Scientific Technical Writer

2 days ago

Mississauga, Ontario, Canada Thermo Fisher Scientific Full time
Job Summary

We are seeking a highly skilled Scientific Technical Writer to join our team at Thermo Fisher Scientific. As a key member of our Development Laboratory, you will play a critical role in assisting with the preparation of analytical method validation protocols and reports, method transfer protocols and reports, analytical methods, and specifications.

Key Responsibilities
  • Assist with the preparation of technical documents, including method validation and transfer protocols, reports, analytical methods, and specifications.
  • Provide input on the generation of method transfer plans for incoming projects.
  • Document all experimental data in accordance with ALCOA principles.
  • Independently carry out HPLC, dissolution, GC, and physical testing analysis following established procedures and SOPs.
  • Work proficiently with Empower, NuGenesis, MS Word, and Excel software.
  • Recognize and report unexpected or 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.
Requirements
  • Bachelor of Science in Chemistry or a related science.
  • Minimum 3 years' pharmaceutical laboratory work experience.
  • Experience in preparation of technical documents.
  • Experience in laboratory testing and method validation.
Preferred Qualifications
  • Strong knowledge of analytical method validation requirements.
  • Excellent Good Manufacturing Practices, Good Laboratory Practices (GLP), International Conference on Harmonization (ICH), and United States Food and Drug Administration (FDA) compliance knowledge.
  • Proficient in Microsoft Office Suite (Word, Excel, and PowerPoint), Chemstation, and OpenLab.
  • Well-organized and detail-oriented.
  • Excellent interpersonal and communication skills (both oral and written).
  • Ability to work well independently and in a team environment with limited supervision.
  • Ability to prioritize multiple tasks.
  • Proficient in the English language.
Standards and Expectations
  • Follow all Environmental Health & Safety Policies and Procedures.
  • Work collaboratively with fellow team members, modeling positive team principles and partnering 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 in order to maintain a smooth and efficient workflow.
  • Be client and patient conscious at all times.
  • Understand Key Performance Indicators (KPIs) and strive to improve the performance of the team by identifying areas for system improvements and engaging in problem-solving.
  • Model positive thinking and be 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 strive to improve skills and knowledge in related fields.
Physical Requirements

The 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. Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally.

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