Technical Writer R&D - Maternity Leave
Job in
Markham, Ontario, Canada
Listing for:
SGS
Contract
position
Listed on 2026-02-15
Job specializations:
-
Research/Development
Research Scientist, Clinical Research
-
Pharmaceutical
Job Description & How to Apply Below
Position: Technical Writer R&D - 18-month Maternity Leave
Job Description The Technical Writer position is responsible for writing methods, protocols, reports, SOPs and evaluating compendia procedures as it impacts the pharmaceutical products or raw materials.
Manage medium and larger size projects and in collaboration with client and internal resources.Work with department manager and schedule projects according to projects prioritization and work with groups and functions to manage resources efficiently.Leading technical writer team for improvement initiatives and workload distribution.Responsible for supporting the scientists in R&D to prepare the documentation as required by clients, including follow up of change controls, maintaining the templates for laboratory documents.In addition, responsible for periodic review of the compendia changes and providing evaluation as it impacts the Raw Material, Finished Product and R&D groups within Analytical Operations.Working with chemistry laboratory personnel, write or review reports for method development, feasibility, transfer verification and validation projects.Working with chemistry laboratory personnel, write or review client methods for routine sample analysis as needed.Review various lab documents.Ensure timely review of compendia updates, such as USP, EP, JP.Document and communicate the compendia changes to impacted departmentsQualifications
Bachelor’s or master’s degree in Chemistry or a related science degree and two or more years related pharmaceutical experience.Must have previous research and development experience in a pharmaceutical setting or equivalentExperience minimum: 2 to 3 years experience in a Pharmaceutical LabMust be able to communicate clearly in English and have solid communication skills including grammar and composition.Have excellent interpersonal skills.Ability to work well with others & independently.Proven time management skills and a strong attention to detail.Knowledge of another language is an asset.Demonstrated understanding of cGMP regulations.
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