Regulated Medical Device Technical Writer

Intellectt Inc; Indiana (PA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading regulated manufacturing firm in Indiana is seeking a detail-oriented Technical Writer to support the creation and management of controlled documentation within a regulated environment. The ideal candidate will have over 3 years of experience in technical writing and must be proficient in electronic document management systems like Veeva Vault. Key responsibilities include developing SOPs, collaborating with cross-functional teams, and ensuring compliance with regulatory standards.

Qualifications

• 3+ years of technical writing experience in a regulated environment.
• Hands-on experience with electronic document management systems (eDMS).
• Experience developing controlled documentation like SOPs and training materials.

Responsibilities

• Develop, revise, and format Standard Operating Procedures (SOPs).
• Collaborate with cross-functional teams to gather technical content.
• Ensure documentation complies with regulatory requirements.

Skills

Attention to detail

Excellent written communication

Excellent verbal communication

Experience with electronic document management systems

Education

Bachelor’s degree in Engineering, Life Sciences, Technical Communication, or related field

Tools

Veeva Vault

Job description

A leading regulated manufacturing firm in Indiana is seeking a detail-oriented Technical Writer to support the creation and management of controlled documentation within a regulated environment. The ideal candidate will have over 3 years of experience in technical writing and must be proficient in electronic document management systems like Veeva Vault. Key responsibilities include developing SOPs, collaborating with cross-functional teams, and ensuring compliance with regulatory standards.