Technical Writer

2 weeks ago


Mississauga, Canada SGS Full time

Company Description

WE ARE SGS - THE WORLD’S LEADING TESTING, INSPECTION AND CERTIFICATION COMPANY. WE ARE RECOGNIZED AS THE GLOBAL BENCHMARK FOR QUALITY AND INTEGRITY. OUR 96,000 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 other technical documents when necessary.
- Contract 12 - 18 months.
- Responsible for supporting the Operations team to prepare the documentation as required by clients, including follow up of change controls, maintaining the templates for laboratory documents
- Responsible for periodic review of the compendia changes and providing evaluation as it impacts the Biopharmaceutical Services department.
- Works with laboratory personnel to write or review protocols and/or reports for method development, feasibility, transfer, verification and validation projects.
- Work with laboratory personnel to write or review client methods for routine sample analysis as needed.
- Ensure timely review of compendia updates, such as USP, EP, JP.
- Document and communicate the compendia changes to the impacted groups.
- Maintain templates for various lab documents.
- Ensure documentation is controlled and follows SGS procedures.
- Participate in departmental or company-wide projects to improve the internal efficiency and overall quality of work performed by the laboratory.
- Perform other assigned duties as requested.

**Qualifications**:

- Bachelor's or master's degree in Biological Chemistry or a related science degree and two or more years of related pharmaceutical experience
- Must be able to communicate clearly in English and have solid communication skills including grammer and composition.
- have excellent interpersonal skills.
- Ability to work well with others and independently.
- Proven time management skills and a strong attention to detail.
- Demonstrate understanding of cGMP regulations.
- Proficient in using various types of computer software (Word, Excel, etc.)
- Ensure full compliance with the company's Health & Safety Code of Integrity and Professional Conduct Policies.

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