EMMA International

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We are #hiring! We are looking for an experienced medical device QA/RA professional to join our team! - This is a fully onsite position, candidate must be willing to travel or commute to client site. - Demonstrated experience with Remediation Projects and FDA Enforcement Actions is required. - This is an IMMEDIATE hiring need, only candidates with immediate availability will be considered. Contact careers@emmainternational.com for more information.

The pharmaceutical industry is highly regulated, ensuring that all drugs are safe, effective, and properly labeled. One of the key components in this regulatory framework is the National Drug Code (NDC). Understanding what an NDC labeler code is and how it fits into the broader context of drug compliance is essential for anyone involved in the pharmaceutical sector. Read more here: https://lnkd.in/e5vG9mpA

Did you know that EMMA International's Staff Augmentation service extends beyond traditional QA/RA roles? Understanding that success in the life sciences industry demands a multifaceted approach, we offer expert personnel to support a wide array of functions essential to your organization's growth and operational efficiency including: ✅ Engineering Roles ✅ R&D Scientists and Engineers ✅ Manufacturing & Supply Chain Roles ✅ Quality Control (QC) and Laboratory Support .... and more! Are you ready to Discover The Advantage of Expertise? Learn more here: https://lnkd.in/gxCHezBs

EMMA International's engineering services are tailored to help you bring cutting-edge products to the market efficiently and effectively. With a team of seasoned engineers and industry experts, we provide comprehensive solutions that drive progress and ensure compliance at every stage. Learn more here: https://lnkd.in/ecZicE92

The Global Medical Device Nomenclature (GMDN) codes are a comprehensive and standardized system used to identify and classify medical devices. GMDN codes are developed and maintained by the GMDN Agency, with the aim of providing a universal language that simplifies the regulatory and communication processes within the healthcare industry. Read the blog here: https://lnkd.in/ezYDWvrN

Any guesses where members of our technical team are today? #EMMAOnTheRoad #LifeAtEMMA

In the pharmaceutical industry, the terms “drug substance” and “drug product” are frequently used, yet they refer to distinct entities in the drug development and manufacturing process. Understanding the difference between these two concepts is crucial for anyone involved in pharmaceuticals, whether they are in research, manufacturing, regulatory affairs, or quality assurance. In this blog, we’ll delve into the definitions, roles, and distinctions between drug substance vs drug product. Read more here: https://lnkd.in/eZ9m3hUQ

The EMMA team is hitting the road today for a client visit. As consultants we spend a lot of time on the road (or in the air), what are your travel day essentials? #LifeAtEMMA #EMMAOnTheRoad #ConsultantLife

With expertise in regulatory, quality, and compliance, as well as operations and clinical services, EMMA International is your single-source consulting solution. Discover more here: https://lnkd.in/eJgsWGAm