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Added 9 mins ago
F-
Intermediate Architectural Technologist
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- Full-time
Excel at Revit (modeling, detailing and family creation) for the production of technical drawings, AutoCAD an asset.
Added 9 mins ago
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- $70 to $80 CAD / hour
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Added 9 mins ago
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Spécialiste Qualité - Electronics Quality Control Specialist
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- $30 to $45 CAD / hour
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Added 9 mins ago
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Spécialiste Qualité - Electronics Quality Control Specialist
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- $30 to $45 CAD / hour
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Added 9 mins ago
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Spécialiste Qualité - Electronics Quality Control Specialist
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Montreal, QC
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Added 9 mins ago
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- $30 to $45 CAD / hour
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Added 9 mins ago
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Spécialiste Qualité - Electronics Quality Control Specialist
Actalent
Montreal, QC
- $30 to $45 CAD / hour
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Added 9 mins ago
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Added 9 mins ago
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Added 9 mins ago
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Added 9 mins ago
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Test Technologist
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- $25 to $35 CAD / hour
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Added 25 mins ago
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Montreal, QC
- Full-time
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Added 25 mins ago
M
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Added 25 mins ago
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Added 39 mins ago
HM
Grower
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- $79,374.38 to $92,603.44 CAD / year
- Full-time
…will always be in clear and frequent contact with the Material Application…
Added 40 mins ago
WG
Production Labour - Manufacturing
WGI Group
Corman Park No. 344, SK
- Full-time
We are looking for a Material Handler to support our plastic drainage pipe manufacturing operations. In this active role, you will help operate production lines, handle and package…
Added 54 mins ago
TT
CNC Machining Centre Programmer
Titan Trailers Industries Limited - UK
Tillsonburg, ON
- Full-time
This position works closely with Senior Management, Finance, Production, Supply Chain, and Operations to support data-driven decision-maki

Septodont

Set-up Operator I

Cambridge, ON, Canada

Full-time

Apply About employer

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Job details

Job type: Full-time
Experience: A minimum of one year of related work experience in a manufacturing environment, however 2 years or more of work experience is considered an asset
Posting language: English
Posted: Sep 15, 2026

Original job description

At Septodont, a global leader in dental products and a key player in pharmaceutical development and contract manufacturing (CDMO), we are proud to work every day to improve patients’ health and well-being.

Present in more than 110 countries, the Group relies on the energy, expertise, and passion of 2,600 employees. With 6 international production sites, Septodont combines industrial excellence, technological expertise, and innovation to meet the needs of healthcare professionals worldwide.

In North America, our operations include facilities in Ontario, Quebec, and Pennsylvania. Our Cambridge, Ontario site is home to Novocol Pharma – a thriving center of innovation with over 40 years of expertise in sterile injectable cartridges and combination product manufacturing. Backed by a team of more than 675 dedicated professionals and modern facilities, we deliver high-quality, customer-focused solutions to partners around the world.

Beyond our expertise, our people are our greatest strength. We foster a stimulating work environment where everyone can learn, grow, and build a career that reflects their aspirations, supported by continuous training and internal mobility. As a socially responsible company, we place diversity and inclusion at the heart of our development, convinced that they enhance collective performance and foster human experience.

Joining Septodont means becoming part of a human-scale international group and contributing to a meaningful mission: improving health for as many people as possible. What if your next professional chapter started with us?

Shift Available:

Night Shift - Sunday to Thursday - 10pm to 6am - Shift Premium $3/hour

This position is starting at $27/hour, plus shift premium.

FUNCTION SUMMARY:

The Set-up Operator I is accountable to the Production Supervisor for all activities relating to the set-up of all inspection, labeling and packaging (ILP) equipment, trouble-shooting, mechanical adjustments, and preventative maintenance, in order to meet the company’s objectives. These activities will be performed in accordance with the requirements outlined in Company Policies, Standard Operating Procedures and Good Manufacturing Practices.

PRIMARY DUTIES AND RESPONSIBILITIES:

Sets up and disassembles all inspection, labeling and packaging machines
Trains new ILP operators on inspection machine, labeling machine and packaging line operation
Performs basic trouble shooting, mechanical adjustments, interventions and preventative maintenance on the ILP machines
Reports any equipment problems and process related downtime to the area Lead Hand, Maintenance Technician, and Supervisor and work together to solve them
Ensures that the ILP areas run smoothly by informing the area Lead Hand and/or Supervisor when supplies are needed
Makes suggestions for improving training programs and ILP area processes and participate in continuous improvement initiatives
In the absence of the Lead Hand, performs back-up duties and responsibilities as assigned
Monitors and reviews system entries, ensure that scanned data is accurate
Creates maintenance work orders and requests using the CARL system
Reviews batch record entries and assist with audit corrections
Ensures all GMPs, SOPs, and company policies are followed
Assists with Q-Note and DIR Investigations as required
Takes on the role of the Operator as needed
Follows GMP and regulatory requirements, and ensures quality standards are met
Observes and supports all safety guidelines and regulations
Demonstrates the Company Mission, Vision and Values Statements, policies, and current standard business practices
Performs other related duties as required

BASIC REQUIREMENTS:

Education

High school diploma

Experience

A minimum of one year of related work experience in a manufacturing environment, however 2 years or more of work experience is considered an asset
Pharmaceutical, food, or cosmetic industry experience is considered an asset
Demonstrated mechanical experience or mechanical aptitude
The ability to work any shift in a 24/7 environment

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.

Apply About employer

More about this job

Responsibilities

The Set-up Operator I is responsible for the setup, troubleshooting, and preventative maintenance of inspection, labeling, and packaging equipment. They also train new operators and ensure all activities comply with Good Manufacturing Practices and company policies.

Requirements

Candidates must have a high school diploma and at least one year of manufacturing experience, with preference given to those with pharmaceutical or mechanical backgrounds. Applicants must be legally authorized to work in Canada and capable of working in a 24/7 environment.

Skills

Equipment setup
Mechanical troubleshooting
Preventative maintenance
Machine operation
GMP compliance
SOP adherence
Data entry
Quality control
Training
Mechanical aptitude
Packaging line operation
Labeling machine operation
Inspection machine operation
Audit support
Safety compliance

Benefits

Shift premium

Visa sponsorship

Not detected in the job text

Keywords

Manufacturing
Pharmaceutical
Sterile injectable cartridges
CDMO
Good Manufacturing Practices
GMP
Standard Operating Procedures
SOP
Mechanical aptitude
Preventative maintenance
Troubleshooting
Packaging
Labeling
Inspection
CARL system
Batch records
Quality standards
Safety guidelines
Continuous improvement
Industrial excellence

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