Summary of Qualifications:

Over ** years of experience in a pharmaceutical environment

Adept in FDA, GMP, and ISO standards and regulations

Experience operating sit-down propane forklift

Experience entering correct specifications for work orders into an Automatic Batch Records system

Experience generating requisitions and associated labels and procedural instructions

Proficient in Microsoft Word, Excel, Access, and PowerPoint

Experience:

Vero Biotech LLC May 2021 – Present

QA Tech 2, Atlanta, GA

Inspects controlled raw materials, components and accessories at the receiving inspection area.

Performs QA release, and AQL verifications.

Identifies non-conformances and ensures the appropriate personnel initiate investigations.

Clearly communicates issues to management.

Coordinate calibration of all inspection and test equipment to assure no delays in releasing received items.

Maintains knowledge of all procedures and changes to specifications related to areas of responsibilities.

Sampling, and inventory quarantined items.

Inspection and testing of circuit boards, cables, and box builds.

Upkeep of files and documentation.

Perform other various duties as assigned.

MIMEDX July 2019 – May 2021

Lab Aide, Town Park, Kennesaw, GA

Transports laboratory materials and/or specimens to and from other laboratories, as required.

Prepares standard equipment, facilities, and/or solutions for laboratory experiments, in accordance with detailed procedures and instructions.

Cleans, breaks down, and stores laboratory equipment, facilities, and supplies after completion of laboratory exercises, as required.

Practices safety, environmental, and/or infection control methods.

Performs miscellaneous job-related duties as assigned.

IMMUCOR, INC. March 2019 – July 2019

Solid Phase Technician, Norcross, GA

Prepare reagents as bulk and for use in manufacturing processes

Verify that products are produced and labeled accurately

Follow appropriate control measures to prevent mixing of dissimilar solid phase components or products

Accurately calculate solid phase components used, rejected or returned

Perform department and equipment maintenance as well as calibration and environmental monitoring according to applicable procedures

Follow FDA regulations and ISO standards applicable to department operations and consequences of non-conformance

Participate in the training of new employees

Q2 SOLUTIONS July 2018 - March 2019

Clinical Trials Materials in QLIMS, Marietta, GA

Generate requisitions and associated labels and procedural instructions

Monitor work orders in laboratory information system (QLIMS). Print in order of priority to meet client's deadline.

Generate requisitions and associated labels and procedural instructions.

Ensure all validation kit orders are prioritized and run swiftly through clinical trials materials (CTM) checking system.

Maintain printer maintenance log, recording, identifying and reporting any faults that occur. Coordinate with relevant/supplier/contractor noticeable repairs to any broken equipment.

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