QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

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The Technical Writer will be responsible for authoring, reviewing, and updating high-quality technical documentation for manufacturing and warehouse processes at the BD El Paso, TX facility. This role focuses specifically on operations involving controlled substances, ensuring all documents strictly adhere to GMP regulations and internal quality standards. The ideal candidate must possess exceptional bilingual communication skills (English and Spanish) to translate effectively and adapt complex technical procedures.

Responsibilities

Technical Writing & Procedure Development

• Document authoring: Write, revise, and format Standard Operating Procedures (SOPs), batch records, work instructions, and training materials for manufacturing and warehouse operations.
• Process review: Review existing technical documentation to identify gaps, streamline workflows, and ensure alignment with actual shop-floor practices for controlled products.
• Cross-functional collaboration: Partner with production, logistics, operations, and quality assurance teams to capture accurate and precise technical information.
• Bilingual translation: Translate and adapt technical procedures between English and Spanish, maintaining absolute clarity, consistency, and regulatory intent in both languages.
• Document control: Coordinate with the Quality Management team to route documents through the lifecycle management system for review, approval, and official issuance.

Requirements

Education

• Degree: Bachelor’s degree required (preferably in Communications, Technical Writing, Engineering, Life Sciences, or a related field).

Experience

• Industry experience: Minimum of 2–4 years of experience working as a Technical Writer in a GMP-regulated environment (Medical Device, Pharmaceutical, or Biotech).
• Controlled products: Proven experience designing, reviewing, or managing documentation related to controlled substances or highly regulated chemical/biological components.
• Document management: Familiarity with Electronic Document Management Systems (EDMS) and strict version control protocols.

Skills & Competencies

• Language: 100% Bilingual (English/Spanish). Must possess outstanding written and verbal communication skills in both languages, with the ability to draft professional technical text.
• Regulatory knowledge: Solid understanding of GMP principles, compliance documentation standards, and basic safety protocols for controlled substance handling.
• Attention to detail: Exceptional ability to transform complex technical data and operational workflows into clear, concise, and structured instructions for end-users.

All your information will be kept confidential according to EEO guidelines.