Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Discover Impactful Work:

Responsible for driving automation & controls related capital projects for pharmaceutical manufacturing equipment. This includes supporting the definition of system standards, reviewing vendor proposals, and managing third party integration partners. The successful candidate will also act as on-site escalation support for maintenance regarding automation and controls related issues.

Day in the life:Develops, plans and executes automation and controls related capital projects through the entire project lifecycle (scoping, design, procurement, construction, installation, and commissioning)Supports the automation and controls workstream in capital projects led by the Capital Engineering team.Supports projects through Commissioning, Qualification, and Verification and ensure all automation and controls project deliverables are achieved.Contributes to the definition, implementation, and maintenance of standards and SOPs for the site as it related to automation and controls.Reviews URS, SDS, HDS, electrical drawings and specifications, piping and instrumentation diagrams, and I/O lists.Reviews, analyzes, and revises existing programs as required for updates/upgrades to PLC logic.Supports Quality investigations regarding electronic data and equipment reliability.Offers escalation support for the Maintenance Equipment Services Team to provide technical support post-equipment installation which includes regular, off-shift and weekend coverage as required.Prepares training manuals and deliver technical training to Operations and Maintenance team members for new systems.Creates and manages Change Control process for entirety of project execution.Gathers and analyzes data and technical information to support Continuous Improvement (PPI) and Capital Projects.Supports Factory Acceptance Testing (FAT) at OEM facilities and Site Acceptance Testing (SAT) at ThermoFisher Scientific facilities.Ensures all equipment and work performed by or on behalf of the company complies with all governing laws, practices, codes, and regulations.Contributes to the development of the Pharma 4.0 roadmap for the site and the standardization of process and packaging equipment solutions for common applications Ensure that third-party vendors and contractors under your supervision receive detailed safety instructions before they start work.Ensure that third party vendors or contractors under your supervision work in compliance with health and safety-related legislation and company’s health and safety program.Mentors and coaches junior team members within the Automation and Controls Engineering Department.Travel within the local ThermoFisher Scientific sites as well as internationally to supplier locations and industry trade shows may be required.Performs alternating or rotating shift work (as required)

Keys to success:

Education:

Minimum Bachelor’s degree in Engineering. Specialization in Electrical, Mechatronics, or Industrial Automation / Instrumentation, preferred.

Professional Engineer Designation is an asset.

Experience:

Minimum 3 years experience in an automation and controls related position in a GMP and/or regulated environment.

Experience with Allen Bradley Systems such as ControlLogix and PlantPAx

Experience leading capital automation and controls projects

Equivalency:

Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities:

Ability to read, analyze and interpret electrical schematics, control panel drawings, technical procedures, process & instrumentation drawings, engineering drawings, and government regulations. Skilled in PLC /HMI Programming, industrial networks configuration/troubleshooting. PlantPAx DCS, Kepware OPC, and Ignition SCADA software certifications are an asset. Proficiency in GMP systems. Understanding of Validation & IQ/OQ/PQ program along with 21 CFR Part 11. Strong judgment, decision making abilities, trouble shooting and thinking-out-of-the-box skills. Excellent organizational, verbal and written communication skills. Solid computer experience with MS applications (Project, Word, Excel). Knowledge of AutoCAD. Proficiency with the English language.

Physical Requirements:

Position requires ordinary ambulatory skills and physical coordination sufficient to move about manufacturing/office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of up to 40 pounds; arm, hand and finger dexterity; visual acuity to operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Usually in a comfortable environment but with regular exposure to factors causing moderate physical discomfort from such things as dust, loud noise, bright lights, fumes or odour. Use of Personal Protective equipment is required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

OTHER

Relocation assistance is NOT providedMust be legally authorized to work CanadaMust be able to pass a comprehensive background check

Compensation

The salary range estimated for this position based in Canada is $69,400.00–$104,050.00.