Production Supervisor (Night Shift)

Shift: Night Shift , Monday-Friday, 11:00pm - 7:30am

Vacancy Status : This position will be vacant in March 2026

AI Disclosure in Hiring : We do not use artificial intelligence to screen, assess, or select applicants

Job Summary

Reporting to the Production Manager, the Production Supervisor leads the day-to-day management of all production activities for the morning shift at the Beaverdale, Cambridge. The Supervisor oversees all production-related, people, safety, quality delivery and cost activities, handles inventory management of critical production supplies, and leads continuous improvement projects to enhance compliance, productivity and costs within the facility. Reporting into the Production Supervisor will be hourly production employees in various classifications.

Key Role Specific Responsibilities

• Lead and manage production to established specifications within a sterile and aseptic work environment, ensuring compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), safe work practices, and other company policies and procedures.
• Inventory management of critical supplies to ensure production needs are met.
• Maintain and optimize regular management processes (production schedules, daily performance metrics, communication and reduction in unplanned downtime, scrap, rejects, etc.) and make recommendations and take actions for improvements.
• Motivate and develop employees via coaching, positive influence, team building, daily communication and accountability management, with a view to maintain and improve processes and performance; and implementing projects and standard operating practices to reach business and team objectives.
• Facilitate training and development of all production employees, ensuring they have the skills, knowledge and competence to carry out their duties efficiently, effectively and safely and to cGMP/GDP standards.
• Ensure all deviations from validated processes and procedures are reported, investigated with actions in accordance with company requirements and timelines.
• Ensure safety, health and environmental procedures are given due priority. Identify, investigate, correct and document potential environmental and safety problems. Ensure corrective actions are implemented and adhered to on a daily basis.
• Control and oversee environmental compliance and waste handling, storage and disposal for the facility, ensuring compliance with all regulations.
• Develop solid respectful relationships with direct reports, department managers and co-workers in various departments.
• Collaborate with other departments and share knowledge for continuous improvement and to meet product quality standards.
• Respond to all inquiries both internal and external in a timely manner.
• Attendance management, including absenteeism.
• Payroll - ensuring all hours worked are accounted for in the ADP time-keeping system.
• Other duties as assigned.

Competencies Required for the Role

• FOSTERING COLLABORATION/TEAMWORK - the ability to work jointly with others or together especially in an intellectual endeavor; the ability and desire to work cooperatively with others on a team; as a team leader, the ability to demonstrate interest, skill, and success in getting groups to learn to work together. Builds partnerships for global performance. Respects others.
• JUDGEMENT - the ability to make considered decisions or come to a sensible conclusion.
• PROCESS IMPROVEMENT - involves the business practice of identifying, analyzing, and improving existing processes to optimize performance.
• PLANNING - the process of thinking about and organizing the activities required to achieve a desired goal.
• INITIATIVE - Identifying what needs to be done and doing it before being asked or before the situation requires it.

Requirements

• 5+ years of supervisory experience in a production/manufacturing environment.
• At least 2 years of experience in aseptic manufacturing environment would be considered an asset.
• University or College degree required.
• Strong working knowledge of cGMP, FDA and Health Canada regulations would be considered an asset.
• Working knowledge of the Ontario Occupational Health and Safety Act.
• Exposure to problem solving & continuous improvement methodology and practices.
• Strong technical aptitude.
• Self-starter with the ability to provide solid leadership to a diverse team.
• Proven ability to build relationships.
• Strong written and verbal communication skills.
• Strong analytical and problem-solving skills.
• Strong interpersonal skills, professional attitude and the ability to interact with various individuals.
• Computer literate in the MS suite of programs.
• Manufacturing experience at a supervisory level in a pharmaceutical environment.
• Competitive vacation policy effective upon hire.
• 13 paid holidays.
• Defined Contribution Pension plan with employer matching 5%.
• Employee Assistance Program.
• Expected Salary Range: $82,000 per year.

Equal Opportunity & Accessibility. At Bimeda we are committed to fostering an inclusive, barrier-free and accessible environment. Part of this commitment includes arranging accommodations to ensure an equitable opportunity to participate in the recruitment and selection process. If you require an accommodation, we will work with you to meet your needs. We are committed to an inclusive and accessible recruitment process. We are an equal opportunity employer and assess candidates based on skills and experience. Recruitment records are retained in accordance with Ontario law.