Technical Writer I, (Pharma Manufacturing Quality) (s494)

Job description
Lenox Executive Search is seeking a Technical Writer I to fill a 12+ month, contractual position with a leading global pharmaceutical company. In this role you will perform technical writing and editing for all types of Pharma Manufacturing and Quality documentation. This is a Hybrid position (Onsite 3-4 days a week) based in Swiftwater, PA.

RESPONSIBILITIES of the Technical Writer I:

• Responsible for designing, developing, and updating required technical documentation
• Responsible for technical writing/editing for all types of documentation produced within a modern software development environment.
• Utilize knowledge of word processing software, strong writing and analytical skills to document software capabilities and functionality.
• Document programming standards and procedures.
• Track and review change control documentation. Assist with the editing of quality documents (SOP’s, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
• Must be able to work quickly with a high degree of accuracy.
• Must possess sound interpersonal and information gathering skills, be able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.
• Review current documents- incorporate comments from Manager
• Navigate through in house computerized systems utilizing current templates
• Notify manager of workflow status and issues.
• Incorporate comments from team members and provide status to manager on review and approval workflow.
• Follow up with team members on comments.

REQUIREMENTS for the Technical Writer I:

• Bachelor’s degree is preferred but not required. Secondary Education diploma a requirement.
• 3-5 years of technical writing (authoring operational procedures and execution records)
• Experience in Pharma strongly preferred
• Well organized, having great communication skills
• Technical writing abilities and good time management.
• Strong root cause analysis skills with experience regarding quality standards.
• Be able to establish working relationships with other support and production areas in order to gather all the necessary information required.
• Must be proficient in Geode+ with a working knowledge of templates, workflows and approval processes.
• Proficient in Microsoft suite, Visio and Adobe.
• Interact well with a diverse group of individuals.
• Self-motivated and willing to be proactive in resolving issues

•. Excellent Verbal and written communication skills.

• Ability to work in a team environment.
• Covid Vaccination is required