. You are responsible for regulatory compliance, and special projects and/or assignments. As the Associate Team Leader, you support the Team... following motions: bending, twisting, squatting, and reaching Exposure to FDA approved cleaning chemicals Exposure...
) to receive an alert: × Select how often (in days) to receive an alert: Associate Director - Regulatory Affairs... FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved...
about. Job Summary We are seeking an experienced Research Associate II to join our Insourcing Solutions team, located in San Diego, CA.... As the Research Associate II, you will conduct in vivo study work in rodents for multiple clients to support research...
are reported to be in shortage, according to industry and FDA reports. “Race to the bottom” pricing of mostly sterile injectable... more than $55 for a pack of five pens. Learn more about Civica’s plans and progress at Position Summary The Associate...
Summary & Responsibilities: The Associate Principal Engineer, Reagent Engineering will work within the Reagent Engineering.... Ability to collaborate professionally in a cross-functional team environment. Knowledge of FDA/ISO regulations and equipment validation...
about. Job Summary A Biostatistics Associate is responsible for verifying that the appropriate statistical methods are applied.... Familiarity with FDA/ICH guidelines/guidance and procedures, preferred. Ability to communicate verbally and in writing...
strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR... Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory advice on advertising...
Linde Gas & Equipment Inc Quality Assurance Associate Location: Cudahy, CA The Quality Assurance Specialist... products performed in accordance with FDA’s applicable regulations and LINDE’s standard operating procedures. The Quality...
. This Quality Associate II position will lead cross-functional teams as a Field Action (FA) Owner to facilitate the execution... industry Knowledge and understanding of regulations and standards (e.g. ISO9001, ISO13485, FDA 21CFR Parts...
Associate Summary: Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training... of product. Quality Systems Associate Assist the Quality Systems Manager to ensure center training programs follow procedural...
Linde Gas & Equipment Inc Quality Assurance Associate Location: Cudahy, CA The Quality Assurance Specialist... products performed in accordance with FDA’s applicable regulations and LINDE’s standard operating procedures. The Quality...
about. Job Summary We are seeking a Medical Technologist Associate to work in the Bacteriology Department at our Wilmington... worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We’re committed...
, GLPs, SOPs, USP and FDA guidelines. Responsibilities: Essential Duties Performs routine laboratory analysis... Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. Performs routine...
*This Position is onsite in Ridgefield, CT* Currently seeking a Clinical Associate (CA) to join our Study Management... and Responsibilities The Clinical Associate supporting Clinical Operations may perform the following tasks, but not limited...
Job Description Whole Foods Market is seeking a Seafood Associate Team Leader (Assistant Department Manager). This role... and reaching. Exposure to FDA approved cleaning chemicals. Exposure to temperatures: 32 degrees Fahrenheit (freezing), 32-40...
and FDA guidelines. Responsibilities: Essential Duties Performs routine laboratory analysis of In-Process, finished product..., TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. Performs routine qualification...
As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange..., FDA regulations, pharma regulations/compliant practices, and OIG guidelines. Additional requirements: Residency in the...
We're hiring Associate III, Manufacturing roles to support cGMP downstream manufacturing process for our pharmaceutical... annually. The Associate III, Manufacturing is responsible for supporting the overall cGMP downstream manufacturing process...
As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange..., FDA regulations, pharma regulations/compliant practices, and OIG guidelines. Additional requirements: Residency in the...
in this evolving industry. We are seeking an Associate Director of CDM to lead clinical data management activities... knowledge of regulatory guidelines (FDA/CFR, ICH/GCP), CDISC standards and eCTD submission requirements Excellent communication...