- Job Description : Technical Writer
- Position Overview :
- We are looking for a detail-oriented Technical Writer to join our team. This role involves creating, editing, and approving technical documents to ensure clarity and compliance within our organization.
The ideal candidate will have experience in a regulated environment and a strong ability to communicate complex information effectively.
Key Responsibilities :
Develop and maintain high-quality technical documents, including manuals, SOPs, and training materials.
Collaborate with subject matter experts to gather information and ensure accuracy in documentation.
Edit and review documents for clarity, grammar, and compliance with internal and regulatory standards.
Approve documents through established workflows and manage version control.
Ensure all technical writing aligns with FDA GMP regulations and industry standards.
Participate in document audits and revisions as needed.
Assist in training staff on documentation processes and standards.
- Qualifications :
- Education :
High School Diploma or higher.
Experience :
2+ years of technical writing experience.
Experience in a regulated industry with FDA GMP knowledge is preferred.
Must-Have Skills :
Technical Writing Expertise : Proven experience in creating, editing, and approving technical documents.
Attention to Detail : Strong focus on accuracy and quality in all written materials.
Effective Communication : Ability to convey complex information clearly to diverse audiences.
Collaboration Skills : Experience working with cross-functional teams to gather information and feedback.
Organizational Skills : Ability to manage multiple projects and meet deadlines consistently.
Nice-to-Have Skills :
Experience with 503B compounding regulations and documentation.
Ideal Characteristics :
Self-motivated and able to work independently.
Adaptable to changing priorities and fast-paced environments.
Committed to continuous improvement and professional development.