Quality Documentation Specialist

Simtra BioPharma Solutions(10 days ago)

Indiana, Bloomington, IN, United StatesOnsiteFull TimeMedior$0 - $0Documentation/Quality Assurance

About this role

Simtra BioPharma Solutions is a contract development and manufacturing organization specializing in sterile injectable products, biologics, and small molecules. The company emphasizes quality, regulatory compliance, and supporting life-changing medicines, with facilities in the US and Germany.

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Required Skills

Veeva
ERP
Documentation
Quality Control
Batch Records
Regulatory Compliance
Process Management
GMP
Continuous Improvement
Teamwork

About Simtra BioPharma Solutions

simtra.com

Simtra BioPharma Solutions is a contract development and manufacturing organization (CDMO) focused on sterile injectable products. They offer end-to-end services — from formulation and analytical development through aseptic fill/finish, packaging, quality and regulatory support — to advance programs from clinical stages to commercial supply. Simtra emphasizes flexible product delivery options and a compliance-driven approach to meet biopharma partners’ timelines and manufacturing requirements.

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