Senior Quality Control Analyst at Abcellera | Vancouver

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.

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.

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

Join AbCellera as a Clinical Study Manager, where your expertise will be pivotal in overseeing and managing clinical trials. You will collaborate with cross-functional teams to ensure the successful execution of studies that advance innovative therapies. Your role will involve developing study protocols, coordinating with stakeholders, and ensuring compliance with regulatory standards.

Join Abcellera as a Clinical Trial Coordinator, where you will play a crucial role in the management and execution of clinical trials. Your responsibilities will include coordinating trial activities, liaising with key stakeholders, and ensuring compliance with regulatory standards. The ideal candidate will have excellent organizational skills, attention to detail, and a passion for advancing medical science.

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.

At AbCellera, we believe in the power of medicine and the impact it can have on lives. Our mission is to consistently break barriers and deliver innovative therapies to patients who need them most. We are committed to scientific integrity and are unafraid to explore the unknown. We are seeking a highly skilled and strategically focused Principal Scientist to become a vital part of our Non-Clinical Safety team located in Vancouver, Canada. In this role, you will lead the design, planning, monitoring, and reporting of both non-GLP and GLP toxicology studies, providing essential nonclinical safety support for projects spanning early to late-stage development. Your daily responsibilities may include: Leading the strategic planning, design, execution, and interpretation of nonclinical toxicology programs to support IND, CTA, and BLA submissions, including general toxicity and reproductive and developmental studies, in accordance with global regulatory standards. Acting as the primary scientific liaison with contract research organizations (CROs), offering strategic oversight during protocol development, study execution, data analysis, and report finalization to ensure the timely, high-quality, and GLP-compliant completion of studies. Serving as an integral member of cross-functional discovery and development teams, contributing toxicology expertise to guide candidate selection, risk assessment, and program advancement. Providing critical scientific evaluations of toxicology data and clearly communicating risk-benefit assessments and recommendations to project teams and senior leadership, including implications for clinical development and regulatory strategies. Authoring and reviewing nonclinical safety sections of regulatory documents (INDs, CTAs, IBs, and BLAs), and serving as a subject matter expert during global regulatory interactions and health authority communications. Driving the development of integrated nonclinical safety strategies across AbCellera’s therapeutic portfolio, ensuring consistency, scientific rigor, and alignment with corporate objectives. Maintaining scientific leadership by staying updated on advances in toxicology science, methodologies, and evolving regulatory guidance, and translating these insights into best practices for internal programs.

At abcellera, we believe in the power of medicine to change lives. Our mission is to continually surpass expectations and deliver transformative therapies to patients in need. We are committed to pursuing scientific rigor and embracing the challenges that come with innovation. We are looking for a dedicated Clinical Supply Chain Manager to lead the comprehensive management of Investigational Medicinal Products (IMP) and supporting supplies for our global clinical trials. In this critical role, you will ensure that the right products are available at the right time and in optimal condition for our clinical studies and patients. Your strong collaboration skills will be essential as you work closely with cross-functional teams, including Clinical Operations, CMC, Quality Assurance, and Regulatory Affairs, while also overseeing external partners such as CMOs, depots, and couriers to implement effective clinical supply strategies. Key Responsibilities: Develop and maintain global supply plans for clinical trials, including demand forecasting across AbCellera’s projects. Oversee and maintain global inventory across all central depots and clinical sites to ensure a seamless supply chain, utilizing ERP/inventory systems for precise record-keeping. Manage packaging, labeling, and distribution activities in collaboration with CMO partners. Coordinate global shipments of clinical supplies in strict compliance with international trade regulations, import/export requirements, and customs documentation. Supervise and qualify temperature-controlled shipments (cold chain), partnering with Quality Assurance to address any temperature excursions. Work with teams and vendors to establish and lead User Acceptance Testing (UAT) for Interactive Response Technology (IRT/IXRS) systems that manage inventory, randomization, and drug assignment. Ensure all clinical supply activities comply with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and applicable global regulations. Act as the Clinical Supply Subject Matter Expert on clinical study teams, collaborating with CMC and Regulatory Affairs on label approvals and submission requirements. Oversee drug accountability, returns, and destruction processes, ensuring thorough documentation and assisting in the development and management of the clinical supply budget for assigned studies.

At Abcellera, we are driven by a passion for innovation and a commitment to making a meaningful impact in the fields of Protein Science, Drug Development, Manufacturing, and Quality. We are always on the lookout for exceptional talent to enhance our teams. If you have expertise in Translational Biology, Engineering, Bioinformatics, Machine Learning, IT, Laboratory Management, or Software Development, we want to hear from you.We receive a high volume of applications, and only those selected for interviews will be contacted. Please note that all communication from our Talent Discovery team will come from an @abcellera.com email address.

Role overview The QA Operations Manager at Abcellera leads quality assurance activities for operations in Vancouver. The main focus is on upholding and improving quality standards, ensuring compliance, and promoting quality throughout ongoing projects. Key responsibilities Oversee the rollout and maintenance of QA processes for operational teams Conduct audits to check compliance and evaluate performance Promote ongoing improvements in quality systems and practices Collaborate with cross-functional groups to support quality metrics and project objectives Collaboration This role works with teams throughout Abcellera, helping projects meet both internal quality standards and regulatory requirements.

