Job Description

Job ID: 21-12907
Skills:
-Ability to write technical documents, and tenacious attention to detail and consistency, especially with respect to style, format, and layout for visual design simplicity is a must.

-Previous experience with documents in a regulatory environment is preferred and knowledge or experience in the biotech or pharmaceutical manufacturing industry is beneficial.

-Proficiency in a broad range of technical skills, including expert-level use of Google Software, MS Excel, Word, PowerPoint, Visio is required and knowledge of document management systems (e.g. Condor and Veeva), quality systems (Veeva) and document collaboration systems (e.g. SmartSheets) are beneficial.

-An aptitude for teamwork and the ability to collaborate effectively with leaders, engineers and subject matter experts is needed.

-Strong organizational and time-management skills; the ability to deliver under pressure; and the ability to work flexibly to support changing assignments and priorities in an independent and reliable manner.

-Exceptional written and oral communication skills.

-Proven ability to create strong working relationships with respect to cultural diversity and working styles.

-Demonstrated ability to organize and execute on a variety of assignments and action plans.

-Ability to translate complex concepts into written and visual documentation.

Education:

Minimum BA or BS (or equivalent) in English, biology, chemistry, pharmacy, or a related field, or previous experience working in the pharmaceutical field

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