Thermo Fisher Scientific·14 days ago
14 days ago
Quality Specialist III (1 Day Shift & 2 Night Shift Positions)
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What you'll do
- Ensure regulatory compliance and continuous improvement in a dynamic pharmaceutical environment
- Collaborate with cross-functional teams
- Conduct audits
- Drive quality excellence
What they're looking for
- strong experience in GMP
- ISO standards
- quality systems
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Embrace the opportunity to become a Quality Specialist III and play a key role in ensuring regulatory compliance and continuous improvement in a dynamic pharmaceutical environment. Collaborate with cross-functional teams, conduct audits, and drive quality excellence. If you have strong experience in GMP, ISO standards, and quality systems, this is your opportunity to make an impact.
Skills
- gmp compliance
- quality management systems
- capa processes
- quality systems software
- corrective action implementation
- quality metrics reporting
- investigation techniques
- deviation management
- sop authoring
- internal audits
- external audits
- gxp regulations
- regulatory inspections
- trackwise
- data trending
- continuous improvement
- document control systems
- root cause analysis
- iso 9001
- change control
Company
Thermo Fisher Scientific
Greenville, United States of America
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