Technical Writer SOP Development Manufacturing Site
Technical Writer SOP Development Manufacturing Site
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1-3years
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
This is a remote position.
Key Responsibilities:
Develop revise and maintain SOPs to support site readiness and technical operations.
Collaborate with crossfunctional teams to gather technical information and ensure accurate documentation.
Apply knowledge of CGMPs drug/device development and manufacturing processes to technical writing tasks.
Support process development scaleup qualification and technology transfer initiatives.
Assist in the design specification selection implementation and startup of manufacturing facilities utilities equipment and systems.
Participate in troubleshooting root cause analysis and continuous improvement efforts for processes and equipment.
Contribute to project estimating capital requests vendor selection and project budgeting.
Assist in creating and managing project timelines and deliverables.
Requirements
Bachelors Degree in a sciencerelated field such as Biomedical Engineering Mechanical Engineering or Chemical Engineering.
Demonstrated experience in generating SOPs for manufacturing or technical operations.
Indepth knowledge of technical writing practices CGMP standards and drug/device development processes.
Familiarity with project management concepts and tools.
Strong proficiency in MS Office products including Outlook Excel PowerPoint and Word.
Excellent written and verbal communication skills with attention to detail.
Preferred Skills:
Experience supporting process development and technology transfer in a manufacturing setting.
Ability to troubleshoot and provide innovative solutions for process improvement.
Understanding of project lifecycle from concept to implementation.
Benefits
- Remote work
- Competitive rates
Bachelor's Degree in a science-related field such as Biomedical Engineering, Mechanical Engineering, or Chemical Engineering. Demonstrated experience in generating SOPs for manufacturing or technical operations. In-depth knowledge of technical writing practices, CGMP standards, and drug/device development processes. Familiarity with project management concepts and tools. Strong proficiency in MS Office products, including Outlook, Excel, PowerPoint, and Word. Excellent written and verbal communication skills with attention to detail. Preferred Skills: Experience supporting process development and technology transfer in a manufacturing setting. Ability to troubleshoot and provide innovative solutions for process improvement. Understanding of project lifecycle, from concept to implementation.
Employment Type
Full Time
