David Rodriguez Email & Phone Number

Adelaide, Sa, Au

Adelaide, Australia

Adelaide, South Australia, Australia

• Ensuring Adherence to local ISO17025 / ISO9001 certification.• Performing investigation of quality issues identified within the laboratories.• Preparing for and undertaking of system and method audits according to guidelines outlined in the Quality procedures and manuals.• Generating and reviewing risk assessments and data, following up on issues including CAPAs, and investigation of incidents.• Training of laboratory staff to ensure quality and competency.• Writing up new… Show more • Ensuring Adherence to local ISO17025 / ISO9001 certification.• Performing investigation of quality issues identified within the laboratories.• Preparing for and undertaking of system and method audits according to guidelines outlined in the Quality procedures and manuals.• Generating and reviewing risk assessments and data, following up on issues including CAPAs, and investigation of incidents.• Training of laboratory staff to ensure quality and competency.• Writing up new work orders according to client requests ensuring analytical and preparation methods as well as pricing are correct.• Creating and maintaining the Client profile templates and managing client’s database.• Liaising with other staff to obtain and follow up on turnaround times to communicate clients. Show less

Adelaide, South Australia, Australia

• Scanning, handling and processing samples upon arrival at the Laboratory facilities.• Preparing samples according to client requirements such as drying, breaking, crushing, splitting, sieving, pulverising, among other following company policies and procedures.• Reporting any changes on samples that could have an impact on the sample preparation process.• Performing QC’s analysis in samples after pulverizing process.• Shipping of samples that comply with the minimum… Show more • Scanning, handling and processing samples upon arrival at the Laboratory facilities.• Preparing samples according to client requirements such as drying, breaking, crushing, splitting, sieving, pulverising, among other following company policies and procedures.• Reporting any changes on samples that could have an impact on the sample preparation process.• Performing QC’s analysis in samples after pulverizing process.• Shipping of samples that comply with the minimum requirements to be analysed by the corresponding laboratory. Show less

Melbourne, Victoria, Australia

• Developing of SOPs of the packaging process of +250 products, in order to minimise errors during the whole process to obtain a final product with high-quality standards.• Ensuring that documentation complies to all WHS & Environmental policies and procedures.• Providing assistance to QA officers and manager in performing analysis to samples in order to approve them according to specifications.• Complying with all aspects of food quality systems, policies, and processes while… Show more • Developing of SOPs of the packaging process of +250 products, in order to minimise errors during the whole process to obtain a final product with high-quality standards.• Ensuring that documentation complies to all WHS & Environmental policies and procedures.• Providing assistance to QA officers and manager in performing analysis to samples in order to approve them according to specifications.• Complying with all aspects of food quality systems, policies, and processes while developing new procedures, methods, and work instructions related to the department. Show less

Bogota, D.C., Capital District, Colombia

• Contributing to the continuous development and maintenance of the quality management system (QMS), including writing and reviewing documents such as SOPs, protocols, reports, specifications and risk assessments.• Conducting release activities for Raw and packaging materials as well as intermediates and finished products.• Performing investigations on laboratory incidents using Root Cause Analysis tools such as the fishbone diagram and the 5 whys.• Ensuring GMP personnel and… Show more • Contributing to the continuous development and maintenance of the quality management system (QMS), including writing and reviewing documents such as SOPs, protocols, reports, specifications and risk assessments.• Conducting release activities for Raw and packaging materials as well as intermediates and finished products.• Performing investigations on laboratory incidents using Root Cause Analysis tools such as the fishbone diagram and the 5 whys.• Ensuring GMP personnel and processes adhere to GMP, QMS procedures and relevant legislations/guidelines.• Assisting with the preparation of Product quality reviews and CAPAs that derivate from such reviews. Show less

Bogota, D.C., Capital District, Colombia

• Providing support to the R&D department developing robust analytical methods using HPLC, UPLC to characterise new molecules and the identification of process impurities.• Preparing the schedule of preventive calibration for equipment to guarantee the correct function of the laboratory.• Contributing to the continuous development and maintenance of the quality management system (QMS), including writing and reviewing documents such as SOPs, protocols, and reports.• Conducting… Show more • Providing support to the R&D department developing robust analytical methods using HPLC, UPLC to characterise new molecules and the identification of process impurities.• Preparing the schedule of preventive calibration for equipment to guarantee the correct function of the laboratory.• Contributing to the continuous development and maintenance of the quality management system (QMS), including writing and reviewing documents such as SOPs, protocols, and reports.• Conducting Internal audits to be prepared for GMP and compliance accreditation requirements. Show less

Bogota, D.C., Capital District, Colombia

• Performing a range of analytical testing in raw material, packaging materials, batch testing and shelf-life testing according to ISO 9001 and ISO/IEC 17025 standards.• Supporting calibration and maintenance of +15 equipment and ensuring day to day cleanliness.• Performing analytical testing using conventional and modern technologies.• Complying with NATA/ISO 17025 accreditation requirements, including quality control procedures, assisting with the preparation of such… Show more • Performing a range of analytical testing in raw material, packaging materials, batch testing and shelf-life testing according to ISO 9001 and ISO/IEC 17025 standards.• Supporting calibration and maintenance of +15 equipment and ensuring day to day cleanliness.• Performing analytical testing using conventional and modern technologies.• Complying with NATA/ISO 17025 accreditation requirements, including quality control procedures, assisting with the preparation of such procedures.• Performing investigations and troubleshooting on systems and processes as required if atypical results were obtained.• Establishing testing methods and relevant SOPs as required to determine product quality using techniques such as HPLC, UV, TLC, dissolution and routine analysis• Writing of weekly reports and keeping accurate records, and data to keep evidence of the analysis. Show less

Advanced Diploma Of Leadership And Management

Graduate Diploma In Hseq

Bachelor Of Pharmaceutical Sciences

Diploma In Leadership And Management, Organizational Leadership