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Added 6 mins ago
Q
Lead Implementation Manager
Quandri
Vancouver, BC
- Full-time
You’ll work cross-functionally with Product, Engineering, CS, and Sales to ensure our customers have a seamless, high-impact implementation experience. You’re a builder. You thrive on…
Added 6 mins ago
J
High Voltage Equipment Specialist (HVDC/FACTS)
Jacobs
Ottawa, ON
- Full-time
…technical knowledge in the field of electrical high-voltage engineering, with emphasis on HVDC/FACTS, through past experience with consulting engineering firms, developers and/or direct…
Added 6 mins ago
J
High Voltage Equipment Specialist (HVDC/FACTS)
Jacobs
Toronto, ON
- Full-time
…technical knowledge in the field of electrical high-voltage engineering, with emphasis on HVDC/FACTS, through past experience with consulting engineering firms, developers and/or direct…
Added 6 mins ago
J
High Voltage Equipment Specialist (HVDC/FACTS)
Jacobs
Winnipeg, MB
- Full-time
…technical knowledge in the field of electrical high-voltage engineering, with emphasis on HVDC/FACTS, through past experience with consulting engineering firms, developers and/or direct…
Added 6 mins ago
J
High Voltage Equipment Specialist (HVDC/FACTS)
Jacobs
Calgary, AB
- Full-time
…technical knowledge in the field of electrical high-voltage engineering, with emphasis on HVDC/FACTS, through past experience with consulting engineering firms, developers and/or direct…
Added 6 mins ago
M
Specialist, Environmental Affairs
Morguard
Mississauga, ON
- Full-time
The Specialist, Environmental Affairs is accountable to the Manager, Environmental Affairs in the support, enhancement and promotion of Morguard’s environmental management system and…
Added 7 mins ago
B
AI Implementation Specialist, Calls
Buyerlink
Victoria, BC
- Full-time
We're looking for a curious, detail-oriented AI Implementation Specialist to join our team at an exciting inflection point. As AI becomes core to how we operate, you'll be the person…
Added 7 mins ago
E
Intermediate Fisheries Biologist
Engaged
ON · Ontario
- $70,000 to $85,000 CAD / year
- Full-time
Interpret field data, mapping, aerial imagery, GIS information, engineering drawings and design plans, and prepare clear, defensible biology reports, existing conditions assessments, impact…
Added 21 mins ago
RE
AI Solutions Specialist - Co-op Student (Winter 2027)
Rodan Energy Solutions Inc.
Mississauga, ON
- Internship
Integrate approved AI tools with systems, data sources, workflows, and documentation repositories where appropriate.
Added 36 mins ago
KG
IAM Automation Engineer (Python & PingDS Focus)
K&K Global Talent Solutions INC.
Quebec, QC
- Full-time
…integrations, and validation frameworks. If you are an identity specialist who loves writing code, optimizing Linux systems, and automating complex workflows via Python and Git, this role…
Added 37 mins ago
K
Liquids Control Centre (LCC) Supervisor
Keyera
AB · Liquid Infrastructure Regional Office
- Full-time
Discuss and align with Operations specialist on system operational improvements to maximize efficiency.
Added 37 mins ago
D
Programmer analyst, System and infrastructure operations, maintenance and development
Desjardins
Montreal, QC · Levis, QC
- Full-time
As a systems and infrastructure development, operations and maintenance programmer analyst, you participate in IT efficiency and quality by analyzing, designing, configuring, developing,…
