qc - csv (hplc/gc)

Job Title and Industry Job Title: Benchtop IT / CSV Engineer – QC Laboratory Systems Industry: Life Sciences / Pharmaceutical Manufacturing Role Overview We are seeking a Benchtop IT / CSV Engineer to support validation and compliance activities for laboratory computerized systems and instruments used in QC and analytical environments. The role involves...

Role OverviewWe are seeking a QC Engineer with strong experience in Computer System Validation (CSV) for analytical laboratory instruments /equipment. The role ensures compliance with 21 CFR Part 11, data integrity, and global validation standards in a regulated GMP environment.Key ResponsibilitiesLead CSV activities for analytical equipment or instruments...

We are looking for a QC Engineer to support validation of analytical laboratory instruments and computerized systems in a GMP-regulated environment. The role focuses on ensuring compliance with 21 CFR Part 11, Annex 11, ALCOA+ principles, and data integrity requirements.Key ResponsibilitiesPlan, execute, and document qualification/validation of analytical...

Management of test samples: In-process and release samples, environmental testing samples and drug substance and excipient samples - Stability sample management. - Regulatory retain sample management. - Reference sample management - Responsible for QC instrument and equipment management, like C type instruments including HPLC, GC, IC and LC-MS and B type...

**Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and CSV system) - Responsible for overseeing execution of but not limited to IQ, OQ, PQ and ERES Test Scripts of QC laboratory equipment (lab...

Overview Support Computer System Validation (CSV) activities for QC lab systems, including benchtop instruments and associated software (e.g., Empower, LabX, Chromeleon, LabSolutions, etc.). Responsibilities Develop and execute IQ, OQ, PQ protocols, test scripts, and validation reports in line with site and corporate procedures. Prepare and maintain...

Roles & Responsibilities Support Computer System Validation (CSV)activities for QC lab systems, including benchtop instruments and associated software (e.g., Empower, LabX, Chromeleon, LabSolutions, etc.).Develop and execute IQ, OQ, PQ protocols, test scripts, and validation reports in line with site and corporate procedures.Prepare and maintain validation...

Management of test samples: In-process and release samples, environmental testing samples and drug substance and excipient samples - Stability sample management. - Regulatory retain sample management. - Reference sample management - Responsible for QC instrument and equipment management, like C type instruments including HPLC, GC, IC and LC-MS and B type...

Responsibilities Management of test samples: In-process and release samples, environmental testing samples and drug substance and excipient samples Stability sample management. Regulatory retain sample management. Reference sample management Responsible for QC instrument and equipment management, like C type instruments including HPLC, GC, IC and LC-MS and B...

Job Summary Perform sample management, including but not limited to: Managing in-process and release samples for product, environmental, and raw material management. Stability sample management. Regulatory retaining of sample management. Reference sample management. Assist in QC instrument and equipment management, such as C-type instruments including HPLC,...