Bilingual GMP Technical Writer: Controlled Substances

QRC Group

Caguas (PR)

Hybrid

USD 50,000 - 80,000

Full time

13 days ago

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Job summary

Zohorecruit is seeking a Technical Writer to author, review, and update GMP-compliant documentation for manufacturing and warehouse processes at the BD El Paso, TX facility. The role focuses on controlled substances and requires exceptional bilingual English/Spanish communication to translate and adapt complex procedures.

You will produce SOPs, batch records, work instructions, and training materials, collaborating across production, logistics, operations, and quality teams while ensuring strict

Qualifications

  • Bachelor’s degree in a relevant field (Communications, Technical Writing, Engineering, Life Sciences).
  • 2–4 years in a GMP-regulated environment (Medical Device, Pharmaceutical, or Biotech).
  • Experience with controlled substances documentation and regulatory standards.
  • Proficiency in bilingual technical writing English/Spanish.

Responsibilities

  • Author, review, and update SOPs, batch records, work instructions, and training materials for manufacturing and warehouse operations.
  • Review existing documentation to identify gaps and improve alignment with shop-floor practices for controlled products.
  • Collaborate with production, logistics, operations, and QA to capture accurate technical information.
  • Translate and adapt procedures between English and Spanish while preserving regulatory intent.

Skills

Bilingual English/Spanish
Document authoring
Process review
Cross-functional collaboration
Document control

Education

Bachelor’s degree

Tools

EDMS (Electronic Document Management System)

Job description

Zohorecruit is seeking a Technical Writer to author, review, and update GMP-compliant documentation for manufacturing and warehouse processes at the BD El Paso, TX facility. The role focuses on controlled substances and requires exceptional bilingual English/Spanish communication to translate and adapt complex procedures.

You will produce SOPs, batch records, work instructions, and training materials, collaborating across production, logistics, operations, and quality teams while ensuring strict

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