Production Supervisor II - Night

Septodont; Cambridge; Presencial; CAD 86.000 - 105.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Excellent compensation/benefits

RRSP Program

Discounted gym memberships

Work life balance programs (EAP)

Corporate Discounts and PERKS

Employee recognition program

Social events and spirit days

Descripción de la vacante

Septodont’s Cambridge, Ontario site is seeking a Production Supervisor II to lead night shift operations, ensure GMP compliance, and drive process improvements. The role oversees staff, training, and documentation to meet production goals while maintaining safety and quality standards.

Onsite position with competitive compensation and benefits. Requirements include a science or engineering degree, 3+ years in pharma manufacturing, and 1+ year of supervisory experience.

Formación

• Minimum 3 years of related experience in pharmaceutical manufacturing
• At least 1 year of management experience
• Strong knowledge of Health and Safety legislation and employment standards
• Excellent interpersonal and communication skills

Responsabilidades

• Coordinate shift changeover ensuring materials and staff are ready
• Maintain presence on the production floor and resolve issues
• Ensure SOPs and GMP documentation are followed and deviations are addressed
• Support cross-departmental collaboration and training of staff
• Lead safety training and enforce safety rules across the team
• Participate in employee performance reviews and development plans
• Identify training gaps and coordinate new employee training
• Drive GMP and regulatory compliance to meet quality standards
• Complete batch records and shift reports for output and efficiency
• Model company values and standard business practices
• Perform other related duties as required

Conocimientos

People management

Leadership

Health & safety knowledge

Analytical skills

Communication skills

Organization skills

Problem solving

Customer service

Shift flexibility

Educación

Degree in Science or Engineering

Management training or certification (asset)

Descripción del empleo

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.