--- title: 'Director, CMC Quality at AbCellera' canonical: 'https://feeny.ai/job/director-cmc-quality-abcellera-vancouver-jyhny6j1vscf' type: 'job' last_seen: '2026-10-23' --- # Director, CMC Quality at AbCellera - **Company:** AbCellera - **Location:** Vancouver, Canada - **Posted:** 2026-10-22 - **Last confirmed live:** 2026-10-23 - **Apply:** https://job-boards.greenhouse.io/abcellera/jobs/8042325003 ## Job description Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients who need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown. We are looking for an experienced Director, CMC Quality to serve as a technical quality expert for antibody products during clinical development all the way through post-commercialization. As a core member of the CMC team, you will provide quality leadership and serve as the single point of contact representing all quality functions for technical decisions, risks, and activities associated with the assigned products. This role requires deep technical and compliance expertise, strategic thinking, and cross-functional collaboration to ensure product quality, regulatory compliance, and lifecycle continuity are met and maintained. You’ll work closely with the Product and Analytical Development teams, Quality, Manufacturing, Supply Chain, Clinical and Regulatory teams, ultimately shaping how our antibody therapies reach patients. ## How you might spend your days - Serving as the senior Quality leader on the CMC core team to communicate product Quality strategy, deliverables, risks, and changes - Leading the CMC product Quality sub-team to define product quality strategy, priorities, and deliverables throughout the product lifecycle - Executing product strategy using strong quality and scientific knowledge, aligned with CMC development, technology transfers, and global regulatory filing strategies - Working cross-functionally to implement phase-appropriate control strategies, including starting materials, drug substance and drug product specifications, in-process controls, stability strategy, and product comparability strategies - Maintaining the Product Quality Risk Register  to identify, mitigate, and escalate issues related to manufacturing, analytical methods, or supply chain - Monitoring and reviewing cross-functional processes and product data to identify trends and ensure quality and compliance risks are proactively addressed and escalated, as needed - Interpreting and applying applicable regulatory guidelines and directives (e.g. 21CFR, EU GMP, USP,  Ph. Eur., and ICH) to product quality, staying abreast of changes and advising stakeholders appropriately - Assessing changes, deviations, and other events for product quality impact and ensure appropriate implementation plans are developed - Providing subject matter Quality expertise into the preparation and review of clinical and commercial regulatory submissions (e.g. IND/CTA/BLA/MAA), product-related responses to health authority questions, and during health authority inspections We’d love to hear from you if - You have a Bachelor’s degree in Life Sciences or Engineering (e.g., Biology, Biochemistry, Chemical Engineering), with an MS or PhD preferred, and 12+ years of biopharmaceutical experience in Quality, Regulatory, or Manufacturing Compliance, including CMC development and commercialization of products such as pre-filled syringes and autoinjectors; prior CMC Quality leadership experience is strongly preferred - You have a deep understanding of global cGMP regulations (Health Canada FDA, EMA, ICH) including phase-appropriate requirements for clinical vs. commercial products - You have demonstrated expertise in designing and executing product & process control and comparability strategies - You have excellent interpersonal and communications skills, with the ability to interface with a broad range of internal and external stakeholders at all levels of the organization - You have demonstrated strong leadership capability with ability to align on, make and act on decisions while balancing speed, quality, and risk - You are a detailed-oriented individual, highly organized, and thrive in collaborative and cross-functional fast-paced environments while managing multiple priorities ## What we offer AbCellera’s hiring range for this role is CAD $180,000 - $220,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, an annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship are a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials. ## About AbCellera Creating medicines is the most important work we can do. We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline. Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications. We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines. To apply Please submit your application through our website and refer to Job ID 23421 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address. ## About AbCellera ## Company Overview - **One-liner**: AbCellera is a clinical-stage biotechnology company that discovers and develops antibody-based medicines using an integrated platform from target identification through clinical manufacturing. - **Entity Type**: Public (Nasdaq: ABCL) - **Headquarters**: Vancouver, British Columbia, Canada - **Founded**: 2012 (based on “14+ Years” on corporate site) - **Founders**: Carl Hansen, PhD (Chairman, CEO & President); Véronique Lecault, PhD (Director, CTO) – originally six scientists from an academic lab ## Core Business - **Primary industry**: Biotechnology – antibody therapeutics - **Target customers**: B2B partnerships with biopharma companies (historically) and now also developing its own pipeline for patients - **Mission**: “To create a pipeline of innovative antibody medicines.” ## Products & Services - **Platform Technology**: A fully integrated antibody discovery and development platform combining microfluidics, single-cell analysis, computational biology, and protein engineering. Used to generate antibodies against complex targets (GPCRs, ion channels, multipass membrane proteins). - **ABCL635**: A first-in-class antibody for non-hormonal treatment of vasomotor symptoms (hot flashes) associated with menopause. Targets NK3R. Currently in Phase 1/2 clinical trial. - **ABCL575**: An investigational monoclonal antibody for moderate-to-severe atopic dermatitis, targeting OX40L with Fc-silencing and half-life extension. Phase 1 trial initiated Q3 2025. - **ABCL688**: An antibody medicine targeting a multipass complex membrane protein for an undisclosed autoimmune indication. Entered IND-enabling studies in Q2 2025. - **Partnership Business**: Completed 100+ discovery programs with 40+ partners since 2015, generating passive royalty stakes in partner drug programs. ## Market Standing - **Valuation/Market Cap**: Not publicly available from provided sources (public company; check Nasdaq: ABCL for current cap) - **Key Metric**: Public company with ~600 employees; 100+ programs delivered; internal pipeline moving into clinic - **Notable Investors/Partners**: Not specified in sources (as a public company, institutional investors are listed in SEC filings) - **Growth Signals**: Shift from pure partnership model to advancing internal pipeline; first internal program (ABCL635) reached Phase 1/2; new 130,000 sq ft GMP manufacturing facility in Vancouver; headcount growth from six scientists to ~600 ## Competitive Advantages - **Integrated platform** that covers the entire antibody development chain from target to clinical manufacturing, reducing handoffs and accelerating timelines. - **Proprietary microfluidics and single-cell analysis** technologies that enable high-throughput screening of natural immune responses. - **Deep expertise in difficult targets** (GPCRs, ion channels, multipass membrane proteins) that are challenging for traditional antibody discovery. - **Built over a decade of partnerships** – the platform was refined through 100+ partnered programs, creating a robust technology base. ## Strategic Focus - Transitioning from a technology-partnership company to a clinical-stage biotech advancing its own pipeline. - Prioritizing internal and co-development programs in endocrinology / women’s health, immunology & inflammation, and oncology. - Building in-house clinical manufacturing capabilities (CMC) to support GMP production of drug substance and drug product. ## Why Work Here - **Culture**: Values “truth and scientific rigor,” independent thinking, and courage to work at the edge of the unknown. - **Team focus areas**: Discovery, Data Science / ML / IT / Engineering, Clinical Manufacturing, Quality, and more. - **Perks & benefits**: - Comprehensive health benefits (medical, dental, life, critical illness) - Equity ownership (stock options/RSUs) - Retirement savings (RRSP/401K) with no employee match required (North America) - Minimum 3 weeks vacation plus 2 company-wide closures per year - Active lifestyle allowance - Immigration and relocation assistance - Personal & professional development (workshops, conferences) - World-class labs, offices, and on-site gym - **Work policy**: Likely on-site in Vancouver given lab and manufacturing roles; specific remote/hybrid options not detailed in provided sources. ## Sources 1. [abcellera.com](https://www.abcellera.com/) 2. [abcellera.com/about](https://www.abcellera.com/about) 3. [abcellera.com/careers](https://www.abcellera.com/careers) 4. [abcellera.com/current-openings](https://www.abcellera.com/current-openings) 5. 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