Technical Writer
Apollo Health and Beauty Care
Benefits:
Gym Access
Dental insurance
Health insurance
We're Hiring!
The
Technical Writer
reporting to Director of Technical Services is responsible for authoring, reviewing, and maintaining accurate, clear, and compliant technical documentation to support Apollo Health & Beauty Care's research, development, technology transfer, and commercial manufacturing activities. This role plays a critical part in ensuring that R&D outputs are well documented, scientifically justified, traceable, and audit ready in accordance with internal Quality Management System (QMS) requirements and applicable regulatory expectations.
The position requires an experienced technical writer with demonstrated expertise in the North American (FDA & Canada) cosmetic, OTC, and natural products industr, capable of independently preparing complex investigation reports, risk assessments, and change control documentation supporting laboratory development through to commercial batch production.
Investigations, Root Cause Analysis & CAPA
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.
R&D Impact & Risk Assessments
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.
Raw Material Assessments
Develop and maintain Raw Material Assessments supporting cosmetic, OTC, and natural products.
Support raw material change evaluations and supplier‑related documentation as required.
Change Control & Technical Transfer
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.
Technical Documentation & SOPs
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.
Cross-Functional Collaboration
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.
Other Duties
Perform other duties as assigned by the Director Technical Services in support of departmental and organizational goals.
JOB REQUIREMENTS
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.
Apollo Health & Beauty Care Ltd. will ensure accommodations are available in consultation with candidates during all stages of the recruitment process. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Duties outlined in this job description may not be all-inclusive, and can be modified at any time if requested by management. Apollo is committed to providing accommodations for people with disabilities in all parts of the hiring process. Apollo will work with applicants to meet accommodation needs that are made known in advance.
We thank all applicants for their interest however only those meeting the minimum qualifications will be interviewed.
Vacancy Status:
This posting represents an
existing vacancy, and we are actively recruiting to fill this position.
Job Criteria
Seniority level:
Mid-Senior level
Employment type:
Full-time
Job function:
Marketing, Public Relations, and Writing/Editing
Industries:
Manufacturing
#J-18808-Ljbffr
Gym Access
Dental insurance
Health insurance
We're Hiring!
The
Technical Writer
reporting to Director of Technical Services is responsible for authoring, reviewing, and maintaining accurate, clear, and compliant technical documentation to support Apollo Health & Beauty Care's research, development, technology transfer, and commercial manufacturing activities. This role plays a critical part in ensuring that R&D outputs are well documented, scientifically justified, traceable, and audit ready in accordance with internal Quality Management System (QMS) requirements and applicable regulatory expectations.
The position requires an experienced technical writer with demonstrated expertise in the North American (FDA & Canada) cosmetic, OTC, and natural products industr, capable of independently preparing complex investigation reports, risk assessments, and change control documentation supporting laboratory development through to commercial batch production.
Investigations, Root Cause Analysis & CAPA
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.
R&D Impact & Risk Assessments
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.
Raw Material Assessments
Develop and maintain Raw Material Assessments supporting cosmetic, OTC, and natural products.
Support raw material change evaluations and supplier‑related documentation as required.
Change Control & Technical Transfer
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.
Technical Documentation & SOPs
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.
Cross-Functional Collaboration
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.
Other Duties
Perform other duties as assigned by the Director Technical Services in support of departmental and organizational goals.
JOB REQUIREMENTS
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.
Apollo Health & Beauty Care Ltd. will ensure accommodations are available in consultation with candidates during all stages of the recruitment process. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Duties outlined in this job description may not be all-inclusive, and can be modified at any time if requested by management. Apollo is committed to providing accommodations for people with disabilities in all parts of the hiring process. Apollo will work with applicants to meet accommodation needs that are made known in advance.
We thank all applicants for their interest however only those meeting the minimum qualifications will be interviewed.
Vacancy Status:
This posting represents an
existing vacancy, and we are actively recruiting to fill this position.
Job Criteria
Seniority level:
Mid-Senior level
Employment type:
Full-time
Job function:
Marketing, Public Relations, and Writing/Editing
Industries:
Manufacturing
#J-18808-Ljbffr
Vacancy posted 1 hour ago
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