Tara Florez Email & Phone Number

Bubendorf, Basel-Country, Switzerland

Allschwil, Basel-Country, Switzerland

- Developed and organized the company handbook, templates & policies.- Designed a lean and appropriate quality management system for compliancy.- Ensured that the developmental activities for projects remained on time and within budget.- Made sure ongoing pCMC activities were compliant to regulatory standards/ guidelines.- Consulted with peers to seamlessly bridge the drug discovery phase to preclinical phase for the company's lead molecule.- Executed a regulated electronic… Show more - Developed and organized the company handbook, templates & policies.- Designed a lean and appropriate quality management system for compliancy.- Ensured that the developmental activities for projects remained on time and within budget.- Made sure ongoing pCMC activities were compliant to regulatory standards/ guidelines.- Consulted with peers to seamlessly bridge the drug discovery phase to preclinical phase for the company's lead molecule.- Executed a regulated electronic laboratory notebook & data management system for bioanalytical in-vitro data integrity and management.- Deputy for CEO. Show less

Basel, Switzerland

- Orchestrated and directed a high-performing team of 3 laboratory associates in the physical chemical labs.- Streamlined processes and optimized workflows.- Lead & organized successful method verifications/validations/transfers into the QC physical-chemical laboratory.- Accountable for the management and lifecycle of raw and packaging materials (i.e., incoming good check to release).- Managed and liaised with CROs/CMOs to assure quality, budget and responsibilities for RM, DS… Show more - Orchestrated and directed a high-performing team of 3 laboratory associates in the physical chemical labs.- Streamlined processes and optimized workflows.- Lead & organized successful method verifications/validations/transfers into the QC physical-chemical laboratory.- Accountable for the management and lifecycle of raw and packaging materials (i.e., incoming good check to release).- Managed and liaised with CROs/CMOs to assure quality, budget and responsibilities for RM, DS or DP testing.- Attentively reviewed and/or approved various GMP documentation (i.e., Analytical Batch Records, plans and reports, specifications, and instrument calibrations).- Supported QA and contributed to quality investigations or changes within a regulated QMS infrastructure.- Deputy for the Head of QC. Show less

Basel Metropolitan Area

- Designed, planned, performed, interpreted, and reported results of dissolution rate experiments including bio relevant dissolution testing USP I, II and IV apparatuses, HPLC and UV spectrometer.- Adhered to project timelines for all assigned projects.- Ensured GMP compliance for all relevant analytical activities for various complex projects.- Provided raw data documentation, evaluation, and interpretation of scientific results with a high focus on quality and compliance.-… Show more - Designed, planned, performed, interpreted, and reported results of dissolution rate experiments including bio relevant dissolution testing USP I, II and IV apparatuses, HPLC and UV spectrometer.- Adhered to project timelines for all assigned projects.- Ensured GMP compliance for all relevant analytical activities for various complex projects.- Provided raw data documentation, evaluation, and interpretation of scientific results with a high focus on quality and compliance.- Collaborated & provided support with team members across the organization. Show less

Rahway, New Jersey, United States

Analytically supported late phase drug substance, including pilot plant operations.

Kenilworth/ Summit, New Jersey, United States

Kenilworth, New Jersey, United States