Process Specialist 2

General Information Reference 2025-2179 Category Operations - Engineering Job Title Process Specialist 2 Company Details Novocol Pharma is a growing contract development and manufacturing organization (CDMO) specialized in sterile injectable cartridges and combination product manufacturing. We strive for excellence and customer‑centricity to deliver value to global pharmaceutical clients through contract services for drug development and commercial manufacturing. With over 40 years in operation our team of 600 employees and modern facilities located in Cambridge Ontario provide a personalized and responsive experience for our customers. We are focused on serving our strategic partners and patients with quality integrity and value. Our employees are our number one asset We offer developmental opportunities excellent compensation and benefit programs discounted gym memberships work / life balance programs employee recognition social events and spirit days. We are a proud member of the Septodont group of companies. Septodont is a pharmaceutical and medical device company with a global leadership position in dental pain management. The group counts over 2000 employees worldwide and has remained a 100% family owned company for over 90 years. Our Cambridge facility serves as a significant manufacturing site within the Septodont group with high volume dental anesthetic production for a global customer base. We have an opportunity for a Process Specialist II. Job Summary The Process Specialist (II) is accountable to the Technical Services Manager for all activities related to project work and supporting process systems at Septodont Novocol Pharmaceutical Division. This includes supporting the ongoing business capital and regulatory items in any process related area of the company. Upon receipt of the Professional Engineer Designation (P. Eng.) incumbent may use the title Process Engineer. Responsibilities Manage and lead varied engineering assignments and projects from specification to turnover which may involve the interaction with multiple departments. Provide ongoing technical support in any process area as required. Liaise regularly with internal customers to understand their technical service needs. Identify opportunities for continuous improvement of equipment and process in order to minimize downtime, turnaround time and waste reduction while maintaining the highest standard of quality. Lead continuous improvement initiatives. Analyze and support validation for both qualification and requalification activities. Support relevant R&D projects and new product launches. Audit and approve protocol drafts and executed reports. Initiate independent studies, analyze and interpret data and make conclusions. Provide technical guidance to less experienced engineers and technicians working on common projects. Write commissioning and startup documentation. Design reformats and amend any Standard Operating Procedures (SOPs) as required. Prepare revises and interpret conceptual layouts, as‑built drawings and schematics for process and plant equipment. Maintain a high level of pharmaceutical compliance and regulatory safety in all aspects of work. Work harmoniously with all fellow employees. Perform other duties as required. Support the validation department in validation projects. Follow GMP and regulatory requirements and ensure quality standards are met. Observe and support all safety guidelines and regulations. Model the Company Mission, Vision and Values Statements policies and current standard business practices. Qualifications Education Bachelor of Engineering / Engineering Science degree is a requirement (Chemical or Mechanical preferred). Experience Minimum of 5 years experience in manufacturing environment preferably in pharmaceutical food / beverage or consumer packaging. Able to read and interpret architectural mechanical electrical and P&ID drawings / schematics. Excellent communication, interpersonal and organizational skills. Demonstrates initiative, problem‑solver, team player and self‑motivated. Has the ability to lead and take ownership on systems and projects. Experience in the use of PLCs / control systems on process equipment. Experience in AutoCAD, MS Project, Word, Excel and PowerPoint. Experience in a Lean Manufacturing environment is an asset. Professional Engineer designation preferred. Able to travel internationally in support of projects (up to 20%). Contract type Permanent Candidate criteria Minimum level of experience required. 6-10 years Job location North America, Canada, Cambridge Location 25 Wolseley Court N1R 6X3 Cambridge Required Experience Unclear Seniority Key Skills Hr Executive Recruitment, Internship, Information Technology Sales, Furniture, Administration Support Employment Type Full‑Time Experience years Vacancy 1 #J-18808-Ljbffr