Perform and oversee analytical testing of raw materials, intermediates, finished products, stability samples, process aids, and packaging materials using techniques including HPLC, UPLC, GC, capillary electrophoresis (CE), particle counting, and other analytical methods.
Lead analytical method transfers, verifications, qualifications, and validations for new products and customer projects.
Support qualification of laboratory equipment, analytical instruments, computerized laboratory systems, and new laboratory capabilities.
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Perform and oversee analytical testing of raw materials, intermediates, finished products, stability samples, process aids, and packaging materials using techniques including HPLC, UPLC, GC, capillary electrophoresis (CE), particle counting, and other analytical methods.
Lead analytical method transfers, verifications, qualifications, and validations for new products and customer projects.
Support qualification of laboratory equipment, analytical instruments, computerized laboratory systems, and new laboratory capabilities.
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Advanced degree plus 3 years of experience, or Bachelor's degree plus 5 years of experience in software testing, including both manual and automated testing
Strong knowledge and expertise in embedded system/hardware
Preferred Fields of Study: Computer Science, Engineering, Electronics, or related field
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Assemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.
Follow standard work instructions and interpret technical drawings to ensure consistent product quality.
Maintain strict adherence to ISO 13485:2016, ISO 22301:2019, and current Good Manufacturing Practices (cGMP) documentation standards to ensure regulatory compliance and quality assurance.
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Assemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.
Follow standard work instructions and interpret technical drawings to ensure consistent product quality.
Maintain strict adherence to ISO 13485:2016, ISO 22301:2019, and current Good Manufacturing Practices (cGMP) documentation standards to ensure regulatory compliance and quality assurance.
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