Find work in Canada.

324,917 jobs across our Canadian network. How we count

Jobs in Canada

25+ jobs

Email me new jobs Save this search

Added 5 mins ago
F/
DevOps Developer (Platform Engineering)
FCC / FAC
Regina, SK
- Full-time
As a DevOps Developer on our Platform Engineering team, you'll design, build, automate and support the cloud platforms and infrastructure that power enterprise technology across the…
Added 5 mins ago
SI
Senior Developer
SAP IT Business Systeme
Montreal, QC
- $108,100 to $222,800 CAD / year
- Full-time
We are looking for a dynamic and motivated Senior Software Developer who embrace AI-assisted software development as part of their everyday engineering practice to join our engineering…
Added 5 mins ago
SI
Software Developer
SAP IT Business Systeme
Montreal, QC
- $77,500 to $166,200 CAD / year
- Full-time
We are looking for a dynamic and motivated Software Developer who embrace AI-assisted software development as part of their everyday engineering practice to join our engineering team. The…
Added 5 mins ago
Software Developer
AppDirect
Toronto, ON
Added 5 mins ago
MI
Maker, Tool & Die (Certified)
Magna International
Markham, ON
- Full-time
…Powertrain, and we do it by creating world-class powertrain systems. We are a premier supplier for the global automotive industry with full capabilities in design, development, testing and…
Added 5 mins ago
T&
Project Coordinator/Administrator
Turner & Townsend
Toronto, ON
- Full-time
Experience with document management workflows, activity tracking systems, and visual reporting tools.
Added 5 mins ago
MC
Financial Services Representative - Full Time (Vineland Branch)
Meridian Credit Union
Vineland, ON
- $50,000 to $53,000 CAD / year
- Full-time
Added 5 mins ago
Low-Level Software Engineer, LLK
Tenstorrent
Toronto, ON
Strong problem solver who can investigate complex performance and systems challenges and drive them to resolution.
Added 5 mins ago
GT
Analyst, Business Planning and Analysis
Greater Toronto Airports Authority
Toronto, ON
- Full-time
…operating expenditure variances; gathering data from Finance tools, systems, and other sources; compiling and analyzing reports on business unit financial performance; identifying reporting…
Added 5 mins ago
GT
Senior Specialist, Procurement Governance
Greater Toronto Airports Authority
Toronto, ON
- Full-time
Experience with SharePoint, document management systems, Microsoft Power Platform, Power BI, workflow automation, or enterprise systems.
Added 5 mins ago
GT
Specialist, Procurement Governance
Greater Toronto Airports Authority
Toronto, ON
- Full-time
Experience with enterprise systems, reporting tools, and workflow automation technologies is considered an asset.
Added 5 mins ago
AF
Sales Associate
Anytime Fitness - 567508
Okotoks, AB
- $15 CAD / hour
- Part-time
Comfortable working with technology (CRM systems, email, etc.)
Added 5 mins ago
TT
Dispatcher
Trimac Transportation
Edmonton, AB
- Full-time
Added 5 mins ago
R(
Store Manager - Smart Centres Mount Pearl
Reitmans (Canada) Ltée/Ltd
Mount Pearl, NL
- Full-time
Proficient in POS, ERP, ATS systems and Microsoft Office Suite.
Added 5 mins ago
M(
Full-Stack Developer - Platform & Infrastructure
MaintainX (An Autodesk Company)
Remote, Canada
- Full-time
- Remote
…with search technology, authentication and identity, design systems or component libraries, developer tooling or IDE extensions, CI/CD, observability, or compliance programs such as FedRAMP…
Added 5 mins ago
M(
Full-Stack Developer - Core
MaintainX (An Autodesk Company)
Remote, Canada
- Full-time
- Remote
Strong written and verbal communication: you can explain a technical tradeoff to a designer or a support lead as easily as to another developer.
Added 5 mins ago
DC
Civil Engineering Technologist
Dillon Consulting Limited
Calgary, AB · Edmonton, AB
- Full-time
…connected, including water mains, sanitary sewers, stormwater systems, and…
Added 5 mins ago
DC
Civil Engineering Technologist
Dillon Consulting Limited
Calgary, AB · Edmonton, AB
- Full-time
…connected, including water mains, sanitary sewers, stormwater systems, and…
Added 5 mins ago
DC
Civil Engineer
Dillon Consulting Limited
Fredericton, NB
- Full-time
Experienced in the design of various municipal infrastructure including water supply systems, sewage systems, roadways, storm water management works, underground and surface site servicing…
Added 5 mins ago
DC
Civil Engineering Graduate
Dillon Consulting Limited
Calgary, AB · Edmonton, AB
- Full-time
…connected, including water mains, sanitary sewers, stormwater systems, and…
Added 5 mins ago
DC
Intermediate Civil Engineer/Civil Project Manager
Dillon Consulting Limited
Calgary, AB · Edmonton, AB
- Full-time
…connected, including water mains, sanitary sewers, stormwater systems, and…
Added 5 mins ago
DC
Senior Civil Engineer/Civil Project Manager
Dillon Consulting Limited
Calgary, AB · Edmonton, AB
- Full-time
…connected, including water mains, sanitary sewers, stormwater systems, and…
Added 5 mins ago
VC
Registered Nurse (RN) - Med/Surg - Acute Care Surgery
Vancouver Coastal Health
Vancouver, BC
- $41.42 to $55.91 CAD / hour
- Temporary
Added 5 mins ago
LH
Senior Program Manager
LGI Healthcare Solutions Santé Inc.
Montreal, QC
- Full-time
Bachelor’s degree in business administration, information systems, computer science, engineering, project management, or a related field.
Added 5 mins ago
AR
Assistant Front Office Manager
Algonquin Resort
St. Andrews, NB
- Full-time

AbCellera

Senior QC Data Reviewer

Vancouver, BC, Canada

$88,000 to $110,000 CAD / year

Apply About employer

Applications open in a new tab.