As a Clinical Research Coordinator at Abcellera, you will play a pivotal role in managing and facilitating clinical trials. Your responsibilities will include coordinating day-to-day operations, ensuring compliance with regulatory requirements, and working closely with cross-functional teams to support the development of innovative therapeutic solutions.

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.

Join Abcellera as an In Vivo Technician II, where you will play a crucial role in advancing our innovative antibody discovery platform. You will work with a dynamic team of scientists and researchers to conduct in vivo studies that contribute to our mission of developing next-generation therapeutics. This position requires a keen attention to detail and a passion for scientific exploration.

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 Abcellera as the Associate Director of CMC Regulatory Affairs, where you will lead the regulatory strategy for our cutting-edge therapeutic products. In this pivotal role, you will work closely with cross-functional teams to ensure compliance with regulatory requirements and facilitate successful product development.Your expertise will guide the preparation and submission of regulatory documents, ensuring that our products meet the highest standards of safety and efficacy. You will play a key role in maintaining relationships with regulatory agencies and provide strategic insights to the development teams.

At AbCellera, we are driven by a shared commitment to improving the lives of patients in need of innovative therapies. Our mission is to consistently overcome challenges and deliver transformative medicines to those who require them. Embracing scientific rigor and a fearless approach to exploration, we work at the forefront of discovery. We are looking for a dedicated and detail-oriented In Vivo Specialist to join our dynamic team. In this pivotal role, you will leverage your extensive experience in conducting in vivo studies in alignment with Animal Use Protocols and Standard Operating Procedures. You will play a key part in the discovery of therapeutic antibodies and efficacy assessments, collaborating closely with fellow scientists and team members to address complex scientific challenges. Your daily responsibilities will include: Managing day-to-day study activities to ensure efficient and high-quality execution. Working collaboratively with study leads, scientists, and cross-functional teams to ensure compliance with study protocols and animal welfare standards. Providing technical support and troubleshooting, while identifying opportunities for workflow optimization and implementing best practices. Assisting in the preparation of Animal Use Protocols (AUPs) and Standard Operating Procedures (SOPs) to meet CCAC Regulations and Guidelines. Ensuring accurate data recording for all in vivo studies and assisting with data analysis as necessary. Training and mentoring team members to uphold safety policies, SOPs, and regulatory requirements. Conducting in vivo and ex vivo techniques to achieve study objectives using your technical expertise. Carrying out daily health assessments and clinical observations to maintain animal welfare and ensure meticulous documentation. Preparing and maintaining laboratory spaces, equipment, and consumables essential for in vivo and ex vivo work. Preparing and aliquoting reagents necessary for in vivo studies. You are an ideal candidate if you possess: A commitment to providing exceptional animal care while overseeing and conducting in vivo activities. Proficiency in animal handling, dosing (IV, IP, SQ), and blood collection, along with a solid understanding of the 3Rs and research ethics. At least 6 years of experience in an in vivo research environment; a BSc, MSc, or familiarity with in vitro and ex vivo techniques is a plus. The ability to manage competing priorities effectively in a fast-paced scientific environment.

At AbCellera, we are committed to the vision of delivering groundbreaking medicines to those in need. Our team embraces scientific rigor, truth, and the courage to explore the unknown. We are currently looking for a dedicated and detail-oriented In Vivo Specialist to join our innovative team in Vancouver. This role involves conducting in vivo studies in compliance with Animal Use Protocols and Standard Operating Procedures on either a Tuesday to Saturday or Sunday to Thursday work schedule.Your contributions will be vital to the discovery of therapeutic antibodies and their efficacy assessments. We value teamwork, innovation, and mutual support as we confront complex scientific challenges together.Daily Responsibilities:Executing in vivo and ex vivo techniques to fulfill study objectives, leveraging your expertise in in vivo procedures.Conducting daily health assessments and clinical observations to uphold the highest standards of animal welfare and ensure accurate record-keeping.Providing hands-on support during study activities to ensure efficient and high-quality execution.Maintaining laboratory spaces, equipment, and supplies necessary for in vivo and ex vivo work.Identifying and resolving technical challenges in real-time, while seeking opportunities to enhance procedures and workflow.Accurately documenting in vivo study data, adhering to stringent data integrity and documentation standards.Sharing technical insights and best practices with colleagues to promote compliance with SOPs, safety standards, and regulatory requirements.Collaborating closely with study managers and research teams to ensure alignment with study protocols and animal welfare considerations.

Join AbCellera as a Strategic Finance Intern for an immersive 8-month co-op/internship experience. In this role, you will support our finance team by analyzing data, preparing financial reports, and contributing to strategic projects that drive innovation in the biotech industry. This is an excellent opportunity for students passionate about finance and looking to gain hands-on experience in a dynamic environment.

Role Overview Kabam is looking for a Senior Quality Assurance Analyst to lead test planning and task verification for a dedicated team. This position works closely with both internal and external development partners to help maintain the quality of Kabam’s free-to-play gaming products. Location and Commitment Full-time, on-site position at the Downtown Vancouver studio Requires in-person attendance 5 days per week Temporary contract expected to last 8 months, ending December 2026 What You Will Do Own the test planning process for your team Verify tasks and ensure quality standards are met Work closely with development partners inside and outside the company Support the overall quality of Kabam’s gaming products

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!