Technical Writer R&D - 18-month Maternity Leave at SGS

Markham, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

20 Jan, 26

Salary

0.0

Posted On

23 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Technical Writing, Pharmaceuticals, Project Management, cGMP, Laboratory Procedures, Documentation, Change Control, Method Development, Feasibility Studies, Validation, Report Writing, Compendia Updates, Collaboration, Resource Management, SOPs, Analytical Operations

Industry

Professional Services

Description

Company Description We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. 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 departments. Qualifications • Bachelors Degree • Masters in Science • 3 to 5 years experience in a laboratory setting with Min 2 years of Pharmceutical Technical Writing • Demonstrated work with cGMP • Proficient with lab software Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression and Indigenous status, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities, or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. Accommodations are available on request for qualified candidates during each stage of the recruitment process. Please note that candidates applying for Canadian job openings should be authorized to work in Canada.

Responsibilities

The Technical Writer is responsible for writing methods, protocols, reports, and SOPs, while managing medium to larger projects in collaboration with clients and internal resources. They will support R&D scientists in preparing documentation and ensure timely reviews of compendia updates.