Technical Writer, Technical Operations (cGMP)

August Bioservices, LLC; Nashville (TN); On-site; USD 70,000 - 85,000; Full time

Job summary

A leading biotechnology company in Nashville is seeking a Technical Writer for its Technical Operations department. The role focuses on coordinating the creation and revision of essential technical documents such as Batch Records and SOPs. Ideal candidates will have 2+ years of experience in a pharmaceutical environment, proficiency in technical writing, and strong communication skills. This position includes managing multiple projects and collaborating closely with R&D scientists. The company offers a dynamic work environment with growth opportunities.

Qualifications

• 2+ years work experience in a pharmaceutical or life science related field.
• Ability to understand and apply GMP regulations as they relate to pharmaceutical manufacturing.
• Familiarity with cGMP quality systems.

Responsibilities

• Revision/creation of SOP’s, Master Batch Records, and Summary reports.
• Tracking Change Controls, CAPA’s, and collaborating with stakeholders.
• Managing multiple projects and timelines while adhering to standard timelines.

Skills

Technical writing in cGMP or FDA regulated environments

Strong written and verbal communication skills

Managing multiple projects

Proficiency with Microsoft Office Suite

Education

Bachelor's degree in science, technology, or related field

Job description

A leading biotechnology company in Nashville is seeking a Technical Writer for its Technical Operations department. The role focuses on coordinating the creation and revision of essential technical documents such as Batch Records and SOPs. Ideal candidates will have 2+ years of experience in a pharmaceutical environment, proficiency in technical writing, and strong communication skills. This position includes managing multiple projects and collaborating closely with R&D scientists. The company offers a dynamic work environment with growth opportunities.