Director of QA Jobs in Puerto Rico
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Qa Specialist 35383 Microbiology
Integrated Services For Productivity & Validation, Inc
Knowledge in: Environmental Monitoring Microbial Identification (Micro ID) Critical Utilities (CU) monitoring Sampling monitoring: equipment and techniques Data trending and evaluation Microbiological testing methods and standards for clean rooms and controlled environments Aseptic behavior in manuf...
Qa Investigations Lead
Qrc Group, Llc
QA Investigations Lead to oversee and drive the end-to-end investigation processes within a regulated environment. This role will ensure timely compliant and effective resolution of quality events while providing strong project management oversight.The selected candidate will be responsible for man...
Specialist Qa 35327 Juncos 500pm-530am
Integrated Services For Productivity & Validation, Inc
Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...
Qa Specialist 35269
Integrated Services For Productivity & Validation, Inc
Quality Professional with experience in Quality System and addition some knowledge or to be familiar with in PASx/MES application MAXIMO SAP LIMS QMTS and Veeva. Available during weekends and holidays as requested always available to be on site. RequirementsDoctorate OR Masters 2 years of experien...
Director Of Qa
Xsolla
ABOUT YOUThe Director of QA is a senior technical leadership role responsible for owning and scaling Xsollas quality engineering function across multiple product lines teams and time zones. You will define and drive the strategic vision for quality assurance from test automation architecture and CI...
Qa Specialist Shft 5 Pm To 530 Am 35165
Integrated Services For Productivity & Validation, Inc
Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...