Manufacturing Process Engineering

4 weeks ago

Trenton ON, Canada Raise Full time €80,000 - €90,000

Manufacturing Process Engineer · Full-time, permanent position
· of our key clients in the Life Sciences industry. They’re looking for skilled technical professionals like you to help complete
meaningful and impactful projects. Manufacturing Process Engineer (PE)

Manufacturing Engineering Manager

The primary function is to ensure the operation's performance integrity and compliance to customer expectations of all products manufactured at the company. The Process Engineer improves overall efficiency, quality, productivity, and cost of existing company processes, as well as being an integral part of the launch of new processes. The Process Engineer will prioritize their duties according to the SQDC mantra (Safety, Quality, Delivery and Cost) and will contribute to the safety of the team members by ensuring that equipment/processes are engineered to comply with all relevant safety and ergonomic standards.
Responsible for supporting all technical aspects of extrusion and molding production processes, which includes the definition, management, and continuous improvement of tooling, equipment and fixtures.
Will define the production process with enough detail that the production team may consistently meet the customer expectations and quality standards.
Will develop the process to meet the short and long-term needs of the customer in terms of quantity and delivery.
Process Engineer will use the following Engineering disciplines: Process Flow and Process Flow Analysis, Tooling Planning, Acquisition and Maintenance; PFMEA to establish process risk of failure
Maintain 5S standards alongside the production team.
Manufacturing Methods Engineering- New product introduction by developing manufacturing plans with work instructions
Provide engineering support to production lines through rework instructions, cost reduction and process improvements
Communicate information in an effective manner to aid in the advancement of a product from Concept Readiness to Implementation Readiness. This would include analyzing key data from a run and assembling an improvement strategy for the next run.
Ensure evidence of compliance to our internal policy and procedures. Draft, layout, and specify technical devices, parts, and equipment by providing documentation, detailed instructions, drawings, or specifications to define for others how devices, equipment, or structures are to be manufactured, assembled, modified, maintained, or used.
Provide technical input and direction during capital projects as it relates to machinery or tooling.
Utilize industry practices such as Lean, Six Sigma, and Project Management methodologies
Be role models in support of company objectives, policy and procedures and safety guidelines.

Embrace high-performance team principles
· BSc in Engineering with experience in new program/systems development.
· Has 2-3 years (min) of relevant professional experience, preferably in the medical device industry and regulatory compliance requirements.
· Process development, safe manufacturing processes, and facility design (AutoCAD preferably SolidWorks 3D)
· Installation Qualification (IQ), Operational Qualification (OP), and Product Qualification (PQ)
· Good Manufacturing Practices (GMP), Good Documentation Practices (GDP).
· Microsoft Office; Word, Excel, PowerPoint, Access, and Visio.
· Minitab Software and Statistical Process Control.

Excellent interpersonal skills, professional attitude, and the ability to interact with various individuals and present information effectively to an audience of various technical backgrounds.
· Data driver, customer-oriented, and not reluctant to take the lead.
· Quality Orientation
· Creative and Innovative Thinking
· Planning and Organizing
· Office and production floor environment, computer and desk work.

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