Technical Writer – SOPs, GDEs

🕒 October 21

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔏 Technical Writer

🚫👨‍🎓 No degree required

👻 Ghost score 12%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Validation & Engineering Group, Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1997

💼 Consulting

🏥 Healthcare

🍽️ Food & Beverage

Consulting • Healthcare • Food & Beverage

Validation & Engineering Group, Inc. is a leading service provider in the biotechnology, food safety and quality, medical devices, and pharmaceutical industries. The company focuses on ensuring quality, compliance, and efficiency across the life sciences industry, offering services such as commissioning & qualification, computer system validation, process and equipment validation, automated process control, and quality systems management. Established in 1997, Validation & Engineering Group operates in Puerto Rico and the USA, adhering to both Federal and European regulatory standards. The company is committed to innovation, trust, and excellence, supporting the industry's growth through expertise, training, and sustainable business practices.

📋 Description

• Draft, revise, and format SOPs and GDE documentation covering engineering systems, equipment, and manufacturing support processes • Translate technical requirements, engineering standards, and subject matter expert input into clear, accurate documents • Ensure consistency with applicable global engineering requirements, site procedures, and GMP standards • Collaborate with Engineering, Manufacturing, Validation, and Quality to resolve comments and complete document reviews • Manage document revisions and approval workflows through the electronic document management system

🎯 Requirements

• Bachelor’s degree in Engineering, Science, Technical Writing, or a related field preferred • At least 2 years of technical writing experience in pharmaceutical or biotechnology operations • Experience with SOPs, engineering documentation, and GMP requirements • Strong English writing skills • Organizational skills and attention to detail

🏖️ Benefits

• Equal opportunity employment • Supportive, purpose-driven team environment • Opportunity to contribute to healthcare and technology • Empowerment to do your best work

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