Job Description

Automation Specialist

Windsor, Ontario is 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.

Position Summary

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.

The Role

Maintain automation equipment following specific PM program as well as attend to breakdowns and troubleshoot related equipment.

Identify opportunities within the 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.

Work closely with the Automation Project Manager ensuring projects and improvements are implemented and commissioned as per schedule.

Actively monitor & validate the progress of vendors and contractors.

Create and execute validation documents on equipment and facilities under GMP documentation practices including change management system.

Must be able to work extended hours, weekends as needed, especially when problems occur or when deadlines must be met.

Other responsibilities as assigned.

The Candidate

Industrial Automation Diploma or Degree or in related field;

Alternatively, industry related technical background will be considered

Experience with PLC and recipe-based programming, willingness to train and keep

Experience in project engineering/management is considered an asset

Experience and familiarity with pharmaceutical manufacturing and relevant GMP practices

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.

Regular working hours: 8:00 AM - 4:30 PM or 8:30 AM - 5:00 PM with a 30-minute unpaid lunch.

Why you should join Catalent:

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

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

Paid Time Off Programs incl. vacation, banked time & personal time;

Employee Reward & Recognition programs;

Opportunities for professional and personal development & growth incl. 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.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

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.