Technical Writer - Life Sciences & Med Devices

Oxford Global Resources; Belfast City District; On-site; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Pension contributions

Health insurance

Paid holidays

Job summary

Oxford Global Resources in Belfast is seeking a Technical Writer to develop, standardize, and maintain clear, compliant documentation including operating procedures, work instructions, and forms.

The role involves collaborating with SMEs, process owners, and cross-functional teams to translate complex processes into user-friendly documentation while ensuring alignment with QMS requirements and regulatory standards.

Qualifications

• Bachelor's degree in Engineering, Technical Communication, English, Life Sciences, or related field or equivalent experience.
• 3+ years of experience in technical writing, preferably in regulated industries (medical devices, pharmaceuticals, manufacturing).
• Strong knowledge of operating procedures, work instructions, and controlled forms.
• Familiarity with Quality Management Systems (ISO 9001, ISO 13485) and regulatory requirements preferred.

Responsibilities

• Develop, write, edit, and maintain SOPs, work instructions, and forms in line with policies and regulatory requirements.
• Partner with SMEs and process owners to gather information and ensure accuracy of technical content.
• Standardize documentation format and ensure consistency across departments.

Skills

Technical writing

Regulated industries

Quality standards

MS Office

SharePoint

Documentation management

Collaboration

Analytical thinking

Education

Bachelor's degree

Tools

SharePoint

MasterControl

Microsoft Office

Job description

Oxford Global Resources in Belfast is seeking a Technical Writer to develop, standardize, and maintain clear, compliant documentation including operating procedures, work instructions, and forms.

The role involves collaborating with SMEs, process owners, and cross-functional teams to translate complex processes into user-friendly documentation while ensuring alignment with QMS requirements and regulatory standards.