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Anywhere, Everywhere

Leisurely sharing travel knowledge, information, and tips to others from joyful travel experiences.Where the best places are depending on the travel experience you're looking for.When the best times are to travel to a particular destination.Know the secrets and ways to save money on all travel costs.And much more . . . .

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“Here when YOU need help WRITE now”TMI am a traveling freelance writer/editor. Whether you are within my current location or in a remote place, we can work together to accomplish your writing or editing projects.

Thousand Oaks, Ca (Hq)

Managed projects for Small Molecules at different stages of drug development. Central point of contact for specific products under Stability programs and protocols.

Thousand Oaks, Ca (Hq)

Oversee day-to-day operations of QAL Chemistry Instrumentation department at the company headquarters. In-charge of other Chemists at different levels of technical expertise. Recognizing each of their unique strengths, help match best fit to allow them to maximize their individual contribution to the team, and overall, to the company.Ensure cGMP compliance as mandated by the US Food and Drug Administration (FDA). Conducted root cause analyses associated with non-conformance deviations (NC). Implemented corrective and preventive actions (CAPA). Ensure alignment of lab pratices and instrumentation technologies in QAL Chemistry Instrumentation departments across Global company sites. Spearheaded introduction and purchase of latest and greatest instruments available (NIR, FTIR, GC, Karl Fischer, etc.) to ensure company kept abreast with ever changing technological advancements in the world of qualitative analytical chemistry.Interacted with and presented to FDA inspectors during scheduled and unscheduled regulatory compliance audits.Audited/Evaluated Contract Testing laboratories to ensure their capability and cGMP compliance

Thousand Oaks, Ca (Hq)

Quality Control laboratory analyses of all raw materials used in various stages of clinical and commercial manufacturing processes in biologics, adhering to cGMP standards as mandated by the US Food and Drug Administration (FDA). Performed analyses using USP, NF, FCC, BP, European, and Japanese Pharmacopeia compendia standards.Performed analyses using Fourier Transform Infrared Spectroscopy (FTIR), Atomic Absorption Spectrophotometer (AAS), UV-VIS Spectrophotometer, HPLC, Gas Chromatography (GC), Karl Fischer, etc. Involved in instrument performance validations, as well as laboratory method validations as mandated by the US FDA. Active role in the initiation, revision, and review of analytical methods and Standard Operating Procedures (SOPs).Provided training to other associates on new lab instrumentations as well as analytical methods,

North Hollywood, Ca

Cross functional duties overseeing Manufacturing, Quality Control, and Calibration of radioactive isotopes for uses in Academia Research as well as in Nuclear Medicine.

Burbank, Ca

Company was later acquired by Eckert & ZieglerManufacture of wide array of radioactive isotopes for a broad range of uses in Academia studies and Research, and in Nuclear Medicine.Worked in a team of two responsible for procurement and purification of all radioactive materials prior to use in production.

Sunnyvale, Ca

Quality Control testing of Chromatography Columns for worldwide leader in HPLC systems manufacturer.

Bachelor Of Science, Chemistry

Creative Writing