lives. Read more: . PURPOSE AND SCOPE OF POSITION: The Associate Director, CTF Digital Plant IT Quality at Devens Cell..., Skills, and Abilities Thorough knowledge of regulatory computer system validation requirements including FDA, EMA...
products that match the ever-changing lifestyles and needs of people and families everywhere. JOB SUMMARY: The Associate... party logistics provider in Clayton, IN. The Associate Supervisor will ensure Good Manufacturing Practices (GMP) compliance...
on , , , , and . Job Description As an Associate Director of Regulatory Affairs in Chemistry, Manufacturing, and Controls (CMC), you will collaborate... agencies, such as the FDA, to ensure alignment on CMC matters. Responsibilities Include: Prepares CMC regulatory product...
We are seeking a highly skilled and experienced GMP Manufacturing Associate specializing in cell culture and downstream..., including FDA and EMA guidelines. · Excellent problem-solving and analytical skills, with the ability to troubleshoot...
is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial... to ensure the availability of materials for all Work Orders. The Inventory Control Associate will follow all inventory processes...
a promising future. Responsibilities: We currently have a great opportunity for a Production Associate. The Production... Associate position has the primary function of manufacturing reagents in conformance with established SOP's and cGMP. The main...
Job Title: Quality Lab Associate III - Chemistry Conduct chemical, biochemical and physical analyses... as mentor to other Quality Laboratory positions. Provide training and work direction for Quality Laboratory Associate I and II...
. As the SOGP establishes itself as Johns Hopkins' newest academic division, the Senior Associate Dean must embrace the... at the contact information below: Chanel Smith, Senior Associate- Vickie Antolini, Senior Client Partner Ken Kring...
SUMMARY The primary purpose of the Clinical Cell Therapy associate position is to assist in the performance of complex..., quality assurance and Directors. Perform procedures and maintain accurate documentation in compliance with FDA’s Good...
lives. Read more: . Title: Clinical Manufacturing Associate, CAR-T Location: Warren, NJ The purpose of the Clinical... Manufacturing Associate, CAR-T role is to manufacture human blood derived cell therapies per Standard Operating Procedures (SOPs...
Job Title: Clinical Trial Associate Location: Van Nuys, Los Angeles Job Type: Full-Time Overview: We are seeking... a highly organized and detail-oriented Clinical Trial Associate to join our team. This is a great opportunity for clinical...
groups (e.g., FDA, NIH) for effective execution of trials/studies. Drive stakeholder meetings for assigned trials/studies... estimate of the current salary range is $86,320 - $154,960 per year for the role of Lead-Clinical Research Associate or Lead...
School Diploma. A minimum of 1 year experience in a FDA regulated industry. Medical Device or Pharmaceutical preferred.... Working knowledge of ISO 13485 and 21CFR820. Internal audit experience preferred. Associate Degree in technical or quality...
The Office of the Vice President and General Counsel at Johns Hopkins University is seeking an Associate General... including legal hold management, discovery, motions practice, arbitration, and trials. Additionally, the Associate General...
: We are seeking a Senior Clinical Research Associate to join our clinical team in its mission to improve lives through medical... in accordance with Cutera SOPs, FDA regulations, ICH Good Clinical Practice (GCP) guidelines and other applicable regulations...
is seeking an Operations Associate to support invoicing, customer support, relationship management..., oncology professional societies, patient advocacy organizations, as well as federal agencies, including NIH, NCI, and FDA...
associate performs payables, receivables, and inventory tasks for the grain, oilseeds, and biofuels platforms of the company... Maintains all records associated with the execution function Interacts with government entities (USDA, FDA, FGIS, ect...
Summary The Clinical Research Associate will support all clinical research activities and all regulatory activities... and monitoring research data, and assisting with all institutional and governmental regulatory tasks. The Clinical Research Associate...
Title: Associate Director Human Factors and Usability Engineering Location: Cambridge, MA About the... and bring hope to patients and their families. Your job, as Associate Director Human Factors and Usability Engineering...
Title: Pharmaceutical Labeling Specialist(Associate) Location: Millsboro, DE 19966 (Hybrid; 3 days onsite... with Tuesday and Wednesday fixed onsite) Duration: 12 Months Job Description Minimum Education: Associate degree. Preferred...