Compounder at Septodont

Company detail

Grow with us! Septodont is a global leader in dental pharmaceuticals and medical devices, employing over 2,000 people worldwide and operating six manufacturing plants across France, India, North and South America. With an international distribution network serving dental professionals in more than 150 countries, Septodont is committed to improving patient care globally.




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 693 dedicated professionals and modern facilities, we deliver high-quality, customer-focused solutions to partners around the world.




Join us and be part of a company that values integrity, collaboration, and the drive to make a real difference. Together, we are shaping the future of patient care and improving lives every day.

We have an opportunity for a Compounder.

Job 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.

Available Shifts:

Nights: Sunday - Thursday 10:00PM - 6:00AM.

Weekend Night Shift: Saturday and Sunday 6:00PM - 6:00AM, Friday 10:00PM-6:00AM, Monday 10:00PM - 6:00AM.

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.

Qualifications

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.