Added 37 mins ago
BH
Account Manager - Downstream Chemicals
Baker Hughes
Leduc, AB
- Full-time
As a Sales Senior Specialist - Account Management, you will be responsible for:
Added 1 hour ago
C
IT Architecture Specialist-EN
CAE
Halifax, NS
- Full-time
Define integration patterns for systems and applications operating across hybrid environments, including on-premises and cloud platforms.
Added 1 hour ago
F
Responsable qualité senior / Senior Quality Specialist
FlatironDragados
Quebec, QC · Greater Quebec City Metropolitan Area
- Full-time
Are you passionate about ensuring excellence and compliance in every detail? As a Quality Specialist, you will play a crucial role in maintaining the highest standards by conducting…
Added 1 hour ago
C
Cyber Implementation Specialist-EN
CAE
Ottawa, ON
- Full-time
CAE Defence & Security Canada is seeking a Cyber Implementation Specialist to support the design, integration, implementation, and sustainment of cybersecurity solutions across Defence &…
Added 1 hour ago
C
IT Architecture Specialist-EN
CAE
Ottawa, ON
- Full-time
Define integration patterns for systems and applications operating across hybrid environments, including on-premises and cloud platforms.
Added 1 hour ago
C
IT Architecture Specialist-EN
CAE
Montreal, QC
- Full-time
Define integration patterns for systems and applications operating across hybrid environments, including on-premises and cloud platforms.
Added 1 hour ago
B
Branch Support Specialist
BMO
Toronto, ON · SCC
- Full-time
The Branch Support Specialist coordinates and supports Canadian branch technology operations, including break/fix, provisioning, deployments, activities, refresh programs, and branch…
Added 1 hour ago
SR
OT Controls Systems Specialist
Strathcona Resources Ltd.
Lloydminster, AB · Cold Lake, AB · Calgary, AB
- Full-time
We are seeking an experienced OT Control Systems Specialist to join the team responsible for the control systems, networks, infrastructure, and cyber security that Strathcona's field…
Added 1 hour ago
KI
International Trade Compliance Specialist
KBR, Inc.
Mississauga, ON
- Full-time
…Equipment Tracking, Regulatory and Customer Compliance of Property Systems, Import/Export Trade Compliance, Material Management, Stockrooms/Tool Cribs/Receiving, Engineering Tool Design and…
Added 1 hour ago
AW
Artificial Intelligence Specialist
Agilus Work Solutions
Toronto, ON
- Contract
…focused on connecting enterprise AI assistants to internal systems, building reusable AI capabilities, and helping business users turn real-world workflow challenges into scalable…
Added 1 hour ago
B
Branch Support Specialist
BMO
Toronto, ON
- Full-time
The Branch Support Specialist coordinates and supports Canadian branch technology operations, including break/fix, provisioning, deployments, activities, refresh programs, and branch…
Added 1 hour ago
P&
Spécialiste, Ingénierie Logicielle / Specialist, Software Engineering
Pratt & Whitney
Longueuil, QC
- Full-time
Added 1 hour ago
Bilingual Senior Specialist, Software Engineering (MW-AZURE)
CMHC - SCHL
Toronto, ON · Ottawa, ON · Montreal, QC
Join the Technology and Business Transformation team as part of the Software Engineering – Microsoft Azure group, in the Senior Specialist, Software Engineering position, where the next…

