commitment to doing great work. If this speaks to you, apply for this role or connect with one of our recruiters to learn how we can support you throughout the process

Responsibilities

What you will do

  • Organize and plan the agenda for the project approval committee.
  • Ensure the execution of various mandates across different departments.
  • Draft various types of documents (agendas, email messages, meeting minutes, etc.).
  • Act as the main point of contact for the Executive Vice President, delegate requests, and facilitate the execution of her responsibilities.
  • Schedule various meetings, including preparing necessary documents and/or PowerPoint presentations.
  • Organize and structure documents intended for board members, ensuring their quality, compliance, and secure distribution.
  • Collaborate in coordinating and tracking the steps of the gating process, ensuring liaison with decision-making bodies and internal stakeholders.
  • Contribute to the structuring of required documents, planning of meetings, and tracking of associated deliverables.
  • Ensure proactive management of the calendar and travel arrangements.
  • Responsible for managing emails by establishing an efficient and organized filing system.
  • Ensure task follow-up and prioritization, as well as the quality of existing processes.
  • Translate various departmental communications.
  • Present information in a structured manner as shared by various stakeholders and/or members of the leadership team, notably through PowerPoint presentations.
  • Ensure smooth logistical operations, when applicable: making sure any logistical issues (IT, equipment, etc.) are resolved.
  • Provide high-quality customer service, both verbally and in writing

