of manufacturing/quality systems, including deviations, equipment qualification, process validation, procedures, training, and new...Job Description: Under general supervision, the Manufacturing/Process Engineer provides technical support for process...
, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process... and/or process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise...
. Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise.... Process Validation 1. Assist with generation of process validation protocols and reports. 2. Assist with the execution...
. Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
shift (If require) mainly first shift Minimum 2 years in experience in Process Validation and / Computer System...Process Engineer I requires: Availability to work extended shifts (8- 12 hours per shift) Availability to work...
of manufacturing such as non-conformances, process validation, procedures, training, and new product introductions. Apply process... with generation of process validation protocols and reports. Participate in the NPI process to assess requirements for documentation...
, and execution of validation protocols, ensuring accurate process documentation and deviation management. Apply advanced validation... impact. Work closely with Manufacturing, Process Development, Utilities, Labs, and Quality Assurance to develop requirements...
of manufacturing such as non-conformances, process validation, procedures, training, and new product introductions. Apply process... with generation of process validation protocols and reports. Participate in the NPI process to assess requirements for documentation...
, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing... requirements and recommendations for process and/or system modifications. Support the execution of manufacturing/quality systems...
, manufacturing, maintenance, process development, utilities, facilities, quality assurance, and/or validation departments. Work... AM Experience in: Equipment and/or process troubleshooting in a regulated environment. Pharmaceutical/biotech processes and GMP...
. Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation... of manufacturing/quality systems such as deviations, equipment qualification and/or process validation, procedures, training, and new...
, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations... for process and/or system modifications. * Support the execution of manufacturing/quality systems such as deviations, equipment...
. Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation... of manufacturing/quality systems such as deviations, equipment qualification and/or process validation, procedures, training, and new...
. - Approve process validation protocols and reports for manufacturing processes. - Request Quality on incident triage team..., QAL, validation and process development. - Demonstrate ability to interact with regulatory agencies. - Strong word...
, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations... for process and/or system modifications. * Support the execution of manufacturing/quality systems such as deviations, equipment...
of manufacturing/quality systems including deviations, equipment qualification, process validation, procedures, training, and new..., and validation departments to develop requirements and recommendations for process and/or system modifications. Support execution...
experience in Medical Device industry Root Cause Analysis Process Validation (IQ/PD/OQ/PQ) Technical Writing 12 Hour Night...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
What are the top 3 things you are looking for in a candidates experience: 1. Root Cause Analysis 2. Process... Validation (IQ/PD/OQ/PQ) 3. Technical Writing Education Required: BS in Engineering. Years’ Experience Required: 1-3 Years...
experience in Medical Device industry Root Cause Analysis Process Validation (IQ/PD/OQ/PQ) Technical Writing 12 Hour Night...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...