Processing Technologist I

Thermo Fisher Scientific•Whitby, ON

7d•CA$36,608 - CA$54,550•Onsite

About The Position

Safely manufactures high quality pharmaceutical products according to established schedules. This role involves processing/manufacturing products in accordance with written processing orders, preparing manufacturing areas and equipment, and cleaning processing equipment and rooms. The position ensures product quality meets established standards and adheres to Environmental Health and Safety (EH&S) and Good Manufacturing Practices (GMP) requirements. The role also requires maintaining a safe working environment and performing alternating or rotating shift work.

Requirements

High school diploma/General Educational Development (GED) Certificate is required.
Minimum 1 year experience in pharmaceutical, food or cosmetic related manufacturing.
Ability to maintain records of activities as instructed.
Ability to follow instruction with attention to detail.
Ability to lift up to 40 lbs.
Works well with limited supervision in a team environment.
Knowledge of Good Manufacturing Practices and safety standards.
Mechanical interest/aptitude.
Proficiency using Microsoft Office software applications.
Proficiency with the English language.
Follow all Environmental Health & Safety Policies and Procedures.
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.

Nice To Haves

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

Responsibilities

Process/manufacture products in accordance with written processing orders.
Prepare manufacturing areas and equipment for the production of pharmaceutical products.
Clean processing equipment and rooms in accordance with written Standard Operating Procedures (SOPs) and established Good Manufacturing Practices (GMP).
Ensure product quality meets the standards of Patheon, our clients, and applicable regulatory agencies including, but not limited to the Health Products and Food Branch Inspectorate (HPFBI), United States Food & Drug Administration (FDA), and European Medicines Agency (EMEA).
Follow the required Environmental Health and Safety (EH&S) and Good Manufacturing Practices (GMP) requirements.
Maintain a safe working environment and report potential hazards.
Perform alternating or rotating shift work.
Maintain records of activities as instructed.
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 SOP's and Good Manufacturing Practice (GMP).
Maintain workspace in a clean and orderly fashion.
Actively engage in and adhere to departmental systems in order 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.
Models 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.