Senior Process Engineer

About CPL At CPL, we are passionate about pharmaceutical product development and contract manufacturing. Our aim is to be the top choice CDMO in the non‑sterile liquid and semi‑solid pharmaceutical products domain, and ultimately bring benefits to the customers using our manufactured products. For more than 30 years CPL has partnered with the world’s leading pharmaceutical companies to provide full‑service product development and manufacturing, singularly focused on innovation and efficiency. We recognize our employees are our number one asset and support their career growth. We also offer a benefits program which includes Health/Dental and Vision care, deferred profit‑sharing plan, paid time off, employee’s assistance program, work/life balance, employee recognition program, on‑site parking, discounted gym membership and wellness program. Job Summary Responsible for establishing and managing the scope, budget, schedule, construction and start‑up of various Capital Projects and Continuous Improvement Projects for CPL, ensuring that all company regulations and procedures are followed and that all work is done in a safe, timely and cost‑effective manner. Leads and manages the introduction of new products. Works with key stakeholders to facilitate the implementation of new products and technologies in manufacturing, packaging, and facilities. Job Responsibilities Working with members of the Engineering Team, assemble the appropriate project team to execute each project through concept development, scope definition and estimating, design, and construction execution. An important part of this role is the understanding of the end‑user requirements through ongoing consultation with representatives of those customer groups. Use mechanical, electrical and/or process systems expertise to work with individual Project Delivery Teams to ensure the appropriate commissioning, qualification and training plans with accompanying resources are in place to deliver efficient system start‑up. In cooperation with other CPL project leadership team members, ensure that all systems are in place to ensure due diligence in design and construction procurement/execution and project cost and schedule controls. Ensure that all work is performed in full compliance with established CPL regulations and standards including, but not limited to, CPL‑safety policies and procedures, cGMP, building code and MOL/MOE requirements. Lead the development and ongoing maintenance of engineering design and construction standards and ensure compliance on all project executions. Support as required the trouble‑shooting and problem resolution of facility systems and operational equipment. Ensure all necessary permits, as required by the current codes, are obtained and that any necessary inspections are scheduled. Lead and support the development and execution of F.A.T‑, commissioning and validation requirements and associated documentation for work assigned, as required. Actively supports the Business Development (BD) team in the introduction of new products and modifications of existing products. Provide technical support to BD on creation of new routing and provide process flows for the manufacturing and packaging of new products and/or modification of existing products. Leads customer process optimization and investigations, equipment selection and customer audits and visits. Assist the Operations Management Team in meeting corporate goals and objectives. Provide mentorship, coaching, and technical guidance to engineering students and Level I and II Process Engineers. Perform other related duties as required. Required Qualifications Post‑secondary education in Engineering/Technology in the Province of Ontario or equivalent experience. Experience Minimum 10 years’ experience in leading the design/construction of capital and continuous improvement projects in a fast‑paced, high‑technology, team environment, preferably in the pharmaceutical or food industry, with at least 3 years in leadership experience. Knowledge, Skills, Abilities In depth technical understanding of relevant unit operations in the pharmaceutical industry, their capabilities and associated processes. High preference for liquid and semi‑solid dose operations. Proven track record in managing major capital and CI projects in a team environment “on time and on budget”. In depth understanding of automated / integrated production equipment and computerized systems. In depth knowledge in the qualification and validation of equipment, facility and processes. Proficiency in the creation of qualification documentation with minimal supervision. Experience in managing customers, vendors, consultants and contractors. Proven leadership capabilities/competencies, and ability to manage teams and reach objectives without formal reporting relationships. Knowledgeable in the numerous regulatory aspects of capital construction, including the Occupational Health and Safety Act, the Ontario Building Code, the Boiler and Pressure Vessel Act, etc. PEO (Professional Engineer of Ontario) designation eligibility – P. Eng. preferred. Strong interpersonal and communication skills. Strong organizational skills. Fluent in Microsoft Project, Word, Excel. Physical Demands / Working Conditions Office environment (in person) and support in production area. Occasional off‑shift hours as needed to support production schedule. Equal Opportunity Statement CPL is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. CPL is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us. We thank all applicants for their expression of interest; however, only those selected for an interview will be contacted. No phone calls or agencies please. Seniority level Mid‑Senior level Employment type Full‑time Job function Management and Manufacturing Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Contract Pharmaceuticals Limited by 2x. Mississauga, Ontario, Canada CA$65,000.00‑CA$85,000.00 3 weeks ago #J-18808-Ljbffr