Jorge Torres Email & Phone Number

Connecticut, United States

Fargo, North Dakota, United States

• Ensure stability-related standard procedures are established, implemented, and continuously improved to ensure cGMP compliance with regulations and internal procedures in the context of stability testing.• Lead continuous systems improvements (procedures and systems) to improve organization effectiveness and ensure compliance.• Lead Quality Events, OOS investigations, or OOT investigations for stability samples.• Assure the Stability Chambers are appropriately operating within the intended use.• Ensures strong interaction with multiple groups to facilitate appropriate resource allocation and scheduling stability testing, outsourced testing, sample management, and internal initiative projects.• Prepare stability sections for health authority filings and annual product quality reports. Author and review applicable stability sections of Regulatory submissions. Collaborate with Regulatory Affairs, providing expert input to relevant sections of the dossier to ensure submission timelines and regulatory commitments are met.• Prepare stability metrics to support the Quarterly Quality System Management Review stability updates and regular updates to the Senior Executive Team (SET).• Provide guidance and support to inter-departments for developmental stability programs on new products, technical transfers, and change controls, ensuring that expectations are incorporated into stability strategies.• Develop, approve, facilitate execution, and oversee all global stability strategies based on regulatory requirements, internal procedures, technical information, and historical stability data.• Oversee and facilitate the execution of the established stability strategies across functional areas and internal and external sites, including stability study initiation, stability sample management, stability storage, and stability-related documentation (protocols. Summary reports and stability testing.

Columbia, South Carolina Area

Columbia, South Carolina Area

Columbia, South Carolina Area

Largo, Fl

• HPLC method development. • DEA regulated API testing. • USP and EP compendial testing. • Documentation following cGMP.

Altanta, Ga

• Operate, calibrate and troubleshoot instruments such as UV-Vis, FT-IR, GC, RVT and LVT Viscometer, pH meter, and HPLC. • Perform analysis on raw materials, in-process and finished goods. Documents all the analysis.• Follow cGMPs and GLPs.• Perform accelerated stability, shelf-life and compatibility studies on product samples.• Ensure and update the inventory of the QC lab. • Write, update and reinforce the compliance of the SOPs. • Work with the R&D department. • Develop and implement new Quality methods following the ISO system.• Lead OOS troubleshooting and investigations.

Daytona Beach, Florida

• Formulate sun care products utilizing emulsion techniques.• Perform advanced In-Vitro testing on products following national and international regulations.• Operate, calibrate/validate and troubleshoot instruments such as UV-Vis, FT-IR, GC/MS, RVT and LVT Viscometer, pH meter, Rheometer, PSA and HPLC. • Design and interpret crystallization and informal stability studies to verify quality and robustness of formulations.• Perform bench work on formulation and wet chemistry on raw materials.• Follow established SOP’s with little or no supervision. Follow cGMPs and GLPs. • Perform IQ and OQ to new instrumentation. • Dispose hazardous waste following environmental regulations.

Cocoa, Florida

• Responsible for performing routine/non-routine analysis for raw materials, in-process and finished products. • Perform bench work such as pH, viscosity, and specific gravity. • Perform titrations to determine water hardness, and acid value. • Perform data entry in batch records, laboratory log books, and reports regarding product quality. • Follow cGMPs and GLPs. • Prepare product validation reports, APR and Long Term Stability Control. • Prepare standards and sample solutions for HPLC testing. • Operate, calibrate and troubleshoot instruments such as pH meter, UV-Vis, FT-IR and HPLC. • Develop and implement new Quality methods following the ISO system.• Lead OOS troubleshooting and investigations. • Execute troubleshooting of analytical methods when needed.

San German, Puerto Rico

• Supervise the chemistry department’s computer laboratory. • Maintain inventory and provide lab materials throughout the chemistry department. • Write and modify laboratory procedures for General Chemistry laboratories. • Provide tutoring to students who needed it. • Assist Teacher's Assistant during laboratories courses. • Assist students with procedures, and instrumentation. • Disposed of raw materials and solutions following environmental regulations’ procedures.