On December 8, 2021, Thermo Fisher Scientific completed the acquisition of PPD. Together, Thermo Fisher and PPD share the pursuit of a common goal: to enable customers to make the world healthier by accelerating the development of new medicines.

On December 8, 2021, Thermo Fisher Scientific completed the acquisition of PPD. Together, Thermo Fisher and PPD share the pursuit of a common goal: to enable customers to make the world healthier by accelerating the development of new medicines.

Develop analytical control methods in support of cannabis manufacturing specifically in support of New Product Initiatives and Development. Improve and streamline current methods and laboratory practices to improve quality, efficiency, and safety of environment. I also manage New Product and Accelerated Stability Programs as well as develop new formulations for expansion of Distillate Vape SKUs.

Responsible for routine in-process testing of API material in support of manufacturing multiple insulin molecules. Develop and optimize methods for migration from HPLC to UHPLC, and author investigations into OOS and atypical results. Ensure laboratory meets goals of sample throughput and turn around time stated in business agreements regarding release of verified data.

Perform analytical testing on raw material, in-process, finished product, and stability samples.

I am responsible for automating and maintaining laboratory instrumentation used in the high throughput screens for drug discovery in the Research Laboratories with the Quantitative Biology Team. Data analysis of assays reveals potential "hits" for early phase and pre-clinical trials.

Executing lyophilized cycles, analytical assays, instrument qualification/maintenance/validation associated with formulation and stability studies.Support internal QC with technical expertise and investigations of foreign particles and OOS data from plant manufacturing lines.

Authored, reviewed, and executed validation protocols, methods, and investigative reports in support of method qualification and transfer activities for numerous client projects and manufacturing.Trained over 20 Analysts on analytical methods and instrumentation in the Quality Control Labs.

Validated laboratory instrumentation in support of a lab construction and expansion. Maintained and qualified analytical instrumentation on regulated schedule.

Performed finished product, in-process, and stability testing in support of GMP manufacturing.

Maintained and repaired all analytical laboratory instruments, and managed history logs. Served as a resource to support client and regulatory audits. Identified and implemented a process improvement resulting in savings of over $25,000 to the company

Cleaned, maintained, and kept inventory of all laboratory glassware needed in support of GMP testing, and monitored all stability environmental chambers