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Septodont

Quality Systems & Continuous Improvement Specialist

Cambridge, ON, Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Oct 19, 2026

Original job description

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 Quality Systems & Continuous Improvement Specialist in Cambridge, ON.

FUNCTION SUMMARY

The Quality Systems & Continuous Improvement Specialist is accountable to the Senior Manager, Quality and is responsible for providing quality and compliance leadership within a cross-functional continuous improvement team. The Quality Systems & Continuous Improvement Specialist will partner with Production, Engineering, Technical Services, Validation, and Quality personnel to identify, prioritize, and implement improvements that enhance manufacturing performance, product quality, and quality system effectiveness.

The Quality Systems & Continuous Improvement Specialist will provide quality oversight and regulatory guidance for continuous improvement initiatives and quality event management activities. This role will lead and support investigations, risk assessments, and corrective and preventive actions (CAPAs) to ensure issues are effectively resolved and improvements are implemented in a compliant and sustainable manner.

Success in this position requires a strong presence on the manufacturing floor, actively observing processes, engaging with operators and technical staff, identifying emerging issues and opportunities, and applying critical, innovative thinking to drive practical and effective solutions. The incumbent will leverage GMP and regulatory requirements using a risk-based approach, balancing quality, compliance, operational performance, and business objectives. In addition, this role will be instrumental in accelerating the maturation of newly implemented procedures and quality system processes, ensuring they are robust, effective, and sustainable components of the organization’s Quality Management System.

PRIMARY DUTIES AND RESPONSIBILITIES:

Partner with Production, Engineering, Technical Services, Validation, and Quality teams to identify and implement improvements to manufacturing processes, equipment, systems, and procedures that enhance product quality, process capability, and operational performance
Maintain a strong presence within manufacturing operations to develop a thorough understanding of processes, identify improvement opportunities, and support sustainable operational and quality excellence.
Provide quality and regulatory guidance to cross-functional teams and continuous improvement initiatives, ensuring compliance with GMP regulations, industry standards, and regulatory expectations.
Review and assess proposed process, equipment, facility, and procedural changes for quality and regulatory impact.
Apply critical thinking, scientific analysis, risk-based decision making, and structured problem-solving methodologies to investigate issues, identify root causes, challenge conventional approaches, and develop effective solutions.
Lead and/or facilitate investigations related to deviations, complaints, audit observations, environmental monitoring excursions, and other quality events, ensuring investigations are thorough, scientifically sound, and completed within established timelines.
Lead and/or support the development, implementation, effectiveness verification, and on-time closure of corrective and preventive actions (CAPAs) and other quality event actions.
Lead and/or facilitate quality risk assessments and ensure quality risks are appropriately identified, evaluated, and mitigated.
Monitor and trend manufacturing and quality system performance data to identify recurring issues, emerging risks, and opportunities for improvement.
Lead and support the design, implementation, and maturation of quality systems, procedures, and business processes, ensuring they are effective, compliant, sustainable, and aligned with organizational objectives.
Partner with operational teams to establish process controls, performance metrics, and feedback mechanisms that drive process capability, consistency, continuous improvement, and operational effectiveness.
Identify opportunities to simplify processes, improve product quality, process capability, and operational performance, and reduce compliance risk while maintaining patient safety and regulatory compliance.
Participate in internal and external audits, regulatory inspections, and inspection readiness activities as required.
Develop and report quality metrics related to investigations, CAPAs, quality events, quality systems, and continuous improvement initiatives.
Facilitate cross-functional meetings and ensure action items are appropriately assigned, tracked, and completed on time.
Provide training, coaching, and guidance related to investigation practices, root cause analysis, risk management, continuous improvement, and quality system requirements.
Demonstrates the company's core values, policies, and standard business practices.
Performs other related duties as required.

BASIC REQUIREMENTS

EDUCATION

A minimum of a Bachelor's degree in Engineering, Life Science, Physical Science or a related field, from a recognized academic institution.

An individual possessing a Professional Engineer (P.Eng.) license is an asset.

EXPERIENCE

Minimum five years' experience in a pharmaceutical, biologics, medical device, or other GMP-regulated manufacturing environment.

Experience leading investigations, CAPAs, and continuous improvement initiatives.

Demonstrated ability to rapidly learn and develop expertise in manufacturing processes, deeply understand how systems operate, identify opportunities for transformational improvement, and develop innovative solutions that challenge traditional thinking while improving product quality, process capability, and operational performance.

Strong knowledge of GMP regulations, quality systems, and risk management principles.

Experience working within manufacturing, engineering, technical services, validation, or quality functions.

Working knowledge of Health Canada, FDA, EU GMP, and applicable industry standards.

Strong facilitation, communication, project management, and problem-solving skills

KNOWLEDGE AND SKILLS

Strong understanding of pharmaceutical manufacturing processes and quality systems.
Ability to interpret and apply regulatory requirements using a practical, risk-based approach.
Ability to balance compliance requirements with operational and business objectives.
Strong analytical and critical-thinking skills.
Effective collaboration and influencing skills within cross-functional teams.
Proficiency in root cause analysis, risk assessment, and continuous improvement methodologies.

Compensation

Starting at approximately $94,000.00 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

Partner with manufacturing and quality teams to improve processes, equipment, procedures, and quality systems while providing risk-based GMP and regulatory guidance. Lead or facilitate investigations, risk assessments, CAPAs, performance monitoring, audits, and training to ensure compliant, sustainable improvements.

Requirements

Requires a bachelor's degree in engineering, life science, physical science, or a related field, and at least five years of experience in a GMP-regulated manufacturing environment. Candidates should have experience with investigations, CAPAs, continuous improvement, quality systems, risk management, and applicable Health Canada, FDA, and EU GMP requirements; a P.Eng. license is an asset.

Skills

GMP Compliance
Quality Systems
Continuous Improvement
Investigation Management
CAPA Management
Root Cause Analysis
Risk Assessment
Regulatory Guidance
Pharmaceutical Manufacturing
Process Improvement
Quality Event Management
Data Trending
Cross-Functional Collaboration
Project Management
Facilitation
Problem-Solving

Benefits

Comprehensive Benefits
Bonus Eligibility
Professional Development Support
RRSP Program
Discounted Gym Memberships
Employee Assistance Program
Corporate Discounts
Employee Recognition Program
Social Events
Spirit Days

Visa sponsorship

Not detected in the job text

Keywords

Good Manufacturing Practices
Quality Management System
Continuous Improvement
Corrective And Preventive Actions
Deviation Investigations
Complaint Investigations
Audit Observations
Environmental Monitoring
Root Cause Analysis
Risk-Based Decision Making
Quality Risk Assessment
Regulatory Compliance
Health Canada
FDA
EU GMP
Pharmaceutical Manufacturing
Sterile Injectable Cartridges
Combination Products
Process Capability
Process Controls
Quality Metrics
Performance Trending
Change Assessment
Audit Readiness
Scientific Analysis
Problem-Solving Methodologies
Validation
Technical Services
Professional Engineer
Patient Safety

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