Scientist I - Development Operations

Thermo Fisher Scientific•Whitby, ON

12d•Onsite

About The Position

Provide analytical support in the Laboratory Operations Department by following standard practices. Assist with method development and evaluation activities. Perform method validations and Research & Development (R&D) analytical testing. Make detailed observations and review, document, and communicate test results.

Requirements

B.Sc. in chemistry or a related field.
Previous experience in a science related environment.
Good understanding of basic chemistry and experience with common laboratory equipment and operation.
Good understanding of chromatographic separations.
Knowledge of qualitative and quantitative chemical or microbiological analysis.
Awareness of quality and regulatory requirements in the pharmaceutical industry.
Good problem-solving skills and logical approach to solving scientific problems.
Demonstrable interpersonal and communication skills (both oral and written).
Ability to read and interpret technical procedures and governmental regulations.
Ability to apply mathematical operations to such tasks as determination of test reliability, analysis of variance, and correlation techniques.
Works well independently and in a team environment.
Demonstrated computer proficiency with Microsoft Office programs.
Proficiency in the English Language.

Nice To Haves

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

Responsibilities

Document all experimental data in accordance with Attributable, Legible, Contemporaneous, Original and Accurate (ALCOA).
Independently carry out HPLC, dissolution and physical testing analysis testing following established procedures Analytical Methods & Standard Operating Procedures (SOPs).
Work Proficiency with Empower, NuGenesis, LIMS, SM, MS Word & Excel Software.
Perform basic troubleshooting to overcome system suitability failures.
Follow method validation protocols and carry out method validation bench work.
Support ECS (excipient compatibility study) testing.
Recognize and report unexpected or Out Of Specification (OOS) results immediately to the Supervisor and conduct laboratory investigations under direction.
Maintain a safe working environment, lab 5S and report potential hazards.
Perform alternating or rotating shift work (as required).
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.