Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance
Job Summary
Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance.
The MQ TS Downstream Associate is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards.
By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.
Matching Summary
Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance.
Skills & Requirements
Must-have
cGMP compliance monitoring
Batch record review and release
Terminal sterilization process oversight
Visual inspection and packaging quality control
Equipment audit trail review
Acceptable Quality Level sampling
Nice-to-have
Troubleshooting manufacturing issues
Process and procedure simplification
Effective team collaboration
Written and oral communication skills
Key Requirements
M. Pharma or MSc degree
More than 1 year experience in pharmaceutical QA or production
Experience in pharmaceutical industry quality systems
Sound knowledge of current Good Manufacturing Practices (cGMP)