Peter Luk Email & Phone Number

Elizabeth, NJ

Testing of stability and finish products under USP and compendium guidelines

Rahway, New Jersey

Method Development, method validation, method optimization.

Massena, New York

Allendale, New Jersey

Wrote protocols, IQ, OQ, PQ, and SOP for various laboratory equipment.

Lancaster Area, Pennsylvania

Method optimization, Method Validation, SOP reviews, Method Development, Cleaning Validation

Parsippany, New Jersey

Methods validation, product development, process validation, stability testing, content and blend uniformity.

Rocky Mount, North Carolina Area

Document checking, Methods update, analyst mentoring

Princeton, New Jersey

TOC, raw material testing

Exton, Pennslyvania

Involved in Method Development and formulations of ophthalmic solutions and APIs within phase 1, 2, 3 of clinical research. Responsible for R&D of APIs. Validated new drug products, trend analysis of APIs, and evaluate efficacy of NPDs. Responsible for storage and collection of stability products for analysis. Performed assays, impurity analysis, FTIR.

Morris Plains, New Jersey

Involved in the method validation and method development of liquid dosage forms for Visine products line using HPLC with differential refractometerKnowledgeable in ICH, USP/NF, and cGMP guidelinesPresented data reports and trend analysis on current projectsInvolved in the method development and method validation of Listerine, Rolaids, and Sudafed for.

Involved in testing of solid dosage forms and HPLC troubleshootingMethod optimization of over the counter drugs in dissolution and assay methods.Participated in notebook review and auditsPerformed assays, impurity analysis, content uniformity, dissolution, cleaning validations, blend uniformity, and pH meter calibrations

Annually trained in cGMPs and 211 CFR. Involved in testing of liquid dosage forms (liquids, creams, topical solutions, and ointments)Performed testing includes stability samples, finished products, complaint samples, process validation samples, and engineering studiesOther responsibilities include investigation reporting, sample storage monitoring.

Whippany, New Jersey

Annually trained in cGMPs and 211 CFR. Involved in testing of raw materials, in process samples, stability samples, and solid dosage forms, investigation reporting, control substance reconciliation, and pH meter calibrations. Trained analyst and checked analyst's paperworkPerformed HPLC analysis, impurity analysis (HPLC and TLC), wet chemistry analysis.

Facility Closed)Annually trained in cGMPs. Involved in testing of raw materials and stability samples, SOP writing, instrument and equipment validation, methods development, and methods validationInvolved in the monitoring of sample storage for stability profilesPerformed HPLC impurity analysis, melting point analysis, and wet chemistry analysisWrote.

East Hanover, New Jersey

Annually trained in cGMPs and 211 CFRInvolved in testing of raw materials and in process materials, control substance reconciliation, and supplier validationPerformed wet chemistry analysis, FTIR, HPLC and GC analysis, titrimetric and potentiometric titration, particle size analysis, surface area analysis, TLC analysis, DSC analysis, TGA analysis, cold.

Parsippany, New Jersey

Annually trained in cGMPsInvolved in testing of raw materials, in process materials, stability samples, and solid dosage formsPerformed dissolution, content uniformity, FTIR, HPLC and GC analysis, titrimetric titration, nitrogen analysis, and water validation

Elizabeth, New Jersey

Facility closed/relocated)Trained in cGMPsInvolved in testing of raw materials and in process materialsPerformed wet chemistry analysis, FTIR, titrimetric and potentiometric titration, cleaning validation, content uniformity, HPLC analysis, and AA analysis