Septodont

Manufacturing Compliance Specialist

Cambridge, ON, Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Oct 30, 2026
Experience: A minimum of 3 years’ experience in the pharmaceutical industry, Quality Engineering or QA/QC
Posting language: English
Posted: Sep 30, 2026

Original job description

PRIMARY DUTIES AND RESPONSIBILITIES:

Conducts investigations for deviations following existing procedures.
Identifies and/or recognizes critical path for investigations leading to timely identification of root cause, corrective & preventative actions.
Ensure investigations are issued; tasks are appropriately assigned for completion or corrective and preventative actions and are closed in a timely fashion.
Works to facilitate, coordinate and investigate deviations with the relevant team and Subject Matter Experts (SME) to identify issues and root cause. Utilizes problem solving and root-cause analysis tools to facilitate the investigation.
Provides on-floor support, when possible, to assist the team with problem solving and help identify the root cause of issues.
Ensure investigations related to Operations are initiated and written as per existing procedure
Ensure identification of most probable root cause, corrective action & preventative action for all completed investigations. Writes and reviews investigation reports for completeness and accuracy prior to approval by Department Manager.
Conducts impact analysis of proposed corrective & preventative actions. Discuss findings with impacted departments (QA, RA, Validation, Production, etc.) and prepare recommendations for Department Managers.
Prepare and maintain lists, including status and next steps of open investigations for Cambridge Management.
Review on-going progress on relevant open investigations with Production Management to ensure alignment.
Facilitates the weekly deviation huddle and supports the team in achieving established key performance indicators (KPIs).
Project manages the corrective and preventative actions and assists in both implementation and follow-up.

BASIC REQUIREMENTS:

Education

University Degree in a related science.

Experience

A minimum of 3 years’ experience in the pharmaceutical industry, Quality Engineering or QA/QC
Fluency in project management &, Root Cause Analysis and Corrective Action Tools
Superb technical writing skills and abilities
Facilitating cross functional teams
Superior organizational, interpersonal communication skills
Ability to manage time effectively
Ability to work independently and manage multiple priorities in a fast-paced and changing environment
Good command of the English language, both written and verbal
Critical thinking skills with ability to problem solve
Knowledge of GMP
Proficiency with Word, Excel, and ERP systems

WORKING CONDITIONS:

The working conditions described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals to perform the essential functions.

Perform a variety of ordinary office tasks with light physical exertion such as intermittent walking, standing, sitting, etc.
Handling light-weight materials or documents
Regular visual concentration

Level of Work – Light

Light work is defined as exerting up to 9.0 kg of force on an occasional basis (0-33% of the workday), up to 4.5kg of force on a frequent basis (34.66% of the workday) and a negligible amount of force on a constant basis (67-100% of the work day).

Work Authorization: Applicants must be legally authorized to work in the country where the position is based for the duration of employment. This position is not eligible for employer-sponsored immigration support.

We are committed to diversity and inclusion, and thank all applicants in advance; however, we will be corresponding only with those selected for an interview.

In accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act, we are committed to providing an inclusive and barrier free recruitment and selection process.

Recruitment Fraud – please be aware of recruitment fraud. Novocol Pharmaceutical of Canada Inc. will never ask for banking information, money or any personal information up front. We will only respond to official applications submitted through our careers site. In addition, we will only use official corporate e-mail addresses (septodont.com or novocolpharma.com) to communicate with applicants. Should you be contacted without submitting an application, please delete the message and advise your e-mail provider.

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More about this job

Responsibilities

Investigate manufacturing deviations, identify root causes, and coordinate timely corrective and preventive actions with relevant teams and subject matter experts. Prepare and review investigation reports, track open investigations and action plans, and facilitate weekly deviation meetings to support performance targets.

Requirements

Requires a university degree in a related science and at least three years of experience in the pharmaceutical industry, Quality Engineering, or QA/QC. Candidates should have strong project management, root cause analysis, technical writing, communication, and organizational skills, along with GMP knowledge and proficiency in Word, Excel, and ERP systems.

Skills

Deviation Investigation
Root Cause Analysis
Corrective And Preventive Actions
Project Management
Technical Writing
Cross-Functional Team Facilitation
Problem Solving
Impact Analysis
GMP Knowledge
Investigation Report Writing
Organizational Skills
Interpersonal Communication
Time Management
Critical Thinking
Microsoft Word
Microsoft Excel

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical Industry
Quality Engineering
Quality Assurance
Quality Control
Good Manufacturing Practice
GMP
Deviation Investigation
Root Cause Analysis
Corrective And Preventive Actions
CAPA
Investigation Reports
Impact Analysis
Project Management
Problem-Solving Tools
Cross-Functional Teams
Subject Matter Experts
Key Performance Indicators
Production Management
Regulatory Affairs
Validation
Microsoft Word
Microsoft Excel
ERP Systems

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