Hybrid Technical Writer II - Regulated Docs & Compliance

Baylis Medical Technologies; Mississauga; Hybrid; CAD 65,000 - 90,000; Full time

Benefits offered by this job

Shuttle service

Hybrid work model

Volunteer day

Training programs

Tuition reimbursement

Health spending account

Employee clubs

Job summary

Baylis Medical Technologies in Mississauga, Canada, seeks a Technical Writer II to translate complex engineering and regulatory information into clear SOPs, work instructions, design history records, and validation protocols. You work with engineers, quality, and regulatory teams to shape documentation processes and support continuous improvement.

You will develop templates, manage document life cycles in the eQMS, and collaborate with cross-functional teams to ensure timely approvals and

Qualifications

• Technical degree or technical writing certification with 2 years’ experience in technical writing or equivalent.
• Competence in creating and editing technical documentation in a regulated environment.
• High accuracy and attention to detail in document creation and review.

Responsibilities

• Translate technical information into SOPs, work instructions, and quality documents.
• Collaborate with SMEs and engineering to gather information from drawings and reports.
• Route documents through the eQMS and monitor review cycles and approvals.
• Support continuous improvement of documentation templates, workflows, and procedures.

Skills

Technical writing

Regulatory documentation

Attention to detail

Team collaboration

Deadline management

English communication

Education

Technical degree

Technical writing certification

Tools

MS Office

eQMS

Job description

Baylis Medical Technologies in Mississauga, Canada, seeks a Technical Writer II to translate complex engineering and regulatory information into clear SOPs, work instructions, design history records, and validation protocols. You work with engineers, quality, and regulatory teams to shape documentation processes and support continuous improvement.

You will develop templates, manage document life cycles in the eQMS, and collaborate with cross-functional teams to ensure timely approvals and