Thermo Fisher Scientific

Thermo Fisher Scientific

Posted via Workday

Validation Engineering Specialist II – Equipment Engineering

Posted Sep 3, 2026

Role at a glance

Salary
$56.4K – $84.6K/yr
Location
Canada - Mississauga
Work arrangement
On-site
Employment
Full-time
Education
Bachelor's

Spotted an issue?

We’ll check it against the original posting.

Log in to report

About the role

Original posting provided by Thermo Fisher Scientific

View original

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

As a Engineer Specialist II you provide specialized validation knowledge and information, which is directly required to support operations and clients. Complete all protocols related to the validation of equipment, processes and new products and review all finished reports prior to final approval. Ensure documents conform to all Patheon Standard Operating Procedures (SOPs), client requirements and Good Manufacturing Practices.


Essential Functions:

Prepare validation protocols and reports for process, packaging, or cleaning validation

Monitor and coordinate manufacturing execution and provide trainings on validation protocols

Perform data collection, statistical analysis and prepare summary reports

Monitor and coordinate swab sampling activities for cleaning validation

Prepare risk assessment, protocols and reports for Continued Process Verification program

Prepare protocols and reports for bulk hold studies, shipping studies and other additional studies as and when required

Interact with clients, project managers and other stakeholders to drive validation activities.

Maintain a safe working environment and report potential hazards.

Flexible to work extended hours or off-shifts based on project expectations (as required)

REQUIRED QUALIFICATIONS


Education:


Minimum post-secondary diploma in Chemistry, Engineering, Science or related field.
BSc in Chemistry or Engineering is an asset.

Experience:


Minimum 2-3 years experience in validation, process engineering or quality within the pharmaceutical/
biotechnological industry.
Previous experience in statistical analysis preferred.


Equivalency:


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

Knowledge, Skills and Abilities:


Strong written and oral skills. Detail oriented and organized, with a high degree of accuracy and thoroughness. Excellent interpersonal skills, communication and organizational skills. Strong judgment, decision making and trouble shooting skills. Ability to multi-task, meeting tight deadlines in a fast paced
environment. Mini-Tab and data analysis knowledge an asset. Demonstrated computer proficiency with Microsoft Office programs. Proficiency with the English Language.


Standards and Expectations:


Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members, modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality systems Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Effectively engage in and adhere to departmental systems to maintain a smooth and efficient workflow (visual management, scheduling systems, etc.). Be client and patient conscious at all times. Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for
system improvements and engage in problem solving. Model positive thinking and is open to change, motivating the team to adapt to shifts in priorities and new ways of working. Proactively identify areas for improvement in the execution of procedures. Communicate risks to timelines in a proactive manner. Consistently strives to improve skills and knowledge in related field.


Physical Requirements:


Position requires ordinary ambulatory skills and physical coordination sufficient to move about lab/lab 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 10-35 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, 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. Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally.
 
 

Compensation

The estimated annualized pay range for this position in Ontario is $56,400.00–$84,600.00.

Thermo Fisher Scientific

About the company

Thermo Fisher Scientific

Large Enterprise

Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.