Production Supervisor I

General information

Reference

Category

Operations - Manufacturing

Job Title

Production Supervisor I - Weekend Days

Company Details

Novocol Pharma is a growing contract development and manufacturing organization (CDMO), specialized in sterile injectable cartridges and combination product manufacturing. We strive for excellence and customer-centricity to deliver value to global pharmaceutical clients through contract services for drug development and commercial manufacturing. With over 40 years in operation, our team of 600 employees and modern facilities, located in Cambridge, Ontario provide a personalized and responsive experience for our customers. We are focused on serving our strategic partners and patients with quality, integrity, and value.

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.

We are a proud member of the Septodont group of companies. Septodont is a pharmaceutical and medical device company with a global leadership position in dental pain management. The group counts over 2000+ employees worldwide and has remained a 100% family owned company for over 90 years. Our Cambridge facility serves as a significant manufacturing site within the Septodont group with high volume dental anesthetic production for a global customer base.

We have an opportunity for a Production Supervisor I.

Job Summary

SHIFT: Weekend Day Shift
NUMBER REQUIRED: 1
Grade 9

The due date for internal applicants to apply for this role is November 21, 2025.

The Production Supervisor I is an entry level position where the successful candidate will be provided with on-the-job training and coaching to develop into the Production Supervisor II role.  The Production Supervisor I is responsible for assisting the Production Supervisor II with the day-to-day operations including employee performance, machine efficiency, and improvement initiatives to facilitate enhanced productivity.

The successful candidate will follow a structured training program that is focused on Standard Operating Procedures, Good Manufacturing Practices, learning and understanding the pharmaceutical manufacturing environment, and developing into an effective leader who demonstrates key leadership competencies with a focus on Septodont's vision, mission, and values.

Responsibilities

 PRIMARY DUTIES AND RESPONSIBILITIES:

· Supports coordinating shift changeover by ensuring:

o    Machinery and human resources are optimal and report any deficiencies in a timely fashion.

o    Availability of components and supplies.

o    The Production Areas are clean and organized.

· Maintains a visible presence on the production floor and assists in resolving issues related to production/output.

· Assists with Monitors job duties to ensure that all pertinent SOPs are followed and all activities are documented properly.

· Works with the Production Supervisor II to issue, investigate and rectify Quality Assurance deviations, including:

o    Revising departmental SOPs and other GMP documents.

o    Fixing documentation errors and coaching related operators on documentation practices.

· Maintains a high degree of co-operation with other departments and participates 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 the Human Resources Department, support Employee Relations activities such as: assisting in the completion of employee performance reviews, monitoring performance improvement initiatives and guiding employee improvement action plans, supporting the administration of disciplinary action, and guiding conflict resolution by assisting in the investigation of employee complaints and recommending suitable resolutions.

· Coordinates new employee training and other training requirements of production staff through reviewing identified training gaps and supporting cross training plans.

· Ensures GMP and regulatory requirements and confirms quality standards are met.

· Completes Batch Record Reviews and daily shift reports for output, efficiency, downtime and other required matrices.

· Models the Company Mission, Vision and Values Statements, policies, and current standard business practices.

· Performs other related duties as required.

Qualifications

BASIC REQUIREMENTS:

Education

· University degree in a Science or Engineering related discipline.

Experience

· Demonstrated ability to work as part of a team, building positive relationships with team members.

· Effective communication skills both verbal and written with the ability to delegate and to work within interdepartmental teams.

· Excellent customer service and troubleshooting skills.

· Ability to motivate and to influence.

· Proven analytical and problem solving skills with the ability to make recommendations. 

· Demonstrated organizational skills with the ability to manage multiple priorities.

· Must be able to attend all shifts.

What we offer

Excellent compensation/benefits package.

Bonus and reward programs

Discounted gym memberships

Programs supporting work life balance

Employee recognition program

Professional and personal development programs

social events and spirit days

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 or )  to communicate with applicants. Should you be contacted without submitting an application, please delete the message and advise your e-mail provider.

Contract type

Permanent

Job location

North America, Canada, Cambridge

Location

25 Wolseley Court N1R 6X3 Cambridge

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