
Recruitment • Healthcare • Pharmaceuticals
Hireblox is a staffing agency that specializes in providing high-quality talent for various industries including healthcare, information technology, pharmaceuticals, and insurance. With a focus on understanding the specific workforce needs of their clients, Hireblox is committed to delivering experienced and hardworking professionals to help organizations achieve their goals. Whether for recruitment of full-time employees or contract hires, Hireblox offers expert guidance and tailored services to ensure client satisfaction.
April 8
🇺🇸 United States – Remote
⏳ Contract/Temporary
🟡 Mid-level
đźź Senior
🔏 Technical Writer

Recruitment • Healthcare • Pharmaceuticals
Hireblox is a staffing agency that specializes in providing high-quality talent for various industries including healthcare, information technology, pharmaceuticals, and insurance. With a focus on understanding the specific workforce needs of their clients, Hireblox is committed to delivering experienced and hardworking professionals to help organizations achieve their goals. Whether for recruitment of full-time employees or contract hires, Hireblox offers expert guidance and tailored services to ensure client satisfaction.
• This is a remote position. • Job Title: Technical Writer. • Number of resources: 4. • Location: Onshore (US Eastern Time Hours). • Duration: 6 months with a potential extension of another 6 months. • Responsibility for developing and revising procedures (Procedures, Work Instructions, Job Aides) with input from cross-functional teams, subject matter experts, and the Global Process Owners. • This role requires a deep understanding of GxP practices, particularly in Document Management, and Learning Management systems. • Key Responsibilities: • Create and revise high quality procedures under the guidance of the Global Process owner (GPO). • Incorporate all technical and business process requirements into clear, concise and compliant procedural documents. • Work closely with cross-functional teams to gather information and ensure documentation meets needs. • Utilize technical writing best practices. Collaborate with project team, subject matter experts to gather and validate information. • Ensure that all procedures and documents comply with GxP (Good Practice) standards. • Conduct regular audits to verify compliance and identify areas for improvement. • Develop training materials and user guides to support the implementation of new procedures. • Collaborate with the Learning and Development team to ensure that training content is effective and up-to-date. • Communicate effectively with cross-functional teams, including Quality, Operations, and IT.
• Industry Experience: 3+ years of experience in the Pharma and/or Consumer Health industry. • Strong understanding of regulatory requirements and industry standards. • Previous experience in Document Management systems (e.g., Veeva, Documentum, Tru) to create, store, and manage documents is preferred. • Previous experience with Document Management, GxP Records and Learning Management processes in regulated business is preferred. • Technical Writing Experience: • 3+ years of experience in technical writing, with a focus on procedure development and revision. • Proven ability to write clear, concise, and accurate technical documents. • Strong knowledge of Microsoft Office Suite (Word, Excel, PowerPoint). • Language Proficiency: • High proficiency in English, both written and verbal. • Soft Skills: • Excellent communication and interpersonal skills. • Structured and well-organized. • Strong attention to detail and ability to manage multiple projects simultaneously. • Ability to work independently and as part of a team.
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