S

Septodont

Verified Job Source

We enhance lives by providing innovative, safe and effective healthcare solutions

Saint-Maur-des-Fossés

Medical Equipment Manufacturing
1,001–5,000 people

About

Septodont is a pharmaceutical and medical device company and was founded in 1932 by Annie & Nestor Schiller. With 600 million cartridges of local anesthetic produced every year, Septodont is today world leader of dental anesthesia. Beyond dental anesthesia, Septodont also invests in R&D towards bioactive and biocompatible therapeutic solutions, which led to the introduction of Biodentine and Bioroot RCS, two products based on the ABS Technology (Active Biosilicate Technology). The group counts 2,600 employees and remains a 100% family owned company under the leadership of its CEO, Karim Khadr.

Open positions

Maintenance Technician

On-site

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,…

Metrology Specialist

On-site

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,…

Material Handler

On-site · Cambridge

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 Cambri…

Set Up Operator I

On-site · Cambridge

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 Cambri…

Filling Specialist

On-site · Cambridge

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 Cambridg…

Maintenance Manager

On-site · Cambridge

The Maintenance Manager leads a multidisciplinary team to plan and execute preventive and corrective maintenance for GMP manufacturing equipment. They are responsible for optimizing equipment performance, managing departmental budgets, and ensuring compliance with safety and regulatory standards.

Production Project Lead

On-site · Cambridge

The Production Project Lead acts as the primary production representative on cross-functional projects, ensuring successful integration of commercial production activities. They are responsible for managing project schedules, facilitating technology transfers, and ensuring all manufacturing activities comply with GMP and SOP standards.

Product Development Engineer

Hybrid · Bromont

The Product Development Engineer will design and develop innovative medical devices, managing projects from initial concept through prototyping, testing, and production transfer. This role involves performing iterative CAD design, executing performance validation, and maintaining technical documentation in compliance with regulatory standards.

Process Specialist II /Engineer II

On-site · Cambridge

The Process Engineer/Specialist is responsible for leading engineering projects, managing process system support, and driving continuous improvement initiatives within a regulated manufacturing environment. They will also oversee equipment qualification, validation activities, and ensure compliance with quality and regulatory standards.

Lead Hand III

On-site · Cambridge

The Lead Hand III is responsible for overseeing compounding and filling manufacturing activities, including resource allocation, equipment operation, and team training. They ensure compliance with Good Manufacturing Practices and Standard Operating Procedures while driving continuous improvement and quality standards.

Manufacturing Compliance Specialist

On-site · Cambridge

The Manufacturing Compliance Specialist conducts investigations into deviations, identifies root causes, and implements corrective and preventative actions. They also facilitate cross-functional collaboration and ensure all investigation reports meet regulatory and internal standards.

Microbiologist I

On-site · Cambridge

The Microbiologist I performs essential laboratory testing including environmental monitoring, sterility, bioburden, and pyrogen testing in an aseptic processing environment. They also support quality investigations, maintain gowning certifications, and ensure compliance with GMP and safety regulations.

Production Operator

On-site · Cambridge

Operators are responsible for the preparation, filling, and packaging of sterile injectable products while adhering to strict GMP and safety standards. They must maintain cleanroom environments, complete batch documentation, and perform quality inspections to ensure product integrity.

Set Up Operator I

On-site · Cambridge

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 GMP and company safety standards.

Compounder

On-site · Cambridge

The Compounder is responsible for the compounding and transfer filtration of dental products in accordance with Standard Operating Procedures and Good Manufacturing Practices. They must perform quality tests, maintain accurate batch records, and ensure all cleaning and sanitization protocols are followed.

Set-up Operator I

On-site · Cambridge

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.

Project Manager II

On-site · Cambridge

The Project Manager II leads cross-functional teams to deliver complex projects on time and within budget, ranging from new business development to technology transfer. They are responsible for project governance, risk management, and serving as the primary point of contact for CDMO clients.

Maintenance Millwright (443A)

On-site · Cambridge

Responsible for the repair, modification, and preventive maintenance of production and supporting equipment to ensure operational continuity. Performs root-cause analysis of breakdowns and supports continuous improvement projects within a GMP environment.