Food Safety and Compliance Specialist

About UsSteritech Brand Standards, a proud member of the Rentokil family in North America, stands as a global leader in pest control. With remarkable growth, we have doubled in size over the past five years. As the market leader in food safety, quality assurance, and customer experience management, we partner with some of the world's top brands across diverse sectors including manufacturing, processing, retail, food service, and hospitality. Our mission is to help our clients deliver the safest and healthiest services to their customers.Join Steritech – Your Career Growth AwaitsAt Steritech, we foster a culture of continuous learning and professional development. Many of our management team members began their careers with us as specialists, reflecting our commitment to promoting from within. When you join Steritech, you are not merely taking a job; you are embarking on a career path filled with opportunities for growth and advancement. We equip you with the tools, resources, and mentorship necessary for your success because your achievements contribute to our collective success. Become part of a team dedicated to your development, where your journey from specialist to leader can begin!Key Responsibilities of Our Food Safety and Compliance SpecialistsOur Food Safety and Compliance Specialists work closely with clients in the hotel, restaurant, and grocery sectors to uphold brand standards, ensure food quality, and deliver friendly service to customers. Responsibilities include:Conducting assessments to evaluate compliance with regulatory, industry, and proprietary brand standards.Monitoring food preparation and cooking standards to guarantee food safety, health, and sanitation practices.Collaborating with clients to identify the root causes of assessment discrepancies and formulating corrective action plans.Teaching and coaching clients on creating a safer and healthier workplace for themselves and their customers.Traveling up to 50% of the time, approximately 10 days per month, including some evenings and weekends.

About UsSteritech Brand Standards, a proud member of Rentokil, is North America's premier provider of pest control services. Over the last five years, we have doubled in size, establishing ourselves as the leading authority in food safety, quality assurance, and customer experience management. We are dedicated to aiding some of the world’s most reputable brands across various sectors, including manufacturing, processing, retail, food service, and hospitality, ensuring they deliver the safest and healthiest experiences to their customers.Grow Your Career with SteritechAt Steritech, we foster a culture that prioritizes continuous learning and professional development. Most of our management team members started their careers with us as specialists, which reflects our commitment to promoting from within and recognizing the potential of our team. By joining Steritech, you embark on a career path filled with opportunities for growth and advancement. We equip you with the tools, resources, and mentorship necessary for your success, as we believe your achievements are our achievements. Join a team committed to your development and where your journey from specialist to leader can begin!Role Overview: What Our Food Safety & Compliance Specialists DoOur Food Safety & Compliance Specialists play a vital role in assisting our hotel, restaurant, and grocery clients to uphold brand standards, ensure food quality, and deliver exceptional service. Their responsibilities include:Conducting assessments to evaluate compliance with established regulatory, industry, and proprietary brand standards.Monitoring food preparation and cooking standards to ensure adherence to food safety, health, and sanitation protocols.Collaborating with clients to identify root causes of assessment discrepancies and developing corrective action plans.Training and coaching clients to create a safer and healthier workplace for themselves and their customers.Traveling up to 50% of the time, approximately 10 days per month, which may include evenings and weekends.Qualifications: What You Need to SucceedTo thrive in this role, you should possess:Eligibility to obtain a CP-FS certification.A flexible work schedule from Sunday to Saturday to accommodate personal commitments.A willingness to travel by car and/or plane up to 50% of the time.The ability to lift up to 10 lbs to chest height, alongside skills in stooping, kneeling, crouching, and reaching.Outstanding listening and communication abilities.

As a Clinical Quality Manager at Abcellera, you will play a pivotal role in ensuring the highest standards of quality and compliance in our clinical processes. Your expertise will guide our teams in optimizing clinical operations, implementing quality assurance protocols, and leading continuous improvement initiatives.Join us in our mission to deliver innovative solutions that enhance patient care and clinical outcomes. We are looking for a leader who is passionate about quality management and thrives in a collaborative environment.

