Skip to main content
All Jobs Listings
  • Full Time
  • Cambridge
  • November 14, 2022
  • Hours: 40

Website Septodont

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.

We are currently recruiting for the Weekend Day Shift (Thursday and Friday 6AM-2PM and Saturday and Sunday 6AM-6PM)

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.

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

Candidate criteria
Minimum level of education required
1 – High School

Minimum level of experience required
Less than 2 years

How to apply:

Via Agilec - jfruhner-travers@agilec.ca

Q

    Send us a note

    Please use the contact form below or feel free to contact Agilec at 1-800-361-4642.

    Pin It on Pinterest

    Share This