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Added 14 mins ago
T
Director Enterprise Applications, Data
TEEMA
Vancouver, BC
- $160,000 to $215,000 CAD / year
- Full-time
Comes from a software engineering background. You’ve written production code and still think like an engineer, not just a manager of engineers.
Added 14 mins ago
T
Senior Product Manager – Digital Transformation | Agile & Product Roadmapping
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Toronto, ON
- Contract
We are seeking an experienced Senior Product Manager to lead digital product strategy, planning, and delivery within a complex IT environment.
Added 14 mins ago
NC
Parole Officer Supervisor
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AB · Edmonton, AB
- $70,000 to $100,000 CAD / year
- Full-time
Review community assessments and release plans and, having regular interactions and discussions with other staff working with the residents.
Added 28 mins ago
Sr. CAD Coordinator S5
OSI Maritime Systems
Burnaby, BC
Assigning work to CAD operators in coordination with the mechanical design manager;
Added 28 mins ago
Digital Product Manager, Member Experience
Canadian Federation of Independent Business
Canada
We are looking for a Digital Product Manager, Member Experience – Hybrid!
Added 28 mins ago
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Full Stack Developer
Alberta iGaming Corporation (AiGC)
AB · Edmonton, AB
- Full-time
…underpin Alberta's regulated iGaming market. Reporting to the Manager, Data Platforms, this position is responsible for end-to-end application development, from requirements gathering and…
Added 43 mins ago
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Lead Cloud Software Developer - (AWS / AI / Real Time Payment Systems)
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Toronto, ON · BMOPLACE
- Full-time
Follows release management processes and standards and applies version controls.
Added 43 mins ago
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Aircraft Structures Technician (C-17)
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Calgary, AB · Richmond, BC · Vancouver, BC · Winnipeg, MB · Trenton, NS · Mississauga, ON · Ottawa, ON · Toronto, ON · Montreal, QC · CAN - CFB Trenton, Canada
- Full-time
The Aircraft Structures Technician will work directly under the guidance of the Lead Structure Technician and report directly to the onsite Maintenance Manager.
Added 57 mins ago
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SOFTWARE ENGINEERING SPECIALIST - Technical Leader
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Montreal, QC
- Full-time
…teams in the domain, as well as with analysts, the product manager, and the solutions architect within their…
Added 1 hour ago
Associate Product Manager
PBS Systems
Calgary, AB
Dealer Image Pro is looking for an Associate Product Manager to help keep day-to-day product work moving. Working closely with the VP of Product, this person will help manage product…
Added 1 hour ago
Associate Product Manager
PBS Systems
Calgary, AB
Dealer Image Pro is looking for an Associate Product Manager to help keep day-to-day product work moving. Working closely with the VP of Product, this person will help manage product…
Added 1 hour ago
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Senior Product Manager
CQ Search Group Ltd.
Toronto, ON
- Contract
Our client, the Ministry of Public and Business Service Delivcery located in downtown Toronto has a 6 month contract for a Senior Product Manager.
Added 1 hour ago
Aircraft Technician Mechanic (ACA)
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Petawawa, ON
…Officer (SAMEO) (or designate) and CFO (Contractor Field Office) Manager (or…
Added 2 hours ago
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Senior DevOps Specialist (Azure Cloud)
Equisoft
Montreal, QC · Quebec, QC · HYBRID - Montreal, Canada
- Full-time
Role: The Senior DevOps Specialist (Azure Cloud) reports to the Manager, SaaS Operations and works closely with 3 other DevOps Specialists. The candidate helps design quality…
Added 2 hours ago
EC
AEM Engineer
Experis Canada
Toronto, ON
- Contract
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Added 2 hours ago
Application Specialist - Power & Drives
Spartan Controls Ltd.
Calgary, AB
…required bid documentation. Check accuracy and consistency before…
Added 3 hours ago
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Software Engineer Manager
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- $150,000 CAD / year
- Full-time
We seek a hands-on Engineering Manager to lead ContentIQ's development, quality, delivery, and operation. You'll mentor engineers while actively coding, making architectural decisions, and…
Added 3 hours ago
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Client Care Coordinator
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Vancouver, BC
- Full-time
Reporting to the Program Manager (PM) or designate, the Client Care Coordinator works collaboratively as part of an interdisciplinary team and within a trauma informed model of care and…
Added 4 hours ago
RL
Mechanical Engineer
RBR Ltd.
Ottawa, ON
- $100,000 to $150,000 CAD / year
- Full-time
Own mechanical designs from concept to production release, including analysis, modelling, prototyping, testing, iterating, and documentation
Added 6 hours ago
SP
Bilingual Customer Success Manager (French/English)
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Montreal, QC
- Full-time
The Customer Success Manager (CSM) is a versatile expert responsible for ensuring high-value customers who purchase the Signature Success Plan achieve a significant return on their…
Added 8 hours ago
DB
Consultant Pathologist - Sikar
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- Full-time
Release critical, high-value, high-risk reports with history-backed interpretation.
Added 10 hours ago
CO
Application & Integration Technical Analyst
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Saint John, NB
- Full-time
Under the direction of the designated IT Manager, the Application and Integration Technical Analyst is a technical lead responsible for system architecture, data strategy, and integration…
Added 11 hours ago
SJ
Admin Support 9 - Staffing Clerk
St. Joseph's Healthcare Hamilton
Hamilton, ON · Charlton Campus
- Part-time
This position supports the activities of the Clinical Manager of the Operational Command Center as they relate to the day-to-day staffing operations of units within the scope of the…
Added 12 hours ago
MANAGER DEVELOPMENT ENGINEERING
City of Toronto
Toronto, ON
Reporting to the Project Director in the Engineering Review Section, the Manager of Development Engineering provides the technical, financial, and administrative oversight needed to…
Added 12 hours ago
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Support Worker
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Monitors Sign In/Out and release conditions of CRF clients;

Replimune

Laboratory GxP Systems Specialist II

Montreal, QC, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Nov 25, 2026
Education: Bachelor’s degree
Experience: Minimum 5-8 years of experience administering computerized systems in a regulated GxP environment.
Posting language: English
Posted: Oct 26, 2026

Original job description

Overview

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.