Join Our Team as a Medical Aesthetic Physician at Lougheed LaserPart-Time Position AvailableLougheed Laser is thrilled to offer an exceptional opportunity for a skilled Medical Aesthetic Physician to become a vital member of our dedicated team!As part of MedSpa Partners Inc., one of Canada's premier Medical Aesthetics clinic groups, we strive to deliver world-class patient experiences. Our mission is to empower our partners to achieve their personal and professional goals through a supportive and collaborative environment. Together with some of Canada’s most esteemed Medical Aesthetic Physicians, we are committed to innovation and excellence, driving the growth and success of the aesthetics industry in Canada.Our core values include: RESPECT, INNOVATION, COMMUNITY, EXCELLENCE, AGILITYWhat We Offer:Become part of an extensive network with leading Medical Aesthetics Physicians across Canada.Opportunities for training and professional growth.A robust marketing engine that supports and promotes your clinic.Access to cutting-edge research opportunities.Direct collaboration with top medical aesthetic physicians in Canada.

Join StackAdapt as a Quality Engineer, where you will play a crucial role in ensuring the delivery of high-quality software solutions. As part of our dynamic team, you will work closely with developers and product managers to identify and rectify issues, enhancing our product's reliability and user experience. You will be responsible for designing test plans, executing automated tests, and reporting on the software performance metrics. If you have a passion for quality and a keen eye for detail, we want to hear from you!

About Boomi and What Sets Us ApartAre you eager to join a dynamic and rapidly expanding company where your contributions truly matter? At Boomi, we strive to enhance global connectivity by linking everyone to everything, anywhere. Our award-winning, intelligent integration and automation platform empowers organizations to shape the future of business. Here, you'll collaborate with exceptional individuals and utilize cutting-edge technology. We seek innovators with an entrepreneurial mindset who excel at resolving complex challenges, making a tangible impact, and contributing to something monumental. For more insights, visit boomi.com or explore our Boomi Careers page.Your Impact at BoomiAs a Senior Software Quality Engineer, you'll integrate traditional software quality engineering practices with innovative AI quality methodologies. Your role will involve designing and implementing robust testing strategies to ensure the reliability of our backend infrastructure and the quality of the Generative AI features that power our intelligent applications. This position requires deep technical knowledge in automated testing and AI/ML-focused quality engineering, allowing you to establish quality benchmarks that encompass everything from microservices architecture to AI/ML models. You will play a crucial role in developing testing frameworks and quality processes that guarantee our products are resilient, dependable, and ready for deployment.

At Hiive, we are transforming the way private companies and their shareholders access liquidity. Our institutional-grade platform unites buyers, sellers, and issuers to facilitate secondary transactions in venture-backed, pre-IPO companies, enhancing efficiency, transparency, and standardization in an otherwise opaque asset class.As one of Canada’s fastest-growing companies, and backed by prominent U.S. investors, Hiive is profitable, well-capitalized, and actively building a high-performance team to meet increasing demand and explore new market opportunities.Curious about what it’s like to work at Hiive? Visit our careers page to discover how you can grow with us!In the role of Quality Assurance Engineer, you will play a vital role in ensuring that we deliver bug-free features on our platform. Collaborating with engineers and product managers, you will help ensure that the new features not only meet product objectives but are also free from bugs. Utilizing AI tools, you will enhance test coverage, speed up bug detection, and elevate overall QA efficiency. You will manage an end-to-end test suite using Playwright, verifying code prior to its production release. Your collaboration with peers will be crucial in improving test coverage, diagnosing bugs, and fostering an excellent and supportive engineering culture.Your responsibilities will include:Ensuring features are bug-free and align with product goals.Identifying and resolving potential issues proactively.Maintaining high product quality and ensuring a consistent and reliable user experience.Exhibiting exceptional attention to detail while designing and executing effective testing strategies.Utilizing AI-assisted tools to generate, maintain, and optimize automated test cases, thus improving test coverage.Employing AI to discover edge cases, analyze test results, and expedite root cause analysis of defects.Evaluating and integrating AI-driven QA tools and workflows to enhance testing efficiency and reliability.Collaborating closely with cross-functional teams to ensure the deployment of bug-free software.Assisting in coordinating the QA discipline at Hiive.

Role Overview AbCellera Biologics Inc. is hiring a Quality Control Systems Manager in Vancouver. This role focuses on strengthening quality management systems and ensuring compliance with industry standards and regulatory guidelines. What You Will Do Lead projects to align quality systems with current regulations and standards Work closely with teams across the company to implement quality management best practices Oversee quality assessments and audits Promote ongoing improvements in processes and systems

At AbCellera, we understand that the need for innovative medicines is paramount. Our mission is to consistently defy expectations by delivering groundbreaking therapies to patients who need them most. Driven by a commitment to scientific integrity and a willingness to explore the unknown, we are seeking a talented Medical Director to join our Clinical Development team, focusing on our oncology pipeline.In this pivotal role, you will lead the medical and scientific strategy for early oncology programs, guiding them from pre-IND/CTA stages through Phase 1 and 2. Your expertise will be essential in the design and execution of clinical studies, ensuring rigorous medical monitoring, and delivering insightful interpretations of clinical trial data while adhering to the highest standards of safety and regulatory compliance.

