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Added 10 mins ago
RB
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Contract Duration: 6 months (with possibility for extension or conversion to FTE, depending on budget and performance)

Septodont

Production Supervisor II - Night

Cambridge, ON, Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Oct 27, 2026

Original job description

Location: Cambridge, Ontario - Onsite
Employment Type: Full-time
Schedule: Night Shift (Sunday to Thursday - 10 pm to 6 am)

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 a Production Supervisor II

JOB SUMMARY

The Production Supervisor II is accountable to the Production Manager for the operation of the shift through its material flow, human resources, documentation flow and training. This includes employees’ performance, efficient equipment operation, and in-process IPQC testing to meet the Company’s objectives and in accordance with the requirements outlined in the Standard Operating Procedures and Good Manufacturers Practices.

RESPONSIBILITIES

Coordinates shift changeover by ensuring: Machinery and human resources are optimal and report any deficiencies in a timely fashion. Availability of components and supplies. The area is clean and organized.
Maintains a visible presence on the production floor and resolves issues related to production/output.
Monitors job duties to ensure that all pertinent SOP’s are followed and all activities are documented properly. Issues, investigates and rectifies Quality Assurance deviations, including: Revising departmental SOPs and other GMP documents. Fixing documentation errors and coaching related operators on documentation practices.
Maintains a high degree of co-operation with other departments and participate in cross-departmental activities.
Acts as a resource to educate and train direct reports on the Safety Program. Holds employees accountable for following safety rules / regulations.
In conjunction with Production Managers and Human Resources Department, conduct Employee Relations activities such as: completion of employee performance reviews, carrying out performance improvement initiatives and guiding employee improvement action plans, recommend and administer disciplinary action, and guide conflict resolution by investigating employee complaints and initiating suitable resolution.
Coordinates new employee training and other training requirements of production staff through identifying training gaps and initiating cross training plans.
Drives GMP and regulatory requirements and ensures quality standards are met.
Completes Batch Record Reviews and daily shift reports for output, efficiency, downtime and other required matrix.
Models the Company Mission, Vision and Values Statements, policies, and current standard business practices.
Performs other related duties as required.

JOB REQUIREMENTS

Education

Degree in related a discipline such as Science or Engineering.
Formal Management or Professional Studies/Training or Certification would be an asset.

Experience and Skills

Minimum of 3 years of related experience in pharmaceutical manufacturing or a related environment with a combined minimum of 1 year of management experience.
Demonstrated people management and interpersonal skills with the ability to provide leadership.
Strong knowledge of Health and Safety legislation and other Employment related legislation such as Employment Standards Act.
Proven analytical and problem solving skills with the ability to make recommendations.
Demonstrated organizational skills with the ability to manage projects and multiple priorities with minimal direction.
Effective communication skills both verbal and written with the ability to delegate and to work within interdepartmental teams.
Excellent customer service and troubleshooting skills.
Must be able to attend all shifts.

Compensation

Starting at approximately $95,000.00 CAD with opportunity for increase based on qualifications and experience. Total rewards include comprehensive benefits, bonus eligibility, and professional development support.

What we Offer:

Excellent compensation/benefits package
RRSP Program
Discounted gym memberships
Programs supporting work life balance (EAP)
Corporate Discounts and PERKS
Employee recognition program
Social events and spirit days

Work Authorization: Applicants must be legally authorized to work in the country where the position is based for the duration of employment. This position is not eligible for employer-sponsored immigration support.

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.

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More about this job

Responsibilities

The Production Supervisor II manages shift operations, including material flow, human resources, and documentation to ensure efficient equipment operation. They are responsible for maintaining GMP compliance, conducting performance reviews, and overseeing training for production staff.

Requirements

Candidates must hold a degree in a related discipline such as Science or Engineering and possess at least 3 years of experience in pharmaceutical manufacturing. A minimum of 1 year of management experience is required, along with strong knowledge of safety legislation and GMP standards.

Skills

Pharmaceutical manufacturing
People management
GMP
SOP compliance
Quality assurance
Health and safety legislation
Analytical skills
Problem solving
Leadership
Batch record review
Training coordination
Interpersonal skills
Conflict resolution
Documentation management
Project management

Benefits

Comprehensive benefits
Bonus eligibility
Professional development support
RRSP program
Discounted gym memberships
Work life balance programs
EAP
Corporate discounts
Employee recognition program
Social events

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical manufacturing
GMP
SOP
Production supervision
Quality assurance
Batch record review
Health and safety
Employment standards act
Sterile injectable cartridges
CDMO
Industrial excellence
Performance management
Conflict resolution
Training
Documentation
Engineering
Science
Shift management
IPQC testing
Regulatory requirements

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