Production Automation Specialist
7 days ago
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.
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.
Reporting to the Engineer & Maintenance Manager, the Automation Specialist will be the primary point-person responsible for planning, executing, and delivering automation and process simplification projects on time, within budget, and in accordance to specifications at both Ontario softgel sites.
Efficient delivery of project deliverables, effective quality control, and clear communication of expectations to stakeholders, and upward reporting to senior management are critical tasks that must be performed throughout each project's lifecycle.
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.
Monday - Friday; Identify opportunities within the manufacturing plant for enhanced automation to reduce costs, increase repeatability and significantly improve quality and compliance.
Full ownership of the programming aspect of all vision, PLC, and recipe-based process equipment in manufacturing ensuring all products are qualified to run at product launch and maintained through product life cycle.
Develop, execute, and monitor project schedule to deliver projects under tight timelines and prepare and issue requests for quotation and scope of work documents.
Actively monitor & validate the progress of vendors and contractors and create and execute validation documents on equipment and facilities under GMP documentation practices including change management system.
Provide timely, formal, and professional updates on project status including Scope / Schedule / Budget and identify and train a backup employee to cover automation needs in times when needed.
Industry related technical background will be considered an asset.
Experience with PLC and recipe-based programming is required.
Experience in project engineering/management is considered an asset.
Experience and familiarity with pharmaceutical manufacturing and relevant GMP practices is an asset.
Strong verbal and written communication skills (English)
CAD Experience (AutoCAD, SolidWorks, Cadkey) is considered an asset.
MS Office (Word, Excel, Project, etc.)
Technical writing ability.
Knowledge of general construction processes / ESA approvals / PSR events / TSSA regulations / building codes are an asset.
Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance)
Group Retirement Savings –Registered Pension Plan (RPP) with employer contributions.
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 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 .
Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
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