This role could be for you if you have

  • 5 years of relevant experience in administrative support within corporate governance and/or internal committee management.
  • Advanced knowledge of Microsoft Office Suite (Word, Excel, Visio, PowerPoint, and Outlook).
  • Knowledge of Diligent Board (an asset).
  • Demonstrates discretion and confidentiality.
  • Anticipate needs and/or requirements
Executive Coordinator – Legal Affairs at Pomerleau
Montréal, QC H2Y 1S1, Canada - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Director, Medical Affairs, Tozorakimab at AstraZeneca
Wilmington, DE 19850, USA - Full Time
Skills Needed
Medicine, Management Skills, Communication Skills, Pipeline Management, Project Management Skills, Biologics, Pharmacology, Clinical Development
Qualification
Graduate
Experience Required
Minimum 2 year(s)
Associate Director, Regulatory Affairs at Piper Companies
Minneapolis, Minnesota, USA - Full Time
Skills Needed
Biologics, Strategy Execution, Pharmaceuticals, Regulatory Requirements, Communication Skills, Regulatory Affairs, Writing
Qualification
Phd
Experience Required
Minimum 7 year(s)
Regulatory Affairs CMC Senior Officer at Demo S.A.
Athens, Attica, Greece - Full Time
Skills Needed
Regulatory Strategy, Documentation Requirements, Cmc Documentation, Regulatory Submissions, Gmp Compliance, Ich Guidelines, Deficiency Letters, Cross Functional Collaboration, Communication Skills, Relationship Management, Organizational Skills, Multi Tasking, Deadline Management, Resilience, Ms Office Skills, Pharmaceutical Knowledge
Specialization
Candidates must have a BSc Degree in Chemistry, Pharmacy, Biology, or a relevant field, along with more than 3 years of experience in Regulatory Affairs/CMC. Knowledge of global regulatory guidelines and fluency in English are also required.
Experience Required
Minimum 5 year(s)
Principle Regulatory Affairs Associate at Apple
Beijing, Beijing, China - Full Time
Skills Needed
Regulatory Affairs, Medical Device, Communication Skills, Problem Solving, Team Collaboration, Autonomy, Influencing Decisions, Wearable Technology, Samd Product, Judgment, Engagement Strategy, Health Space, Innovation, Relationship Building, Quality Assurance, Chinese Language
Specialization
A Bachelor's degree in science or engineering is required along with 7+ years of experience in regulatory affairs. Fluency in both English and Chinese is essential.
Experience Required
Minimum 10 year(s)
Country Head, Medical Affairs - Canada at Seqirus Canada
Quebec City, QC, Canada - Full Time
Skills Needed
Design, Clinical Development, Pharmacovigilance, Regulatory Affairs, Strategy, Publication Planning, Research, Vaccines, Strategic Initiatives, Collaboration, Scientific Communications, Regulatory Agencies, Publications, Timelines, Oversight
Qualification
Graduate
Experience Required
Minimum 10 year(s)
Regularoty Affairs & Quality Executive at Ascensia Diabetes Care
Singapore, , Singapore - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Corporate Director, Regulatory Affairs at Emory Healthcare
Tucker, Georgia, United States - Full Time
Skills Needed
Regulatory Affairs, Healthcare Quality, Leadership, Communication, Collaboration, Compliance, Patient Safety, Quality Improvement, Survey Management, Policy Development, Training, Data Analysis, Crisis Management, Accreditation Standards, Operational Strategies, Mentorship
Specialization
Candidates must have a Master's Degree in a relevant field and at least 10 years of experience in regulatory affairs or healthcare quality, with 5 years in a leadership role. A deep understanding of healthcare regulations and exceptional leadership skills are essential.
Experience Required
Minimum 10 year(s)
Public Affairs Manager, North America at ARRIVE
Atlanta, GA 30309, USA - Full Time
Skills Needed
Good Communication Skills
Specialization
Political science public policy business or a related field
Qualification
Graduate
Senior Specialist, Regulatory Affairs at West Pharmaceutical Services
Dublin, County Dublin, Ireland - Full Time
Skills Needed
Combination Products, Iso, Powerpoint, Dmf, Deliverables, Design, Specifications, Decision Making, Technical Reports, Preparation, Technical Standards, Regulations, Excel, Adobe Acrobat, Documentation, Confidentiality, Color, Medical Devices, Product Requirements
Specialization
Science math engineering or related discipline required or
Qualification
Graduate
Experience Required
Minimum 3 year(s)
Manager, Rates and Regulatory Affairs at Liberty
Fall River, MA 02720, USA - Full Time
Skills Needed
Availability, Completion
Qualification
Graduate
Experience Required
Minimum 10 year(s)
Regulatory Affairs Specialist (m/w/d) at ARC Laser GmbH
90411 Nürnberg, , Germany - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Director of Global Regulatory Affairs at Danaher - Canada
Munsons Corners, Maryland, United States - Full Time
Skills Needed
Regulatory Compliance, Quality Assurance, Iso 9001, As9100, Gmp, Fda Knowledge, Product Compliance, Environmental Compliance, Airworthiness, Engineering, Product Lifecycle, Continuous Improvement, Auditing, Documentation, Problem Solving, Collaboration, Negotiation
Specialization
A BS/BA is required, preferably in engineering or a related field, along with 15 years of progressive experience in regulatory compliance or quality assurance. Candidates should have a thorough understanding of relevant standards and regulatory requirements.
Experience Required
Minimum 10 year(s)
Quality and Regulatory Affairs Manager at medmix
Kiel, Schleswig-Holstein, Germany - Full Time
Skills Needed
Qualitätsmanagement, Regulatory Affairs, Iso 13485, Mdr, Fda, Projektmanagement, Technische Dokumentation, Qm Systeme, Schulung, Lieferantenmanagement, Ms Office, Sap, Deutsch, Englisch
Specialization
A successfully completed technical or scientific degree, preferably in medical technology or a comparable field is required. Extensive professional experience in quality management in the regulated manufacturing industry, particularly in medical technology or pharmaceuticals, is essential.
Experience Required
Minimum 10 year(s)
ANZ Regulatory Affairs Lead Specialist at GE HealthCare Technologies
Mascot NSW 2020, , Australia - Full Time
Skills Needed
Project Management Skills, Communication Skills, Regulatory Affairs
Qualification
Diploma
Regulatory Affairs Specialist (m/w/d) at ABAX Personaldienstleistungen GmbH
LAR, , Germany - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Senior Manager, CMC Regulatory Affairs at Spyre Therapeutics
Remote, Oregon, USA - Full Time
Skills Needed
Good Communication Skills
Specialization
Cmc regulatory affairs including experience with clinical biologics programs or equivalent related experience
Qualification
Graduate
Senior Manager, Global Medical Affairs at Theramex
London SW1H, , United Kingdom - Full Time
Skills Needed
Pharmaceutical Industry, Materials, Strategic Thinking, Clinical Research, Pharmacovigilance, Leadership Skills
Qualification
Graduate
Praktikant (m/f/x) Regulatory Affairs at HYDROGENIOUS LOHC TECHNOLOGIES GmbH
91058 Erlangen, , Germany - Full Time
Skills Needed
Good Communication Skills
Qualification
Graduate
Regulatory Affairs in Clinical Trials at PSI CRO
Ciudad de México, , Mexico - Full Time
Skills Needed
Regulatory Affairs, Clinical Trials, Communication, Collaboration, Problem Solving, Detail Oriented, Ms Office, Safety Reporting, Training, Project Management, Research, Documentation, Ethics Submissions, Feasibility Research, Teamwork, English Proficiency
Specialization
A college/university degree in Pharmacy, Medicine, Life Sciences, or equivalent is required along with prior experience in clinical trial submissions. Full working proficiency in English and proficiency in MS Office applications are also necessary.
Experience Required
Minimum 2 year(s)
Loading...