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Scientist I, Analytical Operations

  • Job
    Full-time
    Entry Level
  • Science
    Research & Development
  • Whitby

AI generated summary

  • You need a B.Sc. in chemistry or related field, experience with lab equipment, knowledge of chromatography, strong problem-solving skills, and the ability to work well in teams and follow GMP standards.
  • You will conduct HPLC and dissolution testing, document data per ALCOA principles, troubleshoot issues, report OOS results, maintain lab safety, and collaborate with teammates to enhance performance.

Requirements

  • Required Qualifications
  • Education:
  • B.Sc. in chemistry or a related field, or equivalent experience.
  • Experience:
  • Proven experience with common laboratory equipment and operations.
  • Equivalency:
  • Equivalent combinations of education, training, and relevant work experience may be considered.
  • Knowledge, Skills, and Abilities:
  • Solid understanding of basic chemistry and chromatographic separations.
  • Knowledge of qualitative and quantitative chemical or microbiological analysis.
  • Awareness of quality and regulatory requirements in the pharmaceutical industry.
  • Strong problem-solving skills and a logical approach to scientific challenges.
  • Excellent interpersonal and communication skills, both oral and written.
  • Ability to read and interpret technical procedures and governmental regulations.
  • Capacity to apply mathematical operations to determine test reliability, analyze variance, and perform correlation techniques.
  • Demonstrated ability to work both independently and collaboratively in a team environment.
  • Computer proficiency with Microsoft Office programs.
  • Proficiency in the English Language.
  • Standards and Expectations:
  • Follow all Environmental Health & Safety Policies and Procedures.
  • Work collaboratively with fellow team members, modeling positive teamwork principles and partnering to meet project and departmental objectives.
  • Strictly adhere to Patheon quality systems SOPs and Good Manufacturing Practice (GMP).
  • Maintain workspace in a clean and orderly fashion.
  • Actively engage in departmental systems to ensure smooth and efficient workflow.
  • Be client and patient-conscious at all times.
  • Understand Key Performance Indicators and strive to improve team performance by identifying areas for system improvements and engaging in problem-solving.
  • Model positive thinking and openness to change, motivating the team to adapt to new priorities and methods.
  • Proactively identify areas for improvement in procedure execution.
  • Communicate risks to timelines proactively.
  • Consistently strive to improve skills and knowledge in the related field.
  • Physical Requirements:
  • Physical coordination and ambulatory skills are necessary for moving around lab/office locations. You should be comfortable standing, walking, stooping, kneeling, and crouching for long periods. You should also have good arm and hand dexterity and be able to use a keyboard and computer monitor. Safety equipment may be required, including glasses, shoes, a lab coat, gloves, an apron, and occasionally a respirator.

Responsibilities

  • Document all experimental data in accordance with Attributable, Legible, Contemporaneous, Original, and Accurate (ALCOA) principles.
  • Independently carry out HPLC, dissolution, and physical testing analyses following established Analytical Methods & Standard Operating Procedures (SOPs).
  • Demonstrate proficiency with Empower, NuGenesis, MS Word, and Excel software.
  • Perform basic troubleshooting to resolve system suitability failures successfully.
  • 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 and report potential hazards.
  • Perform alternating or rotating shift work as required to ensure flawless operations.
  • Follow all Environmental Health & Safety Policies and Procedures.
  • Work collaboratively with fellow team members, modeling positive teamwork principles and partnering to meet project and departmental objectives.
  • Strictly adhere to Patheon quality systems SOPs and Good Manufacturing Practice (GMP).
  • Maintain workspace in a clean and orderly fashion.
  • Actively engage in departmental systems to ensure smooth and efficient workflow.
  • Be client and patient-conscious at all times.
  • Understand Key Performance Indicators and strive to improve team performance by identifying areas for system improvements and engaging in problem-solving.
  • Model positive thinking and openness to change, motivating the team to adapt to new priorities and methods.
  • Proactively identify areas for improvement in procedure execution.
  • Communicate risks to timelines proactively.
  • Consistently strive to improve skills and knowledge in the related field.

FAQs

What is the work schedule for the Scientist I position?

The work schedule for the Scientist I position is standard hours from Monday to Friday.

What educational qualifications are required for the Scientist I role?

A Bachelor of Science (B.Sc.) in chemistry or a related field, or equivalent experience, is required for the Scientist I position.

What kind of experience is needed for this job?

Proven experience with common laboratory equipment and operations is required for this role.

What are the essential functions of the Scientist I position?

Essential functions include documenting experimental data, independently carrying out analyses like HPLC and dissolution, basic troubleshooting, maintaining a safe working environment, and performing rotating shifts as required.

What software proficiency is needed for this role?

Proficiency with Empower, NuGenesis, MS Word, Excel, and a solid understanding of basic chemistry is required.

Is there a need for physical activity in this job?

Yes, the position requires physical coordination and ambulatory skills, including standing, walking, and using laboratory equipment for extended periods.

What safety standards must be adhered to in this role?

Adherence to all Good Manufacturing Practices (GMP) and Safety Standards is mandatory in this role.

Are there opportunities for professional development?

Yes, the position encourages consistent striving to improve skills and knowledge in the related field.

How important is teamwork in this position?

Teamwork is essential, as the role requires collaboration with fellow team members to meet project and departmental objectives.

What should I do if I encounter unexpected results during testing?

You should immediately report unexpected or Out Of Specification (OOS) results to the Supervisor and conduct laboratory investigations under their direction.

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Mission & Purpose

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.