Technical Writer – Medical Devices & Regulatory Docs

Fisher Paykel Healthcare; Auckland; On-site; NZD 65,000 - 90,000; Full time

Benefits offered by this job

Employee share purchase scheme

Bi-annual Profit share

Life, Critical illness and Income/Dis.

Discounted Health Insurance

Active social clubs & community groups

In-house training programs

Purchasing privileges for products

Banking and Insurance discounts

Free Parking

Beautiful campus with green spaces

Annual Salary Review

High rates of internal promotion

Access to state-of-the-art facilities

Job summary

Fisher & Paykel Healthcare is seeking a Technical Writer to join our team for an 18-month fixed-term contract in Auckland. You will create, maintain and improve product documentation for a regulated medical device portfolio and translate complex technical information into clear, compliant documents.

Collaborating with subject matter experts across development, clinical, regulatory and post-market activities, you’ll ensure accuracy, traceability and adherence to quality systems while supporting

Qualifications

• Experience creating complex technical documentation
• Strong attention to detail and commitment to accuracy
• Ability to manage multiple projects and deadlines simultaneously
• Proficiency with Microsoft Office and electronic document management systems
• Familiarity with medical device regulation and quality management systems

Responsibilities

• Create, maintain and improve product documentation
• Translate technical information into clear, concise, compliant documentation
• Collaborate with subject matter experts across product development, regulatory and post-market
• Ensure documentation meets regulatory requirements and quality systems

Skills

Technical writing

Documentation drafting

Attention to detail

Project management

Microsoft Office

Education

Relevant tertiary qualification in science, engineering or related field

Tools

Electronic document management systems

Microsoft Office

Job description

Fisher & Paykel Healthcare is seeking a Technical Writer to join our team for an 18-month fixed-term contract in Auckland. You will create, maintain and improve product documentation for a regulated medical device portfolio and translate complex technical information into clear, compliant documents.

Collaborating with subject matter experts across development, clinical, regulatory and post-market activities, you’ll ensure accuracy, traceability and adherence to quality systems while supporting