Quality Associate I - Filling (1st shift)
Simtra BioPharma Solutions(3 days ago)
About this role
The Quality Associate I supports the quality assurance operations in a pharmaceutical manufacturing environment. They ensure compliance with regulatory standards, review manufacturing records, and assist with audits and process improvements.
Required Skills
- GMP
- Quality Assurance
- Regulatory Compliance
- Record Review
- SOP
- Audit Support
- Aseptic Processing
- CAPA
- cGMP
- Risk Assessment
About Simtra BioPharma Solutions
simtra.comSimtra 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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