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Added 18 mins ago
JP
Senior Specialist, Microbiology & Environmental Monitoring
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
Job Title: Senior Specialist, Microbiology & Environmental Monitoring
Added 18 mins ago
JP
Specialist, Compliance
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
The Specialist, Compliance supports the Quality Systems & Compliance function by monitoring,maintaining, and strengthening site compliance with GMP and regulatory requirements.This role…
Added 18 mins ago
JP
Specialist, Compliance
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
We are seeking a detail-oriented and collaborative Specialist, Compliance to join our Quality team. In this role, you will support the maintenance and continuous improvement of our Quality…
Added 18 mins ago
JP
Senior Manager, Environmental Monitoring & Microbiology
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
The Specialist acts as a key quality partner to Operations by assessing EM risks, supporting investigations, trending data, and recommending scientifically sound corrective actions to…
Added 18 mins ago
JP
Maintenance Technical Specialist, Equipment and Documentation
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
Job Title: Maintenance Technical Specialist, Equipment and Documentation
Added 18 mins ago
JP
Spécialiste, Validation / Specialist, Validation
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
Job Title: Spécialiste, Validation / Specialist, Validation
Added 18 mins ago
JP
Validation Specialist
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
The Validation Specialist is responsible for developing, coordinating, and executing qualification and validation activities related to equipment, systems, utilities, cleaning processes,…
Added 18 mins ago
JP
Spécialiste, Validation AQ et gouvernance des données / Specialist, QA Validation & Data Governance
Jubilant Pharma Limited
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
…our team. In this key role, you will partner with Validation, Engineering, IT, Quality Control, and Operations teams to ensure systems, processes, and data remain compliant with regulatory…
Added 18 mins ago
K
Sea Logistics Customer Care Specialist
Kuehne+Nagel
Mississauga, ON
- Full-time
…keep goods moving efficiently. Whether you’re leading a team, engineering processes, or driving projects, your work ensures that our customers’ products are stored, handled, and delivered…
Added 18 mins ago
K
Sea Logistics Customer Care Specialist
Kuehne+Nagel
Winnipeg, MB
- Full-time
…keep goods moving efficiently. Whether you’re leading a team, engineering processes, or driving projects, your work ensures that our customers’ products are stored, handled, and delivered…
Added 2 hours ago
V
Specialist, Electrical Engineer
Vale
Sudbury, ON · Greater Sudbury, ON,CA
- Full-time
Provide engineering expertise for high-voltage electrical systems, substations, transmission and distribution infrastructure, generation equipment, and associated auxiliary systems.
Added 5 hours ago
AA
Ingénierie en Chef - Systèmes avion (train d'atterrissage, freins, air, carburant) / Chief Engineering - Aircraft Systems (Landing Gear, Brakes, Air, Fuel)
Airbus Aircraft
Montreal, QC
- Full-time
Added 6 hours ago
Y
GET
Yokogawa
NB · Chiasson Office, NB
- Full-time
…of industrial automation, test and measurement, information systems and industrial services in several…
Added 7 hours ago
AC
Engineer - Tooling
Air Canada
Toronto, ON
- Full-time
…Reporting to the Senior Manager, Technical Operations Tooling, the Engineering Specialist (Tooling) enjoys a broad scope of responsibility and works closely with the Senior Manager,…
Added 8 hours ago
HO
AI Governance Specialist
Hydro One
Toronto, ON
- $80 to $95 CAD / hour
- Contract
The AI Governance Specialist ensures that all AI models and related data assets comply with the organization's Enterprise AI Policy, Responsible AI principles, and regulatory obligations…
Added 9 hours ago
SM
RQ11880 – Systems Testing/QA Specialist – Senior
S M Software Solutions Inc
Toronto, ON
- Internship
Work Arrangement: Onsite – 5 Days per Week
Added 9 hours ago
SM
RQ11881 – Systems Testing/QA Specialist – Senior
S M Software Solutions Inc
Toronto, ON
- Internship
Work Arrangement: Onsite – 5 Days per Week
Added 9 hours ago
SM
RQ11688 – Systems Testing/QA Specialist – Senior
S M Software Solutions Inc
Toronto, ON
- Full-time
Work Arrangement: Onsite – 5 Days per Week
Added 10 hours ago
F
Lead Process Engineer- Mining & Metals
Fluor
Vancouver, BC
- Full-time
Minimum twelve (12) years of work-related experience, six (6) years of which must have been in an operating environment within the mining industry;
Added 11 hours ago
RT
Technical Account Manager (Water Treatment)
Rise Technical
Vancouver, BC
- $90,000 to $110,000 CAD / year
- Full-time
This is a permanent opportunity with a well-established specialist business, where you will inherit an existing book of business while taking ownership of the Vancouver metro area and…
Added 11 hours ago
GS
Ingénieur Fiabilité Lois de Commandes (Senior)
Groupe SII
Montreal, QC
- Full-time
You will work in the aerospace industry on safety-critical embedded systems, including flight control systems and controllers. You will contribute to assessing their safety and reliability…
Added 11 hours ago
GS
Programmeur FPGA (intermédiaire)
Groupe SII
Montreal, QC
- Full-time
As part of the development of critical computing systems for the aerospace industry, we are looking for an FPGA development, verification and validation specialist able to work within an…
Added 12 hours ago
H
Senior Identity and Reliability Engneering Specialist - Ping Forgerock
HRConnects
Montreal, QC
- Full-time
Senior Identity and Reliability Engineering Specialist – Ping / ForgeRock
Added 12 hours ago
SE
Heat Transfer Design Specialist
Siemens Energy
Montreal, QC
- Full-time
As a Heat Transfer Design Specialist in Additive Manufacturing at Siemens Energy you will immerse yourself in the development of sustainable design solutions for large gas turbines. Your…
Added 12 hours ago
AE
Specialist, Control Room
Agnico Eagle Mines Limited
Rankin Inlet, NU
- Full-time

