Scientist I

4 weeks ago

Mississauga, Ontario, Canada Thermo Fisher Scientific Full time

Job Summary:

Thermo Fisher Scientific is seeking a highly skilled Scientist I to join our team in the Laboratory Operations Department. As a key member of our team, you will provide analytical support by following standard practices and assist with method development and evaluation activities.

Key Responsibilities:

  • Document all experimental data in accordance with ALCOA principles.
  • Independently carry out HPLC, dissolution, and physical testing analysis following established procedures and SOPs.
  • Work proficiently with Empower, NuGenesis, LIMS, SM, MS Word, and Excel software.
  • Perform basic troubleshooting to overcome system suitability failures.
  • Follow method validation protocols and carry out method validation bench work.
  • Support ECS testing.
  • Recognize and report unexpected or 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.

Requirements:

Education:

A degree in chemistry or a related field is required.

Experience:

Previous experience in a science-related environment is preferred.

Knowledge, Skills, and Abilities:

A good understanding of basic chemistry and experience with common laboratory equipment and operation is essential. Knowledge of chromatographic separations, qualitative and quantitative chemical or microbiological analysis, and quality and regulatory requirements in the pharmaceutical industry is also required. Good problem-solving skills, logical approach to solving scientific problems, and demonstrable interpersonal and communication skills are necessary. Ability to read and interpret technical procedures and governmental regulations, apply mathematical operations, and work well independently and in a team environment is also required.

Standards and Expectations:

FOLLOW ALL ENVIRONMENTAL HEALTH & SAFETY POLICIES AND PROCEDURES. Work collaboratively with fellow team members, model positive team principles, and partner to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality systems SOPs and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems to maintain a smooth and efficient workflow. 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 engaging 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 fields.

Physical Requirements:

Light physical effort and fatigue. Walks, sits, or stands for limited periods. May require occasional equipment operation, including keyboard equipment. Lifts light items for limited duration. Typically located in a comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as dust, fumes, or odors, temperature extremes, loud noise, strong drafts, or bright lights. Use of Personal Protective Equipment may be required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator on occasion.

Disclaimer:

This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as a comprehensive statement of work, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

Nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully align with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.

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