Compounder

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…