Production Supervisor

2 weeks ago

Windsor, Canada Catalent Full time

Production Supervisor

Position Summary

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

This position is located in Windsor, Ontario, one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a broad range of integrated formulation, manufacturing, analytical and packaging services to offer full-service turnkey solutions.

Reporting to the Production Manager, the Production Supervisor is responsible for assisting the manager in leading and coaching the shop floor production team in order to safely produce quality product in accordance to established criteria. The Production Supervisor will supervise the production team while empowering work teams to work at their capability level.

12 hour rotating continental shifts (Days and Nights)

The Role:

Promote productivity improvements. Meet daily production objectives and manage each shift with respect to production efficiencies, effectively utilizing corporate resources, labour, equipment, and materials.

Supervise a team of hourly employees involving a high level of engagement with team members. Deliver shift meetings as per pre-defined agenda.

Monitor and manage employee performance, including coaching and delivery of performance management actions.

Promote a “Patient First” culture within the production team.

Meet daily and long-term safety, quality, deliver (schedule attainment) and cost (efficiency, productivity) objectives.

Provide daily information on metric results per shift, through daily shift report and during Master Variance meeting.

Ensure the implementation of quality procedures, reinforce regulatory compliance with respect to Good Manufacturing Practices and ensure compliance with respect to company’s SOP’s (Standard Operation Procedures). Ensure that training and qualifications are current for all employees in the Shift/Department.

Other duties as assigned.

The Candidate:

High School Diploma, GED or equivalent is required.

Bachelor’s Degree in Life Sciences (Chemistry, Biology) or related field is preferred.

3+ years of experience in operations management or related field is required.

Experience working in a manufacturing, pharmaceutical and/or GMP facility an asset.

Demonstrated knowledge of pharmaceutical or food manufacturing processes.

Strong technical/engineering background.

Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

The employee is often required to sit and use their hands and fingers, to handle or feel and to manipulate keys on a keyboard.

Use of manual dexterity is required.

The employee is occasionally required to stand, walk, reach with arms and hands, bend, or twist, and to stoop, kneel, crouch or crawl.

Vision abilities required by this job include close vision.

There is also the potential exposure to chemicals.

Why You Should Join Catalent:

Comprehensive Benefit Package. (Health, Dental, Vision, & Life Insurance)

Group Retirement Savings- Registered Pension Plan (RPP) with employer contributions.

Employee Reward and Recognition Programs.

Opportunities for professional and personal development.

Catalent offers rewarding opportunities to further your career Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. 

personal initiative. dynamic pace. meaningful work.

Visit to explore career opportunities.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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