Technical Writer (SOP Development, Manufacturing Operations)
Role: Create, revise, and manage SOPs and technical documents for biopharma manufacturing operations.
Responsibilities
* Develop and maintain SOPs that comply with GMP, GDP, and regulatory standards.
* Collaborate with SMEs to gather accurate process information.
* Standardize documentation using templates and style guides.
* Support training sessions and create training materials based on SOPs.
* Manage controlled documents using document management systems.
Qualifications
* Bachelor’s degree in Technical Writing, Life Sciences, or related field.
* 3-5 years of experience in biopharma/pharma manufacturing documentation.
Skills
* Strong writing, editing, and proofreading skills.
* Knowledge of GMP, FDA regulations, and biopharma manufacturing processes.
* Proficiency in document management tools (e.g., Veeva).
Location: Limerick, County Limerick, Ireland.
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