At Replimune, We Live By Our Values

United: We Collaborate for a Common Goal.

Audacious: We Are Bold.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.

Join us, as we reshape the future.

Summary Of Job Description

The Laboratory GxP Systems Administrator is responsible for the administration, maintenance, compliance, and support of laboratory computerized systems used within a regulated GxP environment. The role serves as the primary liaison between laboratory users, Quality Assurance, IT, Validation, and system vendors to ensure laboratory systems remain secure, available, compliant, and maintained in a validated state.

This position is based in our Milton Park location and typically has a 5-day on-site expectation.

Key Responsibilities

Laboratory Computerized Systems Administration

Administer laboratory computerized systems, including user access management, system configuration, workflows, roles, permissions, reporting, and periodic access reviews.
Maintain system inventories, asset records, software version information, backups, archives, and associated lifecycle documentation.
Coordinate software installations, upgrades, patches, maintenance activities, and system monitoring, escalating issues and managing resolution with IT, vendors, and other stakeholders as required.
Support system reliability, cybersecurity, data integrity, disaster recovery, and troubleshooting of laboratory applications and instrument software.

Quality and Compliance Activities

Author, review, and support change controls, deviations, CAPAs, impact assessments, and other quality records associated with laboratory computerized systems.
Support validation inventories, compliance assessments, audit and inspection readiness activities, and serve as a subject matter expert during internal audits and regulatory inspections.

Vendor and Project Management

Coordinate activities performed by software vendors, consultants, and external validation contractors, including review of vendor documentation, release notes, service reports, and software lifecycle records.
Participate in cross-functional projects involving laboratory systems and digital solutions, tracking deliverables, timelines, risks, and actions through implementation, testing, validation, and qualification activities, including FAT, SAT, commissioning, and qualification where applicable.

Training and Continuous Improvement

Develop and deliver user training, provide guidance on compliance and data integrity requirements, and support the development and revision of SOPs, work instructions, and lifecycle management procedures.
Drive continuous improvement initiatives related to laboratory computerized systems, system administration practices, and computer system validation processes.

Other Responsibilities

Ensure all activities are performed in accordance with SOPs, cGMP requirements, GDocP requirements, quality standards, and safety procedures.
Maintain personal training compliance and qualification requirements for assigned responsibilities.
Support laboratory and quality-related investigations involving computerized systems.
Participate in after-hours support activities when required for business continuity.

Educational Requirements

Bachelor's degree in Life Sciences, Chemistry, Biotechnology, Engineering, Computer Science, Information Systems, or related discipline required.
Advanced degree or relevant professional certifications desirable.

Experience And Skill Requirements

Minimum 5-8 years of experience administering computerized systems in a regulated GxP environment.
Working knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, ALCOA+, Windows/Active Directory environments, laboratory systems, software lifecycle, periodic review, and supplier assessment.
Experience with change control, deviations, CAPAs, and quality management systems.
Strong technical writing, communication, organization, stakeholder management, problem-solving, attention to detail, and ability to work independently and in cross-functional teams.

Preferred Competencies

Experience with viewLinc, Empower, SoftMax Pro GxP, PharmSpec, BlueMountain Regulatory Asset Manager, LIMS, QuantStudio Design and Analysis software, and / or JMP software.
Experience with Computer System Validation (CSV) and Data Integrity principles.
Knowledge of pharmaceutical, biotechnology, or cell and gene therapy laboratory operations.
Experience supporting cloud-hosted and SaaS-based GxP applications.
Experience assessing and implementing software updates and cybersecurity patches within a validated environment.

About Replimune

Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.

We are an Equal Opportunity Employer.

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More about this job

Responsibilities

Administer and maintain laboratory computerized systems in a regulated GxP environment, including access, configuration, lifecycle records, upgrades, troubleshooting, security, and data integrity. Coordinate quality and validation activities, vendor and project work, audits, training, and continuous improvement to keep systems compliant and in a validated state.

Requirements

A bachelor's degree in a relevant scientific, engineering, or information technology discipline is required, along with 5–8 years of experience administering computerized systems in a regulated GxP environment. Candidates should have working knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, ALCOA+, laboratory systems, and quality processes; experience with CSV and data integrity is preferred.

Skills

GxP Systems Administration
Computer System Validation
Data Integrity
Change Control
Deviation and CAPA Management
Quality Management Systems
GAMP 5
21 CFR Part 11
EU Annex 11
Windows and Active Directory
Laboratory Systems
Supplier Assessment
System Lifecycle Management
Cybersecurity
Technical Writing
Stakeholder Management

Visa sponsorship

Not detected in the job text

Keywords

GxP
GAMP 5
21 CFR Part 11
EU Annex 11
ALCOA+
Computer System Validation
Data Integrity
Windows
Active Directory
ViewLinc
Empower
SoftMax Pro GxP
PharmSpec
BlueMountain Regulatory Asset Manager
LIMS
QuantStudio Design and Analysis
JMP
Change Control
Deviations
CAPA
Quality Management Systems
Supplier Assessment
Periodic Review
SaaS
Cybersecurity Patches
FAT
SAT
Commissioning
Qualification
cGMP

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