Senior Manager Regulatory Affairs And Risk Management
By Enova Power Corp. At Kitchener, Ontario, Canada
Intermediate project management, time management and organizational skills
4 -10 years’ related experience and/or training or equivalent combination of education and experience
Advanced knowledge of the electricity regulated industry or equivalent experience with emphasis on rate design and cost allocation methodologies
Intermediate knowledge of Occupational Health and Safety requirements as it relates to individual, organizational and operational requirements
Senior Manager of Regulatory Affairs and Risk Management.
8 years’ experience in a supervisory role
Manager, Pharmaceutical Process Validation [Biovectra Inc. ]
By CareerBeacon At Charlottetown, Prince Edward Island, Canada
Qualification of new equipment/processes, computer-related system qualification and calibration program management.
Communicating and reporting the status of each project to the management and department that sponsors the project.
Ensuring that the Validation department meets budget provided by Senior Management.
Five years pharmaceutical industry experience.
Leading participant in conducting process risks analysis and process hazard analysis.
Developing, maintaining, and updating the Validation Master Plan (VPM) for the overall project.
Regulatory Affairs Manager Jobs
By BioMedica Diagnostics Inc. At Windsor, Nova Scotia, Canada
University Degree/Professional Designation or equivalent learning and experience in a related discipline (i.e. Management; RAC)
Effective communication with all stakeholders, including customers and government authorities. Abilities should include excellent presentation, writing, and editing skills.
Fundamental Skills, Abilities & Attributes
Manage and lead recalls vigilance procedures, health risk assessments.
Strong knowledge and understanding of cGMP, ISO 13485, MDSAP and IVDR guidelines, policies, and regulations
Technical knowledge of in-vitro diagnostic products
Regulatory Affairs Manager Jobs
By JAMP Pharma Group At Boucherville, Quebec, Canada
Experience in team and project management.
Manage safety updates to product monographs.
Maintain up-to-date knowledge of applicable company SOPs, guidelines, and work instructions as they relate to product labeling.
Understand the BPM audit process and requirements.
Minimum 3 years' experience (pharmaceutical industry, an asset).
Strong communication and negotiation skills.
Global Regulatory Affairs & Advisory Manager – Chemicals
By lululemon At Vancouver, British Columbia, Canada
Previous Project Management experience is an asset
Previous experience with the development and implementation of a Restricted Substances List or related chemicals management programs is an asset
In collaboration with the Chemicals Management Team, ensure regulated standards are reflected in annual updates to lululemon’s Restricted Substances List
Experience with national and/or international chemical laws and regulations applicable to adult apparel and accessories, , foods, electronics and equipment
Experience with regulatory, government and industry or standards organizations
Experience with legal and regulatory action is desired
Pharmaceutical Labeling Operations Manager - Regualtory - Remote
By ClinChoice At Canada
Effective leadership and team management abilities, with excellent communication and interpersonal skills.
Excellent project management skills, with the ability to prioritize tasks, manage timelines, and handle multiple projects simultaneously.
Strong knowledge of regulatory requirements and guidelines related to pharmaceutical labeling, including FDA, EMA, and ICH guidelines.
Familiarity with labeling software and tools, such as Labeling Management Systems (LMS), Adobe Illustrator, or similar applications.
Manage labeling artwork design, proofreading, and finalization processes to ensure error-free and high-quality labels.
Develop and implement labeling strategies, policies, and procedures to meet regulatory requirements and project timelines.
Regulatory Affairs Manager Jobs
By Canadian Hospital Specialties Limited At Oakville, Ontario, Canada
Develop and implement effective recall management procedures and processes.
Demonstrated leadership skills and experience in managing and mentoring a team.
Familiarity with quality management systems (e.g., MDSAP, QSR, GMP) and risk management (e.g., ISO 14971).
Quality Management System (QMS) Activities:
Ensure adherence to regulatory requirements throughout the product lifecycle.
Lead cross-functional teams in executing product recalls, ensuring compliance with regulatory requirements.
Pharmaceutical Regulatory Affairs Manager
By Collabera At Mississauga, Ontario, Canada
• Acts as a knowledgeable resource on limited topics to other Regulatory Affairs personnel within the department.
• Post-graduate certification in Regulatory Affairs is considered an asset.
• Experience in Virology or Oncology considered an asset
• Understanding and knowledge of the fundamentals of Canadian regulatory legislation and guidance.
• Excellent communication skills both in writing and verbally.
• Good judgment/ problem solving skills.