Job Description

Summary:
We are looking to support a partnered firm in the USA to develop and execute a project in Glaxo Smith Kline (GSK) - Marietta, PA-USA facility in the Validations Master Plan creation for three (3) facilities and all equipment related Validation Processes including Qualification and Validations. This role is classified as Technical position.



Main Responsibilities:

1. Responsible for writing, reviewing and revising both written and visual technical communications related to the development of Validation Master Plan for a Pharmaceutical industry and all associated documents.
2. Reviewing and revising technical communications.
3. Learning and conforming to relevant style guides and standards.
4. Conducting research on products and technical communication best practices.
5. Collaborating with developers, engineers and other teams to understand technical / specialized terms/areas.
6. Delegating tasks to other technical writers.
7. Overseeing the work of other writers to ensure they follow style and quality standards.
8. Collecting and applying user feedback.

Requirements:

• Bachelor's degree in Administration or Science
• 5-7 years of experience in technical writing for regulated industries such Pharmaceutical, Biotechnology or Medical Devices
• Fully bilingual: English and Spanish (written and verbal)
• Great technical writing skills and experience in English
• Leadership, interaction with multidisciplinary teams experience

Work Methodology:

• 100% on-site job in Marietta, Pennsylvania, USA
• Full time project with overtime
• Professional services agreement
• Expected project starting date: Sept. 23, 2024
• All Inclusive rate which covers hours worked + allocation expenses (lodging, meals, transportation, etc.)
• 5 months of the 1 st contract with potential extension

Job Tags

Full time, Contract work,

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