Job details

Pay: $88,000 to $110,000 CAD / year
Posting language: English
Posted: Oct 7, 2026

Original 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 that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown.

We're looking for an experienced QC Data Reviewer to support internal and external GMP testing across our clinical development programs. In this role, you'll provide independent review of analytical and microbiological data generated for release, stability, raw material, validation, qualification, and method transfer activities. You'll make sure every result is accurate, traceable, and compliant with approved methods, specifications, protocols, SOPs, and GMP requirements, with data integrity at the centre of your work. With a significant volume of QC activity ahead across multiple projects, your reviews will keep data moving and support timely product disposition. If you're a detail-driven QC professional who wants your work to directly help get clinical programs to the patients who need them, we'd love to hear from you.

How you might spend your days

Performing independent GMP review of analytical and microbiological data from internal QC laboratories and external testing partners, covering release, stability, raw material, in-process, drug substance, drug product, and placebo testing across techniques such as HPLC/UPLC, GC, UV/Vis, spectroscopy, wet chemistry, bioburden, endotoxin, environmental monitoring, and utilities testing
Reviewing raw data, calculations, chromatograms, spectra, instrument outputs, worksheets, and laboratory records for accuracy, completeness, traceability, and compliance with approved methods, specifications, protocols, SOPs, and GMP requirements
Verifying calculations, sample identification, acceptance criteria, and reported results, and escalating OOS, OOT, atypical results, trends, deviations, and other data irregularities
Ensuring laboratory data and records meet ALCOA+ data integrity expectations, including review of electronic records and audit trails
Reviewing data and reports for method development, qualification, validation, verification, and transfer activities, along with instrument and equipment qualification, calibration, and preventive maintenance records, and supporting completion of final study packages
Partnering with analysts and scientists to resolve documentation gaps, corrections, and incomplete testing in a timely and compliant manner
Providing technical review and scientific judgment in support of deviations, investigations, OOS/OOT assessments, root cause analysis, and CAPAs
Reviewing Certificates of Analysis, stability reports, and other controlled QC reports to support timely data release in line with program and manufacturing timelines
Supporting the preparation of analytical and microbiological content for regulatory submissions, providing QC support to program and CMC sub-teams, and contributing to the development and revision of QC SOPs, forms, templates, and work instructions
Driving continuous improvement in QC processes, data integrity, and reviewer practices by identifying recurring issues, coaching analysts and scientists on good documentation practices, and contributing to inspection and audit readiness

We’d love to hear from you if

You have a Master's degree in Chemistry, Biochemistry, Microbiology, Pharmaceutical Sciences, Life Sciences, or a related scientific field, with 5+ years of relevant GMP experience in pharmaceutical or biotechnology QC (a Bachelor's degree with significant additional relevant experience will also be considered)
You have hands-on experience in a GMP laboratory, including independent QC data review, with a strong ability to review analytical data from techniques such as UPLC, UV/Vis, ELISA, CE-SDS, iCIEF, spectroscopy, and wet chemistry (microbiology data review is an asset)
You have experience reviewing release, stability, method validation/qualification/verification, and method transfer data
You have strong knowledge of GMP, ALCOA+ data integrity principles, OOS/OOT, deviations, investigations, CAPA, and change control
You are comfortable working with laboratory systems such as Empower and LIMS
You critically evaluate analytical data to identify discrepancies, trends, documentation gaps, and issues that need escalation
You are detail-oriented and organized, managing multiple priorities against release, stability, manufacturing, and regulatory timelines
You communicate clearly, collaborate well across functions, and bring sound scientific judgment, accountability, and professionalism
You are proactive and solutions-focused, and comfortable making independent decisions in a fast-paced GMP environment
You have previous QA or independent GMP data-review experience (highly valued)

What we offer

AbCellera’s hiring range for this role is CAD $88,000 - $110,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, 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 is 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 23409 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.

Apply About employer

More about this job

Responsibilities

The Senior QC Data Reviewer will perform independent GMP reviews of analytical and microbiological data to ensure accuracy, traceability, and compliance with regulatory standards. They will partner with scientists to resolve documentation gaps and support the timely release of clinical products.

Requirements

Candidates must hold a Master's degree in a scientific field with at least 5 years of relevant GMP experience in pharmaceutical or biotechnology QC. Strong knowledge of ALCOA+ data integrity principles and hands-on experience with laboratory systems like Empower and LIMS are required.

Skills

GMP
Data integrity
Analytical data review
HPLC
UPLC
Microbiology
ALCOA+
OOS/OOT investigations
CAPA
Empower
LIMS
Method validation
Stability testing
Regulatory compliance
Technical writing
Quality control

Benefits

Equity
Annual bonus
RRSP contribution
Active lifestyle allowance
Annual vacation
Professional development
Health benefits
Scientific and technical mentorship

Visa sponsorship

Not detected in the job text

Keywords

GMP
Quality Control
Data Integrity
Pharmaceutical
Biotechnology
HPLC
UPLC
Microbiology
ALCOA+
OOS
OOT
CAPA
Empower
LIMS
Method Validation
Stability
Regulatory Submission
Documentation
Analytical Chemistry
Spectroscopy
Wet Chemistry
Bioburden
Endotoxin
Environmental Monitoring
Calibration
Preventive Maintenance
Root Cause Analysis
CMC
SOP
Clinical Development

Report this job