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Production Supervisor
Catalent Company
Source: Headcount Labs · original listing ↗
Job data: Headcount Labs, ODbL 1.0. Job descriptions belong to their employers.
Posted 26 oct.
About this role
About Site The newly launched manufacturing facility on Adair Blvd marks a pivotal expansion of Catalent’s Zydis® technology, a globally renowned, fast-dissolve oral dosage form that has transformed the lives of millions of patients worldwide. This is your opportunity to join a dedicated team at the forefront of pharmaceutical manufacturing. At Adair, you’ll play a vital role in the startup of a site built for innovation and excellence, from installation and qualification to regulatory approval and commercial manufacturing. Position Summary We have an opportunity for a Production Supervisor to join our team reporting directly to the Site Director. This role plays a key part in ensuring the safe and efficient production of high-quality pharmaceutical products while maintaining strict compliance with regulatory standards. You will lead and empower your team to achieve operational excellence and continuous improvement. This position offers the chance to contribute to a growing facility dedicated to innovation and quality. Shift: Monday-Friday 8 AM-4:30 PM; Transition to 12-hour shifts in the future Location: Adair, ON 100% Onsite The Role * Meet daily production objectives and manage each shift to ensure production efficiency, optimizing the use of resources, labor, equipment, and materials. * Supervise a team of hourly employees with a strong focus on engagement and performance. * Ensure compliance with safety, quality, efficiency, uptime, cost, and Quality Control objectives, as well as adherence to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). * Assist in troubleshooting and investigations to address off-standard results. * Maintain safety, health, and environmental procedures, identifying and correcting potential issues while driving continuous improvement through Risk Assessment strategies. * Schedule manpower, machinery, and materials to meet or exceed budget requirements, resolving work problems and recommending productivity and quality improvements. * Work extended hours or weekends as needed to meet deadlines or address operational issues. * Perform other duties as required. The Candidate Minimum Requirements * High School Diploma, GED/CAEC and/or educational credential assessment (ECA) is required. * Minimum 3+ years of experience leading and supervising a team in a manufacturing environment, ensuring safety, quality, and productivity. * Excellent leadership, communication, and interpersonal skills to manage a diverse workforce and foster a culture of continuous improvement. * Must be clean shaven to wear a respirator, as required by Health & Safety standards. * 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. * Currently, Catalent participates in the Ontario Immigrant Nominee Program (OINP) on a limited basis. * Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency through the Alliance of Credential Evaluation Services of Canada (ACESC), such as World Education Services (WES). * The employee's role frequently involves sitting and utilizing hands and fingers for tasks such as handling, feeling, and keyboard manipulation, necessitating manual dexterity. Occasionally, the position requires standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, alongside close vision capabilities and potential exposure to chemicals. Preferred Skills & Background * Bachelor’s degree in a relevant field such as Life Sciences, Engineering, or a related discipline preferred. Equivalent education and experience may be considered. * Strong commitment to workplace safety and a thorough understanding of occupational health and safety regulations in Ontario. * Strong analytical and problem-solving skills to identify and resolve production issues, optimize processes, and drive continuous improvement. * Excellent written and verbal communication skills to collaborate effectively with cross-functional teams including quality control, supply chain, and engineering. * Strong organizational and time management skills to prioritize tasks, allocate resources effectively, and meet production schedules. * Proficiency in Microsoft Office Suite (Outlook, Excel, PowerPoint, Word). Pay The final salary offered to a successful candidate may vary within this range $65,000 – $80,000, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a global employer, and this salary range does not reflect positions that work in other countries. 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 & Recognition programs * Opportunities for professional and personal development & growth including tuition reimbursement 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 [Catalent Careers](https://careers.catalent.com/us/en) 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 [DisabilityAccommodations@catalent.com](mailto:DisabilityAccommodations@catalent.com). 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. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.