Role SummaryResponsibilities: Join our dynamic Health Economics team in our newly established Canadian office, where you will take a pivotal role in crafting health economic models across diverse disease areas. Leverage your expertise to deliver exceptional projects while nurturing client relationships. Additionally, you will contribute to business development initiatives and provide mentorship to junior team members as we enhance our presence and impact in Canada.Salary: A competitive starting salary ranging from CAD $95,000 to CAD $100,000 annually, commensurate with experience. Our established salary bands are based on educational attainment to ensure equity and consistency among all applicants, removing the need for individual negotiations.Benefits: Enjoy hybrid and flexible working arrangements, a generous vacation allowance, comprehensive private health and dental insurance, life insurance, a retirement savings plan, and full funding for external training along with study leave, among other perks.Role Type: This is a full-time, permanent position.Start Date: We are looking to fill positions with start dates throughout 2026, occurring monthly. Please indicate your availability in your application.Application Deadlines: While there are no fixed application deadlines, we encourage early applications as roles may close once suitable candidates are identified.Location: This opportunity is based in our brand-new office in Vancouver.About the RoleIf you possess a background in successfully conceptualizing, developing, and conveying health economic models that illustrate the value of innovative healthcare interventions within the Canadian context, we invite you to apply.

Role Overview AbCellera Biologics Inc. is hiring a Quality Control Systems Specialist in Vancouver. This role supports the integrity of quality control systems that underpin biopharmaceutical development. The position focuses on maintaining high standards and collaborating with teams across the organization to improve and implement quality management processes.

Join cima2 as a Quality Assurance Advisor specializing in Training & Development. In this pivotal role, you will ensure that our training programs meet the highest standards of quality and effectiveness. Collaborate with various departments to evaluate training needs, develop comprehensive evaluation strategies, and provide feedback to enhance program delivery.

At abcellera, we are driven by our commitment to improving patient outcomes through the development of innovative medicines. Our vision is to consistently overcome challenges to deliver transformative therapies to those in need. We embrace scientific integrity and have the courage to explore uncharted territories in our pursuit of truth.We are seeking an experienced and proactive Quality Control Manager to oversee the daily operations of our QC laboratory, with a strong emphasis on Microbiology. In this role, you will be pivotal in providing technical mentorship, addressing troubleshooting challenges, and ensuring compliance across various microbial methods, environmental monitoring (EM) programs, utilities monitoring, and contamination investigations. Your expertise will also contribute to broader QC functions, including stability studies, sample management, raw materials testing, and analytical assays such as UPLC, ELISA, and spectrophotometry.

Are you ready to embark on a rewarding journey with us? At JOEY Burrard, we value your passion, purpose, and potential. We recognize the qualities of care, drive, confidence, and curiosity that you bring to the table. Join our dynamic team where intensity, excitement, and energy are part of our culture. We are deeply committed to the continuous learning and growth of our staff, fostering an environment that nurtures talent.As a Food Expeditor, you will play a crucial role as the bridge between our Front of House and Back of House teams. Your mission will be to guarantee that every dish leaves our kitchen in a timely and consistent manner, reflecting our high standards for excellence. You will be responsible for ensuring that our guests enjoy world-class culinary experiences with every meal.

Role Overview The Vice President of Product at Spare leads the entire product function, shaping the direction and quality of our offerings. This is more than managing a roadmap, it means building a product operating system that ties together market research, customer feedback, AI capabilities, and company strategy to deliver products that make a measurable impact. Key Responsibilities Own the product strategy from planning through execution and delivery of outcomes Integrate market insights, customer needs, and AI technologies into product development Develop and refine operational frameworks for the product team Balance competing priorities to achieve business goals Collaborate as part of the senior leadership team, reporting directly to the co-founder and COO What We’re Looking For Proven experience leading product initiatives and building operational systems in similar settings Track record of making strategic decisions that drive business results Strong business mindset, focused on outcomes over features Hands-on experience applying AI in product development Ability to consistently raise product quality standards Location and Work Model This role is based at Spare’s Vancouver headquarters. The position follows a hybrid schedule, with in-office presence required on Monday, Wednesday, and Friday.

