Quality Associate I - Filling (3rd Shift)
Simtra BioPharma Solutions(12 days ago)
About this role
A Quality Associate I at Simtra BioPharma Solutions supports the manufacturing process by monitoring quality compliance and participating in audits and continuous improvement initiatives. The role emphasizes quality assurance, regulatory adherence, and teamwork within a manufacturing environment focused on sterile injectable products.
Required Skills
- cGMP
- Quality Assurance
- Regulatory Compliance
- Audit
- SOP
Qualifications
- Bachelor’s degree in Science, or Associate’s degree with experience, or no degree with experience
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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