R&d Technical Writing Associate I
2 weeks ago
**Work mode**:Hybrid**Onsite Location(s)**:Mississauga, ON, CA**Additional Locations**: Canada-ON-Mississauga; Canada-ON-Toronto**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance**
- At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing - whatever your ambitions.**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.**_Please note that this is a 12-month contract position_**
**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
**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)
**_Learn more about our Transseptal Access Devices_**
- Click this link to explore the groundbreaking technology behind our transseptal access devices at Boston Scientific_**_: _**_Transseptal access devices_**
**Requisition ID**:592408- **Job Segment**:Technical Writer, R&D, R&D Engineer, Document Control, Developer, Technology, Research, Engineering, Administrative
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