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Septodont

Compounder

Cambridge, ON, Canada

Job type: Full-time
Apply by: Oct 25, 2026
Experience: A minimum of 1 year related work experience in a manufacturing environment
Posting language: English
Posted: Sep 25, 2026

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Applications open in a new tab.

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?

We have an opportunity for you!

This position is starting at $28/hour.

FUNCTION SUMMARY:

The Compounder is accountable to the Production Supervisor for all activities relating to the compounding and transfer filtration of dental products to meet the company’s objectives and in accordance with the requirements outlined in Standard Operating Procedures and Good Manufacturers Practices.

PRIMARY DUTIES AND RESPONSIBILITIES:

Completes batch bulk product, silicone solutions, disinfectants and other manufacturing solutions and record manufacturing formula and procedure according to the Batch Record
Performs and documents results of quality tests and required cleaning protocols in appropriate log books and the Batch Record
Informs supervisor of any production problems
Conducts set-up, filter and monitor media solution as required
Performs product changeovers
Performs and records all line clearance, cleaning and sanitization tasks as completed
Participates in special projects, equipment and process validation.
Monitors and recommends procedural changes as identified
Investigates batch information and related issues to summarize and report findings
Operates and cleans Terminal Sterilizers (TS)
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. A college certification/diploma or equivalent is an asset.

Experience

A minimum of 1 year related work experience in a manufacturing environment
Pharmaceutical, food, or cosmetic industry experience is considered an asset
Demonstrated ability to work any shift in a 24/7 environment
Strong attention to detail
Ability to work in fast paced environment
Team oriented

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

Compound and transfer-filter dental products and manufacturing solutions, documenting formulas, procedures, quality tests, and cleaning activities in batch records and logbooks. Operate and clean terminal sterilizers, support changeovers and validations, investigate batch issues, and follow GMP, regulatory, quality, and safety requirements.

Requirements

A high school diploma is required; a college certificate or diploma is an asset. Applicants need at least one year of related manufacturing experience, the ability to work any shift in a 24/7 environment, strong attention to detail, and the ability to work in a fast-paced, team-oriented setting.

Skills

Compounding
Transfer Filtration
Batch Record Documentation
Quality Testing
Cleaning and Sanitization
Media Solution Filtration
Product Changeovers
Line Clearance
Process Validation
Equipment Validation
Batch Investigation
Terminal Sterilizer Operation
Good Manufacturing Practices
Regulatory Compliance
Attention to Detail
Teamwork

Visa sponsorship

Not detected in the job text

Keywords

Dental Products
Pharmaceutical Manufacturing
Contract Manufacturing
Compounding
Transfer Filtration
Batch Records
Manufacturing Formulas
Quality Testing
Cleaning Protocols
Media Solutions
Product Changeovers
Line Clearance
Sanitization
Process Validation
Equipment Validation
Batch Investigation
Terminal Sterilizers
Good Manufacturing Practices
GMP
Regulatory Requirements
Quality Standards
Safety Guidelines
Manufacturing Environment
Pharmaceutical Industry
Food Industry
Cosmetic Industry
24/7 Shift Work

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