Process Technician Position Summary: Work Schedule: Monday-Friday 8 AM-4:30 PM; potential to transition to 12-hour shifts in the future This position is 100% on-site at the Adair 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. Reporting to the Production Supervisor, the process technician will develop skills in their area and secondary area, they will know all basic tasks, be a specialist in their main area and learn skills in a support area. The process technician will mentor trainee technicians in areas where support is needed and assist other process technicians and lead technicians in maintaining production schedule via providing support in areas they are trained in. The Role: Minimise equipment downtime and improve equipment availability by being accountable for delivering and reducing machine turnaround time. Ensure the team consistently sets and upholds site safety best practices by demonstrating zero-tolerance behaviors, continually challenging and raising safety standards, and eliminating risk to employees, products, and the environment through active participation in safety and accident investigations and completion of high-quality, current risk assessments. Ensure team consistently sets site quality best practices by demonstrating zero defect behaviour, continually challenging and raising Quality standards. Ensure batch manufacturing records are accurately completed in real time to support timely documentation approval, with processes and procedures including online and in‑process quality checks—followed rigorously to deliver consistent, high‑quality products, while ensuring all team members adhere to SOPs and comply with individual cGMP responsibilities to prevent any deficiencies. Carry out specific targeted training as required, and ensure Compliance Wire training requirements are carried out within specified due dates Recommend improvements to the batch manufacturing process, SOP’s to increase process efficiency and effectiveness and maintain 5S and continuous improvement activities. Ensure that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Catalent values. Perform other duties as assigned. The Candidate: High School Diploma, GED/CAEC and/or educational credential assessment (ECA) is required. 2 years or more of experience in manufacturing environment is preferred, GMP work experience preferred, Pharmaceutical Manufacturing experience is an advantage. This role is required is to be clean shaven to wear a respirator, which is deemed mandatory to meet Health & Safety requirements. Good math skills and Capable of operating related computer applications. Ability to work independently, as required and complete daily activities and work cooperatively in teams, communicates clearly and has effective listening skills. Good standard of oral and written English and ability to follow written instructions. Able to complete written batch records. Candidates with non-Canadian credentials must provide an evaluation confirming the Canadian equivalency of the credentials as determined by the Alliance of Credential Evaluation Services of Canada (ACESC) such as WES. This position does not qualify for sponsorship. Frequent standing, walking, climbing ladders/steps, reading written documents, and use of a computer monitor, as well as talking and listening; occasional stooping, kneeling, crouching, bending, carrying, reaching with hands and arms; occasional lifting and/or moving up to 25 kg; and may be exposed to inclement weather or required to work in environments that require the use of protective gear and heightened awareness of personal and others’ safety. Pay: The start hourly rate for this position is $26.93/Hr. Catalent is a global employer, and this compensation 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 Paid Time Off 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 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. 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.