Process Specialist II /Engineer II

At Septodont, a global leader in dental products and a key player in pharmaceutical development and contract manufacturing (CDMO), we are proud to work every day to improve patients’ health and well-being. Present in more than 110 countries, the Group relies on the energy, expertise, and passion of 2,600 employees. With 6 international production sites, Septodont combines industrial excellence, technological expertise, and innovation to meet the needs of healthcare professionals worldwide. In North America, our operations include facilities in Ontario, Quebec, and Pennsylvania. Our Cambridge, Ontario site is home to Novocol Pharma – a thriving center of innovation with over 40 years of expertise in sterile injectable cartridges and combination product manufacturing. Backed by a team of more than 675 dedicated professionals and modern facilities, we deliver high-quality, customer-focused solutions to partners around the world. Beyond our expertise, our people are our greatest strength. We foster a stimulating work environment where everyone can learn, grow, and build a career that reflects their aspirations, supported by continuous training and internal mobility. As a socially responsible company, we place diversity and inclusion at the heart of our development, convinced that they enhance collective performance and foster human experience. Joining Septodont means becoming part of a human-scale international group and contributing to a meaningful mission: improving health for as many people as possible. What if your next professional chapter started with us? We have an opportunity for a Process Specialist II / Process Engineer II . Candidates holding a Professional Engineering (P.Eng.) designation will be assigned the title Process Engineer II . Candidates without a P.Eng. designation will be assigned the title Process Specialist II . Job Summary The Process Engineer/ Process Specialist II is accountable for project execution and process system support across the organization. This role supports manufacturing operations, capital projects, process improvements, validation activities, and regulatory initiatives within a highly regulated environment. The successful candidate will provide technical expertise, lead engineering projects, drive continuous improvement, and ensure compliance with quality and regulatory requirements. Responsibilities Lead and manage engineering projects from specification through implementation and turnover. Provide ongoing technical support to manufacturing and process operations. Partner with internal stakeholders to understand and address technical service requirements. Identify and implement process and equipment improvements to reduce downtime, improve efficiency, and minimize waste. Lead continuous improvement initiatives. Support equipment qualification, requalification, and validation activities. Support new product introductions and relevant R&D initiatives. Review and approve protocols, technical reports, and validation documentation. Conduct technical investigations, analyze data, and provide recommendations based on findings. Provide technical guidance and mentorship to engineers, specialists, and technicians. Develop commissioning and start-up documentation. Create, revise, and maintain Standard Operating Procedures (SOPs). Prepare and interpret process layouts, as-built drawings, and equipment schematics. Maintain compliance with pharmaceutical quality, safety, and regulatory standards. Job Requirements Education Bachelor’s degree in Engineering or Engineering Science required. Chemical Engineering or Mechanical Engineering preferred. Experience and Skills Minimum 5 years of experience in a manufacturing environment, preferably within pharmaceutical, food and beverage, consumer products, or other regulated industries. Experience working in a Lean Manufacturing environment is considered an asset. Professional Engineering (P.Eng.) designation is preferred. Ability to read and interpret architectural, mechanical, electrical, and P&ID drawings and schematics. Strong communication, organizational, and interpersonal skills. Demonstrated initiative, accountability, problem-solving capability, and teamwork. Proven ability to lead projects and take ownership of systems and initiatives. Proficiency with AutoCAD, MS Project, Microsoft Word, Excel, and PowerPoint. Understanding of PLCs and process equipment control systems. What We Offer Excellent compensation and benefits package RRSP Program Discounted gym memberships Employee Assistance Program (EAP) Corporate discounts and perks Employee recognition programs Social events and spirit days Starting at approximately $100,000 CAD , with opportunity for increase based on qualifications and experience. Total rewards include comprehensive benefits, bonus eligibility, and professional development support. Work Authorization: Applicants must be legally authorized to work in the country where the position is based for the duration of employment. This position is not eligible for employer-sponsored immigration support. We are committed to diversity and inclusion, and thank all applicants in advance; however, we will be corresponding only with those selected for an interview. In accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act, we are committed to providing an inclusive and barrier free recruitment and selection process. Recruitment Fraud – please be aware of recruitment fraud. Novocol Pharmaceutical of Canada Inc. will never ask for banking information, money or any personal information up front. We will only respond to official applications submitted through our careers site. In addition, we will only use official corporate e-mail addresses ( or ) to communicate with applicants. Should you be contacted without submitting an application, please delete the message and advise your e-mail provider.