R&D Technical Writing Associate I

at  Boston Scientific Corporation

Mississauga, ON, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Jan, 2025Not Specified19 Oct, 2024N/ACommunication Skills,Technical WritingNoNo
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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