At AbCellera, we believe in the power of medicine to change lives. Our mission is to continuously overcome challenges to deliver innovative therapies to patients who need them most. We value truth, scientific rigor, and the courage to explore uncharted territories.We are looking for a highly skilled Medical Director to join our Clinical Development team. In this role, you will provide pivotal medical and scientific leadership for our pipeline programs focused on endocrinology and autoimmune diseases. You will oversee the entire clinical development process from pre-IND/CTA through Phase 1 and later-stage trials, leading cross-functional teams to develop and execute robust clinical strategies while ensuring compliance with safety and regulatory standards.

Role Overview AbbVie Inc. is seeking a Medical Science Liaison focused on solid tumours to support Western Canada. This field-based role centers on building scientific relationships with healthcare professionals and sharing up-to-date information on AbbVie’s therapies. What You Will Do Act as a scientific resource for oncology, specializing in solid tumour treatments. Engage with key opinion leaders and clinicians across Western Canada. Share clinical insights and support research initiatives related to AbbVie’s therapies. Contribute to projects that help advance patient care in oncology. What Sets This Role Apart This position offers the chance to make a direct impact on patient outcomes while working alongside colleagues who value scientific integrity and teamwork. AbbVie supports ongoing learning and collaboration as part of its commitment to advancing biopharmaceutical care.

Role Overview Benevity is hiring a Product Manager in Vancouver, British Columbia. This role focuses on shaping and improving Benevity’s product offerings. The Product Manager works closely with teams across the company to define product vision, collect requirements, and set priorities for new features that improve the user experience. What You Will Do Collaborate with cross-functional teams to set product direction Gather and document product requirements Prioritize features to drive user experience improvements Who Thrives Here This position suits someone who cares about building products that have a positive impact.

About UsAt Total Life, we are dedicated to transforming the later stages of life through growth, purpose, and emotional strength. Our mission is to combat the prevalent mental health challenges and anxiety faced by the elderly, making high-quality, affordable emotional support services accessible to a demographic often neglected in the digital health landscape.As a behavioral health company focused exclusively on individuals aged 65 and above, our core values are based on empathy, evidence-based care, and accessibility. We don’t merely provide therapy; we empower seniors to redefine their identities, manage complex health transitions, and sustain a high quality of life. By joining Total Life, you become part of a movement that ensures every senior has a dedicated partner in their mental health and wellness journey. Recognized as one of the Fortune 500 Top 5 Highest Growth Companies, we operate at an incredibly fast pace.Job OverviewWe are seeking a detail-oriented Medical Office Assistant to join our Vancouver office. In this role, you will serve as the operational backbone of our provider network, collaborating closely with the Provider Success Manager to meet the daily administrative and compliance needs of our US-based healthcare providers. Your responsibilities will encompass a variety of tasks—from onboarding and credentialing to systems management—ensuring our providers have the necessary tools to deliver exceptional care.

At Abcellera, we understand the importance of medicines in people's lives. Our mission is to consistently defy expectations to bring groundbreaking therapies to patients in need. We are committed to scientific integrity and embrace the challenge of navigating the unknown. We are seeking a dynamic and experienced Senior Quality Control Analyst to offer expert technical guidance in the daily operations of our Quality Control laboratory, primarily focusing on Microbiology. You will be a vital presence in the lab, providing troubleshooting expertise across microbial methodologies, environmental monitoring programs, utility assessments, and contamination investigations. Your daily responsibilities may include: Leading microbiological operations, including bioburden testing, endotoxin analysis, microbial identification, growth promotion assessments, environmental monitoring sampling, water testing, and result trending. Troubleshooting microbiological assays and contamination incidents, ensuring prompt and compliant resolutions. Offering in-lab mentorship to the QC team, promoting robust techniques, aseptic practices, and microbiological best practices. Maintaining inspection readiness of microbiology labs and adjacent QC spaces, ensuring compliance with GMP standards and equipment standard operating procedures. Coordinating stability sample retrievals, preparation, testing, and data tracking within QC programs. Overseeing sample receipt, chain-of-custody, aliquoting, storage conditions, and distribution workflows. Supporting routine sampling, testing, and trending of utilities (WFI, clean steam, compressed gases) along with appropriate documentation. Reviewing microbiological data packages, protocols, reports, and testing documentation for precision and adherence to ALCOA++ principles.