An experienced Strategy & Operations executive to turn years of leadership experience into meaningful coaching impact, working one-on-one with professionals to strengthen leadership capabilities and achieve career goals.
Compensation
Receive a fixed hourly rate for coaching services. Additional incentives: Access to selected bonuses linked to member engagement and community growth.
Responsibilities
Conduct one-on-one virtual coaching sessions
Guide professionals in improving management approach, communication, decision-making, problem-solving, and ability to lead teams effectively
Help members navigate organizational complexity, strategic priorities, operational challenges, business transformation, and leadership transitions
Help members define clear development objectives, monitor their progress, overcome obstacles, and maintain accountability
Communicate with members between coaching sessions through dedicated email and in-app messaging
Requirements
Nice to have: ICF-recognized coaching certification
The Staff Site Reliability Engineer will drive the reliability, security, and operational excellence of mission-critical cloud-native platforms supporting enterprise software solutions.
Compensation
Annual base salary ranging from CAD 140,000 to CAD 155,000.
Responsibilities
Drive site reliability engineering initiatives and operational excellence across mission-critical services running on AWS and Kubernetes.
Design, implement, and continuously improve deployment, release, and rollback strategies for complex distributed systems.
Build and maintain secure-by-default CI/CD pipelines with robust automation, governance, and policy-driven controls.
Improve platform observability through metrics, logging, distributed tracing, and actionable alerting.
Define, implement, and continuously mature Service Level Indicators (SLIs), Service Level Objectives (SLOs), and organization-wide reliability standards.
The Sr Officer, Content Development and Impact Reporting will play a key role in communicating the impact of philanthropic support and strengthening donor relationships. Working across Programs, Resource Mobilization, and Communications, you will transform program results and research into compelling, accessible, and audience-focused content.
Compensation
Annual compensation: CAD $66,100–$70,300.
Responsibilities
Lead the development of donor and foundation reports, managing the process from initial planning and information gathering through writing, editing, and final production.
Collaborate with program teams to collect relevant information and translate complex technical and programmatic results into clear, engaging, public-facing narratives.
Coordinate editing, proofreading, design reviews, and finalization of reports and donor stewardship materials.
Work closely with Philanthropy, Communications, and Programs teams to identify content needs, establish priorities, define key messages, and align materials with fundraising and stakeholder engagement objectives.
Research, write, and edit cases for support, issue briefs, backgrounders, and other fundraising and communications materials.
Requirements
Post-secondary degree or diploma in Communications, Journalism, English, International Development, Marketing, Public Relations, or a related discipline
As a Senior Executive Recruiter, you will play a key role in attracting and securing high-caliber talent to support business growth within the healthcare sector. This fully remote, temporary opportunity is suited to an experienced recruiter with deep healthcare industry knowledge and strong stakeholder management skills.
Compensation
Hourly compensation ranging from $45 to $55, depending on factors such as location, education, professional experience, certifications, and market conditions.
Responsibilities
Oversee end-to-end recruitment activities while acting as a trusted talent acquisition partner to hiring managers and business leaders
Partner with hiring managers to understand business needs, define recruitment priorities, and manage relationships throughout the hiring process
Provide consultative recruitment guidance, market insights, and recommendations to support effective hiring decisions
Develop and execute strategic, innovative sourcing and recruitment plans tailored to specific business areas and client groups
Build and maintain pipelines of diverse, highly qualified candidates through proactive sourcing and talent engagement strategies
Requirements
Bachelor's degree or higher
Nice to have: Experience recruiting in acute care and/or ambulatory healthcare environments
Nice to have: Previous experience working in a recruitment agency or executive search firm
Support regulatory affairs activities for small-molecule pharmaceutical products in a senior consulting role, ensuring compliance with North American regulatory requirements.
Responsibilities
Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.
Senior Regulatory CMC Consultant to support regulatory affairs activities for small-molecule pharmaceutical products, ensuring compliance with North American requirements.
Responsibilities
Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.
Support regulatory affairs activities for small-molecule pharmaceutical products in a senior consulting role, ensuring compliance with applicable North American requirements.
Responsibilities
Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.
Senior Regulatory CMC Consultant to support regulatory affairs activities for small-molecule pharmaceutical products, ensuring compliance with North American requirements.
Responsibilities
Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.
Experienced Regulatory CMC Consultant to support regulatory affairs activities for small-molecule pharmaceutical products, ensuring compliance throughout the product lifecycle.
Responsibilities
Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.
Requirements
Bachelor's degree
Master's degree
PhD degree
Nice to have: Small-molecule CMC regulatory activities
Seeking an experienced Regulatory CMC Consultant to support regulatory affairs activities for small-molecule pharmaceutical products in a senior consulting role.
Responsibilities
Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.
Requirements
Bachelor's degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or another life sciences discipline
Master's degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or another life sciences discipline
PhD degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or another life sciences discipline
Nice to have: Small-molecule CMC regulatory activities