General information
Position description
Category
Operations - Manufacturing
Job Title
Compounder
Company Details
Septodont is a leading manufacturer of dental pharmaceuticals and medical devices. The French-based company employs over 2,000+ people globally. We have six manufacturing plants in France, India, North and South America, and an international distribution network that is dedicated to serving the needs of dental professionals in more than 150 countries. Our North American operations have facilities in Ontario, Montreal, and Pennsylvania. It also has Latin American operations with facilities in Brazil and Colombia.
Our Cambridge, Ontario site is also home to our Novocol Pharma division, which focuses on contract development and manufacturing, specialized in sterile injectable cartridge and combination product manufacturing.
Our employees are our number one asset! We offer developmental opportunities, excellent compensation and benefit programs, discounted gym memberships, work/life balance programs, employee recognition, social events and spirit days.
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.
Internal Applications:
Job level: 6B
Currently hiring for one (1) Compounder on Afternoon shift.
If you are interested in the Compounder position on any shift, please upload your resume to the Internal Job Application Site no later than February 17, 2025, and include your shift preference in the application. We will be referring to this posting for future Compounder openings in the next 3 months.
NOTE: For employees that do not currently have access to the internal job application site, please email your application, to Lesley Cooper, Senior TA Specialist, lcooper@septodont.com.
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.
Contract type
Permanent
Position location
Job location
North America, Canada, Cambridge
