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Process Engineering Specialist

2 months ago

Vaughan, Ontario, Canada Cheme Engineering Full time

Overview

This position offers a unique chance to become part of a vibrant process engineering firm that caters to a wide array of sectors, such as pharmaceuticals, biologics, science and technology, as well as food and beverage. Our organization comprises a team of committed professionals who strive for excellence, providing an environment where individuals are both challenged and supported. We prioritize the growth of our employees through career development, training, and mentorship, understanding that our achievements are intertwined with those of our clients and the potential of our team members.

Role of Process Engineers

Process Engineers at Cheme are specialists who undertake engineering responsibilities, which include the selection and sizing of equipment, performing engineering calculations, creating drawing and specification packages, preparing capital budgets, and implementing systems in accordance with good manufacturing practices (GMP), good documentation practices (GDP), regulatory guidelines, and safety and environmental controls.

These engineers are accountable for the execution of projects, prioritizing client service, and leveraging their leadership and project management skills to ensure timely delivery of projects that meet specifications and budget constraints. They facilitate project deliverables by effectively coordinating with client stakeholders, equipment suppliers, and contractors, fostering successful project completions and enduring partnerships with clients.

Key Responsibilities

  • Act as the primary engineering liaison with clients for designated systems and equipment.
  • Evaluate and ensure compliance of selected equipment, components, and instrumentation with client standards and their integration with existing systems.
  • Identify and review process and equipment system boundaries.
  • Assess engineering calculations, equipment sizing, P&IDs, layout drawings, general arrangement drawings, and equipment data sheets.
  • Examine engineering specifications, including user requirements specifications, functional specifications, and detailed design specifications.
  • Review BIM Models and approve shop drawings.
  • Analyze commissioning and qualification protocols.
  • Assist in risk assessments related to safety and quality.
  • Support startup and execution during the CQV phase.
  • Prepare comprehensive reports.
  • Oversee and coordinate equipment installation and startup.
  • Conduct field troubleshooting at client sites.
  • Engage in work at client locations.

Qualifications

  • Minimum of 5-7 years of experience in mechanical, chemical, process engineering, process development, or technology transfer.
  • Bachelor's degree in Applied Science from a recognized North American university.
  • Familiarity with Kneat electronic validation software is advantageous but not essential.
  • Ability to work independently within a cross-functional team.
  • Strong organizational and multitasking skills.
  • Ability to perform well under pressure.
  • Exceptional communication and interpersonal skills are essential.
  • Personable demeanor.
  • Proficient written and oral communication skills, with the ability to articulate technical concepts clearly.
  • Curiosity about various technologies and software, with a self-driven desire to gain proficiency.
  • Proficient in Microsoft operating systems and Microsoft Office Suite for document preparation.
  • Valid driver's license and vehicle ownership.
  • Multilingual abilities are an asset but not mandatory.

Core Competencies

  • Mechanical, Chemical, and Process engineering expertise with 5 to 7 years of relevant experience.
  • Experience in executing engineering tasks, including:
    • Process engineering calculations, equipment sizing, specifications, flow diagrams, and P&IDs.
    • Design engineering of mechanical piping, skids, components, and layouts.
  • Ability to comprehend, verify, and annotate engineering design documents (P&IDs, electrical drawings, functional specifications, design specifications, etc.).
  • Understanding of cGMP, GDP, and regulatory requirements (FDA, Health Canada, EU) relevant to the pharmaceutical and biotech industries.
  • Familiarity with automated Process Control Systems (PCS), Distributed Control Systems (DCS), Manufacturing Execution Systems (MES), PLCs, and Historian systems in a manufacturing context.
  • Knowledge of validation using a risk-based approach per ASTM E2500 Standards is a plus.
  • Capability to train and develop junior staff.
  • Proficient in English, with the ability to communicate effectively with clients.
  • Adept at interacting with clients and others in a professional and courteous manner.
  • Competent in using Microsoft operating systems and Microsoft Office Suite for document preparation.

Benefits

  • Comprehensive Healthcare Plan (Medical, Disability, Dental & Vision).
  • Paid Time Off Benefits.
  • Flexible Work From Home options.
  • Opportunities for Training & Development.
  • Bonus, Awards, and Gifts.
  • Employee Assistance Program offering Counseling services.