Manufacturing Technical Writer - SOPs & Validation (Onsite)

Pride Health

San Diego (CA)

On-site

USD 55,000 - 61,000

Full time

14 days+

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Benefits offered by this job

Healthcare coverage
401(k) retirement savings
Life & disability insurance
Employee discounts

Job summary

Pride Global, supporting a leading medical device manufacturer, seeks a Technical Writer - Manufacturing Documentation in San Diego, CA. This onsite role concentrates on creating, editing, and maintaining manufacturing documentation, including work instructions, SOPs, and equipment documentation to support production and regulatory compliance.

You'll collaborate with manufacturing engineers and SMEs to capture experimental design, validation results, and engineering activities, translating

Qualifications

  • Bachelor's degree in engineering or related technical field.
  • Minimum 3-4 years of technical writing in manufacturing/engineering.
  • Experience documenting manufacturing equipment, processes and procedures.
  • Ability to capture experimental design and validation results in documentation.

Responsibilities

  • Create, edit, and maintain manufacturing documentation including SOPs and work instructions.
  • Draft and release Manufacturing Process Instructions for production.
  • Prepare Equipment Documentation Packets (URS, IQ, OQ, PQ).
  • Capture experimental designs and validation results into clear documentation.
  • Collaborate with engineers and production teams to ensure accuracy.

Skills

Technical writing
Manufacturing documentation
SOPs
Work instructions

Education

Bachelor's degree in Engineering
Engineering-related field

Tools

Document control systems
Quality management system

Job description

Pride Global, supporting a leading medical device manufacturer, seeks a Technical Writer - Manufacturing Documentation in San Diego, CA. This onsite role concentrates on creating, editing, and maintaining manufacturing documentation, including work instructions, SOPs, and equipment documentation to support production and regulatory compliance.

You'll collaborate with manufacturing engineers and SMEs to capture experimental design, validation results, and engineering activities, translating

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