R&D Technical Writing Associate I
at Boston Scientific Corporation
Mississauga, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Communication Skills,Technical Writing | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
REQUIRED QUALIFICATIONS
- Actively working towards or completed a degree in Engineering, Science or Technical Writing
- Proficient with Microsoft Office suite
- Ability to work independently and in a multidisciplinary team environment
PREFERRED QUALIFICATIONS
- Demonstrated competence as a Technical Writer or Engineer through previous co-ops, course projects or work experience
- Experience working in regulated manufacturing industry
- Experience working within document control or electronic quality management systems (eQMS)
- Self-starter with the ability to quickly learn new processes
- Strong attention to detail
- Ability to reliably meet deadlines and project objectives
- Excellent analytical and communication skills (both written and oral)
Responsibilities:
ABOUT THE ROLE
The R&D Technical Writing Associate will join the Access Solutions site to contribute to our ongoing product labelling update project. This role will work in a team of dedicated labelling experts with the project leaders to ensure labelling documents (on-device labels and instructions for use) are authored, reviewed and approved while following internal procedures and international regulatory requirements.
YOUR RESPONSIBILITIES WILL INCLUDE:
- Conduct visual gap assessments to identify and document all changes made to previous revisions of product labels and user instructions
- Contribute to change assessment documentation
- Schedule and coordinate stakeholder reviews of completed documentation
- Collaborate with SMEs to gather technical information as required
- Update existing labelling documentation using authoring software as needed
- Maintain internal project tracker(s) to capture status of deliverables and overall project health
- Navigate and/or create electronic records within quality management system
- Contribute to team meeting discussions regarding project status, successes and roadblocks
- Adhere to and promote the adherence to all Corporate, Quality and Health and Safety policies and procedures
- Other duties as required
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
IT Software - Other
Software Engineering
Graduate
Technical Writing, Engineering
Proficient
1
Mississauga, ON, Canada