Senior Specialist, Operations Quality

Work Flexibility: Hybrid Senior Specialist, Operations Quality This position is responsible for providing dedicated support to Operations to develop and maintain those areas of the quality management system in accordance with ISO standards, Good Manufacturing Practices (GMP), Stryker Corporate requirements, and Canadian regulatory requirements. This individual is responsible to support and ensure that effective and efficient quality practices are maintained in collaboration with Global Logistics & Operations (GLO). This individual must serve as a contributing member of the Quality Assurance team while championing Stryker’s Mission and Values. Responsibilities: Individual Responsibilities: Proactively collaborates with internal and external stakeholders to promote a culture of inclusiveness and cooperation Responsible to live and exemplify Stryker’s Values: Integrity, Accountability, People, and Performance Functional Responsibilities: Act as the key contact for Quality related activities within Operations for Stryker Canada Identify improvements and inputs into the quality planning process Represent QA and act as the QA stakeholder on Operations-led projects Responsible for the review of programs and/or processes impacting the Quality Management System governing the distribution of regulated products within Canada Identify and implement improvement opportunities to increase the efficiency and effectiveness of QMS related documents for Operations Ensure quality records are established and maintained to provide evidence that the QMS is being followed Implement and maintain the Validation Program in collaboration with Operations and GLO for Stryker Canada Provide oversight for the development and/or execution of plans, protocols, reporting, training and quality system documents associated with validation requirements Responsible for the support and review of NCs and CAPAs for Operations, with attention to detail, review for completeness of actions and records, accuracy, and effectivity, and timelines Facilitate Operations teams in the application of problem-solving techniques and promote its uses and development (e.g. 5 Why's, fishbone diagrams, 4D’s, process mapping, etc.) Support the creation of quality objectives/KPI’s for Operations, and provide support in meeting requirements/targets Drive Good Manufacturing Practices and Good Documentation Practices within Operations Other duties as assigned by Manager Conduct & Compliance Abide by and support the policies set forth in the Stryker Code of Conduct Understand that compliance with the Code of Conduct, as it may be amended by Stryker Corporation from time to time, is a condition of continued employment with Stryker Conduct work in compliance with all laws, rules, and regulations and in accordance with Stryker’s high ethical standards Report any violations of these policies and procedures to Stryker management or in the manner outlined in Stryker’s Ethics Hotline Policy Knowledge & Skill Requirements Working knowledge of ISO 9001 requirements Working knowledge of Canadian regulations for medical devices, CTO (cells, tissues, and organs), drugs, natural health products, and cosmetics Strong computer skills (Excel, Word, Power Point, SharePoint), Trackwise and ComplianceWire will be considered an asset High standard of integrity and ability to meet deadlines Highly organized and able to prioritize tasks Project management and report writing; preferable Strong oral and written communication skills with both internal and external contacts Education & Qualifications University degree in Science, Engineering or related field required Post-graduate diploma in Regulatory Affairs or Quality Assurance preferred Minimum 3+ years’ experience in regulatory affairs and/or quality assurance Medical Device and/or Pharmaceutical experience is an asset Internal applicants with an equivalent combination of education, experience and performance over time at Stryker will be considered Canada Pay Ranges: Canada: $72,400 - $96,600 CAD Annual Travel Percentage: None

The Senior Specialist is responsible for supporting Operations in developing and maintaining the Quality Management System in compliance with ISO, GMP, and Canadian regulatory standards. They act as the primary QA stakeholder for Operations projects, overseeing validation programs, CAPA processes, and quality record maintenance.

Candidates must hold a university degree in Science, Engineering, or a related field, with a preference for a post-graduate diploma in Regulatory Affairs or Quality Assurance. A minimum of 3 years of experience in regulatory affairs or quality assurance within the medical device or pharmaceutical industry is required.

• Problem solvingPreferred
• Data analysisPreferred
• Project managementPreferred

Identified from the job description. Confirm important requirements above.

• Quality Management System
• ISO 9001
• Good Manufacturing Practices
• Regulatory Affairs
• Validation Program
• CAPA
• Problem-solving
• Process mapping
• KPI development
• Project management
• Report writing
• Compliance
• Data analysis
• Technical documentation
• Stakeholder management
• Report Writing
• TrackWise
• Good Documentation Practices
• Global Logistics
• Accountability
• Process Mapping
• Ability To Meet Deadlines
• Ethical Standards And Conduct
• Medical Devices
• Planning
• Microsoft Excel
• Quality Management Systems
• ISO 9000 Series
• Management
• Corrective And Preventive Action (CAPA)
• Communication
• Computer Literacy
• Cooperation
• Problem Solving
• Key Performance Indicators (KPIs)
• Project Management
• Operations
• Pharmaceuticals
• Microsoft PowerPoint
• Quality Assurance
• Safety Assurance
• Microsoft SharePoint
• ISO/IEC Standards
• Detail Oriented

• Healthcare
• Manufacturing
• Logistics
• Science & Research
• Engineering
• Quality Operations Manager
• Scheduler / Operations Coordinator
• Stock Clerks
• Production, Planning, and Expediting Clerks

Minimum education

Bachelor’s degree

Minimum experience

3+ years

Posting language

English

Working hours

40 hours per week