Jubilant Pharma Limited

Validation Specialist

Greater Montreal Metropolitan Area, QC, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Dec 12, 2026
Posting language: English
Posted: Nov 12, 2026

Original job description

Job Description

Job Title: Validation Specialist

Req Id: 1572

Posting Start Date: 8/19/26

Job Description:

Role Overview

The Validation Specialist is responsible for developing, coordinating, and executing qualification and validation activities related to equipment, systems, utilities, cleaning processes, and manufacturing operations. This role partners closely with cross-functional teams to ensure compliance with regulatory requirements and current Good Manufacturing Practices (cGMP).

Key Responsibilities

Lead annual performance qualification activities for sterilization and depyrogenation equipment, including protocol development, execution, and reporting.
Develop and execute qualification protocols for equipment, systems, computerized systems, laboratory instruments, and utilities.
Prepare detailed validation protocols that include critical parameters, acceptance criteria, and sampling methodologies.
Assess the impact of equipment, raw material, or manufacturing process changes on validated systems and determine revalidation requirements.
Develop cleaning validation protocols in compliance with Health Canada, FDA, and EMA requirements.
Conduct risk assessments to justify cleaning limits and identify critical process parameters.
Participate in periodic qualification programs according to established procedures and timelines.
Review, write, and update standard operating procedures, work instructions, and forms.
Ensure protocols and reports comply with corporate standards and current Good Manufacturing Practices (cGMP).
Manage qualification projects in alignment with project plans, timelines, and the Validation Master Plan.
Provide validation support during the design, installation, commissioning, startup, and operation of new and existing equipment, systems, and utilities.
Participate in equipment evaluation, selection, and procurement activities.
Support new product introductions, quality investigations, CAPA activities, and change control assessments.
Execute decommissioning activities as required.
Perform additional duties as assigned.

Qualifications

Bachelor's degree in Engineering or Science.
Minimum three (3) years of experience in pharmaceutical manufacturing.
Hands-on experience writing qualification documentation and engineering studies.
Strong knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices.
Proficiency in Microsoft Office applications.
Proficiency with Kaye Validator software and instruments.
Bilingual in French and English, as the role supports operations outside of Quebec
Strong interpersonal and collaboration skills.
Quality-focused with exceptional attention to detail.
Strong analytical and problem-solving capabilities.
Membership in the Ordre des ingénieurs du Québec (OIQ) is considered an asset.
PMP certification is considered an asset.

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More about this job

Responsibilities

Develop, coordinate, and execute qualification and validation activities for equipment, systems, utilities, cleaning processes, and manufacturing operations, including sterilization and depyrogenation equipment. Manage validation projects and documentation while supporting equipment lifecycle activities, change control, new product introductions, investigations, and CAPA in compliance with regulatory requirements and cGMP.

Requirements

A bachelor's degree in Engineering or Science and at least three years of pharmaceutical manufacturing experience are required, along with hands-on experience writing qualification documentation and engineering studies. Candidates should know cGMP and Good Documentation Practices, be proficient with Microsoft Office and Kaye Validator software and instruments, and be bilingual in French and English; OIQ membership and PMP certification are assets.

Skills

Equipment Qualification
Process Validation
Cleaning Validation
Sterilization and Depyrogenation
Protocol Development
Risk Assessment
Good Manufacturing Practices
Good Documentation Practices
Change Control
CAPA
Quality Investigations
Kaye Validator
Microsoft Office
Analytical Problem-Solving
Cross-Functional Collaboration

Visa sponsorship

Not detected in the job text

Keywords

Validation
Qualification
Pharmaceutical Manufacturing
Current Good Manufacturing Practices
Good Documentation Practices
Sterilization
Depyrogenation
Cleaning Validation
Equipment Qualification
Computerized Systems
Laboratory Instruments
Utilities
Validation Protocols
Acceptance Criteria
Sampling Methodologies
Risk Assessment
Revalidation
Validation Master Plan
Standard Operating Procedures
Change Control
CAPA
Quality Investigations
New Product Introduction
Kaye Validator
Microsoft Office
Health Canada
FDA
EMA
OIQ
PMP

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Jobs in Canada