This individual will primarily support updating documents to meet a corporate dateline for the site to align its SOPs to corporate policies. Additionally, this position will help update documents related to CAPAs while freeing up bandwidth from QC Analysts to stay in the lab testing products.
Coordinate and execute document revisions within the Quality organization (QA/QC).
Update local documents to align with corporate policies.
Update documents as required per CAPAs, Change Control, etc.
Update document from an old template to the new template.
Work with different groups to optimize documents as required.
Support other activities as assigned.
Associates degree in a STEM discipline and >6 years related experience
Bachelor's degree in a STEM discipline and 3-6 years related experience
Masters degree in a STEM discipline and 1-3 years related experience
Advanced knowledge of Word, Excel, PowerPoint, and other and applies technical knowledge to assist the site with Microsoft troubleshooting.
Has basic knowledge of the principles, theories, and concepts applicable to a wide range of work in a discipline.
Ability to peer-review processes to ensure procedures are well organized with clear instruction.
Ability to understand and write SOPs and batch production records independently.
Excellent written communications skills with internal and external customers; Scientific writing skills.