Essential Functions:

• Document all experimental data in accordance with Attributable, Legible, Contemporaneous, Original and Accurate (ALCOA).

• Work proficiently with eDMS (electronic Documentation Management System), MS Word & Excel software.

• Prepare bulk solutions required for Scientists.

• Prepare raw data packages (notebook copies) for clients

• Provide support to Scientists by assisting with dissolution testing and sample preparation

• Perform simple in-process testing such as particle size distribution, tapped density and flow index

• Maintain a safe working environment and report potential hazards.

• Perform alternating or rotating shift work (as required)

REQUIRED QUALIFICATIONS

Education:

College Technician Diploma in Laboratory Technology or Related Field.

Bachelor of Science in Chemistry or related science (an asset)

Experience:

Previous experience with common laboratory equipment and operation (i.e. balance, pipettes).

Minimum 1 year of experience in a GMP Laboratory Environment (an asset).

Equivalency:

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

Knowledge, Skills and Abilities:

Good understanding of basic chemistry and experience with common laboratory equipment and operation. Awareness of quality and regulatory requirements in the pharmaceutical industry. Demonstrable interpersonal and communication skills (both oral and written). Ability to read and interpret technical procedures and governmental regulations. Able to provide physical testing support (appearance, KF, hardness & disintegration testing), an asset. Proficiency with the English language. Works well independently and in a team environment.

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 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.

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. Use of Personal Protective equipment may be required and may include any of the following: Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally.