BioPharma Technical Writer — SOPs, Validation & Documentation

Eurofins USA Clinical Trial Solutions; Lenexa (KS); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, dental & vision benefits

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA Clinical Trial Solutions is seeking a BioPharma Technical Writer to develop and maintain controlled documentation that supports validation and laboratory operations. You will ensure SOPs, forms, and protocols are accurate, clear, and compliant, working with cross‑functional SMEs to ensure quality and continuous improvement.

The role includes contributing at two levels (I and II) with increasing responsibility for templates, templates creation, and process improvements, in a

Qualifications

• Bachelor’s degree in medical laboratory sciences, biology, chemistry, or another relevant scientific discipline required.
• Additional education or professional experience in technical, scientific, medical, or regulatory writing preferred.

Responsibilities

• Write and edit forms, protocols, reports, and procedures from templates under supervision.
• Analyze documents to maintain continuity of style and content.
• Update and revise technical documents as instructed.
• Collaborate with Scientists, Regulatory Affairs, and R&D.
• BioPharma Technical Writer II: create/modify templates and participate in process improvements.

Skills

Technical writing excellence

Grammar and editing

Documentation review

Organization

Attention to detail

Cross-functional collaboration

Independent work

Education

Bachelor’s degree in a relevant scientific field

Job description

Eurofins USA Clinical Trial Solutions is seeking a BioPharma Technical Writer to develop and maintain controlled documentation that supports validation and laboratory operations. You will ensure SOPs, forms, and protocols are accurate, clear, and compliant, working with cross‑functional SMEs to ensure quality and continuous improvement.

The role includes contributing at two levels (I and II) with increasing responsibility for templates, templates creation, and process improvements, in a