Technical Writer
Apollo Health & Beauty Care View all jobs
- Toronto, ON
- $65,000-75,000 per year
- Permanent
- Full-time
- Gym Access
- Dental insurance
- Health insurance
- Author and manage technical investigation reports related to deviations, OOS, and OOT results.
- Facilitate and document Root Cause Analysis (RCA) using structured methodologies (e.g., 5 Whys, Fishbone).
- Draft and support Corrective and Preventive Action (CAPA) documentation in collaboration with R&D, Quality Assurance, and Manufacturing.
- Prepare R&D Impact Assessments evaluating the effect of changes and/or deviations on product quality, safety, performance, and regulatory compliance.
- Prepare R&D Risk Assessments related to formulations, processes, equipment, raw materials, and scale‑up activities.
- Develop and maintain Raw Material Assessments supporting cosmetic, OTC, and natural products.
- Support raw material change evaluations and supplier‑related documentation as required.
- Generate Change Control documentation to support R&D activities, including formulation changes, process changes, equipment changes, and scale‑up activities.
- Generate technical documentation supporting transfer of R&D developed products to commercial manufacturing.
- Draft, review, edit, and maintain Standard Operating Procedures (SOPs), test methods, and technical reports.
- Ensure accuracy, consistency, formatting, and version control of R&D documentation.
- Support continuous improvement initiatives related to documentation processes and controls.
- Work closely with R&D Scientists, Product Development, Quality Assurance, Manufacturing, and Regulatory teams to capture technical information accurately.
- Translate complex scientific and technical data into clear, professional documentation.
- Perform other duties as assigned by the Director Technical Services in support of departmental and organizational goals.
- Bachelor’s degree in chemistry, Cosmetic Science, Pharmaceutical Sciences, Biology, or a related scientific discipline.
- Minimum 3–5 years of technical writing experience within the North American (USA & Canada) OTC, cosmetic, and/or natural products industry.
- Proven experience authoring investigation reports, RCA documentation, R&D Impact Assessments, R&D Risk Assessments, Raw Material Assessments, Change Controls, and technical transfer documentation.
- Strong understanding of cGMP‑regulated manufacturing environments.
- Working knowledge of Health Canada and FDA regulatory expectations for OTC and cosmetic products.
- Proficiency in Microsoft Office applications (Word, Excel, PowerPoint); experience with electronic QMS systems is an asset.
- Exceptional attention to detail and strong command of written English.
- Strong analytical, organizational, and time‑management skills.