Julia Goldberg Email & Phone Number

Traverse City, MI, US

Gainesville, FL, US

Belgrade, MT, US

San Diego, CA, US

Within this role, I authored global procedures for complaint handling and medical device and tissue reporting in compliance with 21 CFR 803 and Part 1271 as well as regulatory reporting requirements per EU MDR 2017/745, MEDDEV 2.12-1, TGA, ANVISA, and other global Competent Authorities.Additionally, I created guidance documents to aid in reportability.

Within this role, I provided quality assurance support for new product development (NPI) and post market teams to ensure compliance with ISO, QSR, and global regulations. I evaluated Post Market Surveillance Data, authored PMSRs/PSURs, and drove updates to FMEAs and Risk Files with applicable data, per ISO 14971.I took ownership of the Post Market.

Warsaw, Indiana, US

Within this role, I performed all the functions of my prior title in addition to providing managerial guidance to a team of nine (9) individuals that performed complaint management and regulatory reporting activities.

Warsaw, Indiana, US

Within this role, I performed several different functions all focused on compliance to regulatory requirements per the Code of Federal Requirements Title 21 parts 803 and 820, part 1271, part 809, ISO 13485, EU MDD and MDR/IVDR, and global regulations governing medical devices, tissue products, combination devices, diagnostic tests (IVD), and software as a.

Las Vegas, Nevada, US

Within this role, I developed standard operating procedures for the manufacture of small-scale formulations.Further, I developed and implemented a quality process for environmental monitoring and controls of the manufacturing space using statistical test methods for in-process monitoring and of final packaged product.I developed statistically relevant test.

Las Vegas, Nevada, US

Within this role, I performed quality control analysis on product manufactured by outside vendors to verify that the proper specifications had been met. I performed small‐scale tests on chemical composition to observe changes in viscosity, solubility, and solution homogeneity. I performed data analysis on these changes to optimize the product formulation.I.

I worked in the Medical Biofilms Lab at the Center for Biofilm Engineering. During my time there I researched microbial control practices for a variety of medical issues. I primarily focused on a project that involved quality testing of a biofilm removal device on biofilm cultures of Pseudomonas aeruginosa 215. The project involved growing the biofilm.

Fort Worth, Texas, US

I worked to meet the needs of numerous customers in high volume situations. This involved answering questions about the product and utilizing upselling techniques. I used a POS system to perform the transactions and promoted the store charge card. I processed freight and organized inventory both on the sales floor and in back stock. I worked to promote a.

Leawood, KS, US

I sold tickets to high volumes of customers efficiently and accurately. I prepared concessions using sanitary methods and sold them to customers using a POS system. I organized inventory and used upselling techniques in all transactions. I maintained positive interactions with customers and coworkers in busy and high stress conditions.